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Tumor-associated macrophages in tumor metastasis: biological roles and clinical therapeutic applications


Tumor metastasis is a major contributor to the death of cancer patients. It is driven not only by the intrinsic alterations in tumor cells, but also by the implicated cross-talk between cancer cells and their altered microenvironment components. Tumor-associated macrophages (TAMs) are the key cells that create an immunosuppressive tumor microenvironment (TME) by producing cytokines, chemokines, growth factors, and triggering the inhibitory immune checkpoint proteins release in T cells. In doing so, TAMs exhibit important functions in facilitating a metastatic cascade of cancer cells and, meanwhile, provide multiple targets of certain checkpoint blockade immunotherapies for opposing tumor progression. In this article, we summarize the regulating networks of TAM polarization and the mechanisms underlying TAM-facilitated metastasis. Based on the overview of current experimental evidence dissecting the critical roles of TAMs in tumor metastasis, we discuss and prospect the potential applications of TAM-focused therapeutic strategies in clinical cancer treatment at present and in the future.


Metastasis is a process of tumor cells escaping from the primary sites, spreading through lymphatic and/or blood circulations and ultimately disseminating to the distant sites. As one of the hallmarks of cancer, development of metastasis accounts for more than 90% cancer-related deaths [1]. Usually, the metastasis of tumor cells is a multistep sequence mainly including (a) invasion in the primary sites, (b) intravasation into the vasculature, (c) survival in the circulations, (d) extravasation out of the vasculature, and (e) adaption and growth in the metastatic sites [2, 3]. Failure in any of those steps will prevent the formation of metastasis. In addition to the alterations of the intrinsic properties in tumor cells, the “seed and soil” concept, firstly proposed by Stephen Paget in 1889, has been widely accepted as a critical theory to do with metastasis [4]. In this theory, tumor cells themselves are not sufficient for the development of metastasis. In fact, both the tumor cells and multiple components of the tumor microenvironment (TME) and their complicated cross talk are closely involved [5, 6]. Macrophages populating in the surrounding TME are usually termed as tumor-associated macrophages (TAMs) [7, 8]. A large volume of studies suggests that TAMs serve as prominent metastasis promoters in the TME, which orchestrate almost all of the 5 cascade steps of tumor metastasis as mentioned above [9, 10]. By producing growth factors, proteolytic enzymes, and various inhibitory immune checkpoint proteins in T cells, TAMs display implicated functions in regulating metastasis. Also, targeting TAMs as therapeutic strategies to prevent tumor progression and metastasis has attracted more and more researchers’ attention in recent years. So far, different types of molecular agents against TAMs are emerging as potential anti-cancer approaches. This review aims to provide an overview of the origin, classification, and polarization of TAMs as well as the mechanisms underlying the TAM-induced metastasis. Also, we will specifically discuss the agents targeting TAMs for cancer therapy. It is hoped that this review will help readers to understand the roles of TAMs in metastasis and their potential in clinic therapeutic applications against tumor progression.

Overview: biological information and polarization of TAMs

The definition, origin, and functions of TAMs

Macrophages are a type of versatile immunocytes, executing a broad spectrum of functions that range from modulating tissue homeostasis, defensing against pathogens, and facilitating wound healing [11]. Macrophages infiltrating tumor tissues or populated in the microenvironment of solid tumors are defined as tumor-associated macrophages (TAMs). As a critical component of tumor microenvironment, TAMs affect tumor growth, tumor angiogenesis, immune regulation, metastasis, and chemoresistance. Most of the TAMs gather in the leading edge and avascular areas, while some others align along the abluminal side of the vessels as well [12, 13]. It is generally believed that the blood monocytes derived from bone marrow hematopoietic stem cells are the primary resource of macrophages [14,15,16]. However, recent evidence suggests that a majority of resident macrophages stem from yolk sac progenitors, which proliferate or differentiate in situ and have progeny throughout their life, such as alveolar macrophages, brain macrophages, and Kupffer cells [11, 17,18,19]. They are recruited and activated by various signals in the TME and then exhibit dramatic impacts on the tumor progression and metastasis. The cellular origin of macrophages and TAMs was shown in Fig. 1.

Fig. 1

Cellular origins and functions of TAMs. As the major primary resource of macrophages, monocytes are generated from hematopoietic stem cells (HSCs) that differentiate into granulocyte-macrophage progenitors (GMPs) and then into monocyte-dendritic cell progenitors (MDPs). Besides, tissue-resident macrophage stem from yolk sac progenitors are another key resources of macrophages, which proliferate or differentiate in situ, such as alveolar macrophages, brain macrophages, and Kupffer cells. The mature monocytes released in the blood and tissue-resident macrophages are recruited and activated by various signals in the TME and then exhibit dramatic impacts on the tumor initiation and promotion, metastasis, immune regulation and angiogenesis

Like macrophages perform diverse functions in immune regulation, TAMs also play multi-functional roles in tumor progression, including cancer initiation and promotion, immune regulation, metastasis, and angiogenesis, as shown in Fig. 1. For example, the presence of TAM-derived inflammatory cytokines interleukin (IL)-23 and IL-17 have been shown to trigger tumor-elicited inflammation, which in turn drives tumor growth [20] (Fig. 1). Another study demonstrated that the increased TAM-derived IL-6 exerts an amplifying effect on the inflammation response, thus promoting the occurrence and development of hepatocellular carcinoma via STAT3 signaling [21]. Moreover, TAMs acquire an M2-like phenotype, providing essential support on tumor progression and metastasis, despite their weak antigen presenting ability [22].

The classification and polarization of TAMs

It is clear that macrophages are capable of displaying very different and even opposing phenotypes, depending on the microenvironment they embedded in. Activated macrophages are often classified into M1 (classical-activated macrophages) and M2 (alternative-activated macrophages) phenotype [23] (Fig. 2). In general, M1 macrophages foster inflammation response against invading pathogens and tumor cells, whereas M2 macrophages tend to exert an immune suppressive phenotype, favoring tissue repair and tumor progression. These two types of macrophages are distinct in their different markers, metabolic characteristics, and gene expression profiles. M1 macrophages secrete proinflammatory cytokines such as IL-12, tumor necrosis factor (TNF)-α, CXCL-10, and interferon (IFN)-γ and produce high levels of nitric oxide synthase (NOS, an enzyme metabolizing arginine to the “killer” molecule nitric oxide), while M2 macrophages secrete anti-inflammatory cytokines such as IL-10, IL-13, and IL-4 and express abundant arginase-1, mannose receptor (MR, CD206), and scavenger receptors [24, 25] (Fig. 2). The conversion between M1 (anti-tumorigenesis) and M2 (pro-tumorigenesis) is a biological process named “macrophage polarization” in response to microenvironmental signals [26]. Though studies found that TAMs are able to exhibit either polarization phenotype, researchers tend to consider TAMs as M2-like phenotype-acquired macrophages [22, 26,27,28]. It is consistent with these clinical observations that the accumulation of macrophages in the TME is largely associated with worse disease outcome [13, 29]. However, classification and identification of TAMs should be correlated mainly to their function such as metastasis, angiogenesis, and immune regulation. Expression of CD68, CD14, HLA-DR, and CD204 have been used for macrophage classification, and other proteins such as MMP2/9, B7-H4, STAT-3, CD163, and CD206 have been used for classification of TAMs [30]. We have listed these characterized biomarkers, CDs, and cytokines for TAM identification in Table 1. To better understand the correlation between TAMs, metastasis, and clinical applications in cancer therapy, we will further characterize the molecular mechanisms underlying TAMs polarization from M1-like to M2-like in detail below, also as shown in Fig. 2.

Fig. 2

Tumor-associated macrophages (TAMs) polarization and its regulatory networks. Polarization of TAMs is regulated by multiple microenvironmental cytokines, growth factors, epigenetic regulators, and other signals derived from tumor and stromal cells. Two types of macrophages (M1/M2) secrete different immune markers, metabolic characteristics, and gene expression profiles to exert different functions

Table 1 Biomarkers associated with tumor-associated macrophages

Polarization of TAMs is regulated by multiple microenvironmental cytokines, chemokines, growth factors, and other signals derived from tumor and stromal cells [24]. Among those factors, colony stimulating factor 1 (CSF-1) and C-C motif ligand 2 (CCL2) are the most two well-documented macrophage recruiters and M2-stimulating factors (Fig. 2). CCL2 was earlier reported to shape macrophage polarization toward the protumor phenotype via the C-C chemokine receptor 2 (CCR2) expressed on the surface of macrophages [38]. Blocking the CCL2-CCR2 interaction either by genetic ablation or antibodies obviously inhibits metastatic seeding and prolongs the survival of tumor-bearing mice along with the diminished protumor cytokine expression [38,39,40]. Moreover, abundant clinicopathological data have verified the association between high concentrations of CCL2 in tumor with increased TAM infiltration and metastatic events [22, 39, 41]. CSF-1 is another potent determinant factor of macrophage polarization. CSF-1 wide overexpression is observed at the invasive edge of various tumors and correlates with a significant increase in metastasis [24]. In addition, tumor graft models showed that CSF-1 depletion led to greatly reduced macrophage density, delayed tumor progression, and severely inhibited metastasis [22, 24, 42, 43]. And the restoration of expression of CSF-1 in CSF-1 null mutant mice with xenografts accelerated both tumor progression and metastasis [42]. Vascular endothelial growth factor A (VEGF-A) has long been considered as a powerful pro-tumor factor [44]. Other than its pro-angiogenic effects, VEGF-A also fosters the malignant growth of tumors by inducing TAM infiltration and M2 polarization in the presence of IL-4 and IL-10 [45]. Direct evidence came from the gain-of-function experiments in the xenograft model of skin cancer, whereby VEGF-A upregulation rescued the clodronate induced macrophage depletion and resulted in shortened xenograft survival [45,46,47]. Besides, the overactivation of the epidermal growth factor receptor (EGFR) signaling pathway by either overexpression or mutation is frequently involved in tumor initiation, growth, and metastasis [48]. Actually, EGFR signaling not only promotes proliferation and invasiveness of tumor cells directly, but also adjusts the TME by regulating macrophage recruitment and M2-like polarization [49, 50]. Disrupted EGFR signaling by cetuximab or gene knockout resulted in less M2-polarized TAMs and correlated with better prognosis in colon cancer models of mice [51, 52]. Beyond those well-investigated factors mentioned above, a number of new homeostatic factors have been described as TAM inducers recently. For example, prostaglandin E2 (PGE2) synergized with CSF-1 to promote M2 polarization by transactivating the CSF-1R, and PGE2-elicited macrophage infiltration was significantly halted in the absence of CSF-1R [53]. In addition, CCN3 (also known as NOV, nephroblastoma overexpressed) led to enhanced M2 macrophage infiltration, whereas CCN3 deficiency prolonged xenograft survival in prostate cancer [54]. Furthermore, other chemokines such as IL-4, IL-6, IL-13, CCL7, CCL8, CCL9, CCL18, and CXCL12 are also highly expressed in tumors and involved in TAM recruitment and polarization [9, 10, 55,56,57] (Fig. 2).

Hypoxia, which resulted from tumor cells with a status of vigorous metabolism and rapid growth but poorly organized vasculature, is a common feature occurring in the majority of solid tumors [58]. Hypoxia promotes the malignant tumor behaviors by various mechanisms, such as inducing immune escape, promoting glycolysis, antagonizing apoptosis, promoting cell dedifferentiation, and reducing therapeutic effectiveness [59,60,61]. It is worth noting here that hypoxia also roles as a vital regulator of macrophages, which helps tumor cells overcome nutritive deprivation and convert the TME into more hospitable sites [28]. The gradients of chemokines induced by hypoxia, such as CCL2, CCL5, CSF-1, VEGF, semaphorin 3A (SEMA3A), endothelial cell monocyte-activating polypeptide-II (EMAP-II), endothelin, stromal cell-derived factor 1α (SDF1α), eotaxin, and oncostatin M, are responsible for the migration of TAMs into the hypoxic areas [28]. Hypoxia further traps the seeding macrophages by downregulating the chemokine receptors expressed on macrophages [62, 63]. Besides, hypoxia modulates the TAM phenotype toward a pro-tumoral profile by various factors. Lactate, massively produced by anaerobic glycolysis of tumor cells in oxygen-deprived areas, is one of the key inducers of M2 phenotype. It can be sensed by G protein-coupled receptor 132 (Gpr132), a membrane receptor on macrophages, which subsequently activates downstream signals and modulates the expression of polarization-associated genes [64]. And it has been shown that the enhanced expression of Gpr132 relates to the worse outcome of breast cancer patients, which was further verified by the positive association between the Gpr132 level and M2 macrophages infiltration, metastasis, and poor prognosis in breast cancer models in mice [64]. Similar stimulatory functions on macrophage accumulation and polarization can also be achieved by angiopoietin-2 (Ang-2), which is generally accepted as a regulator of vessel stabilization and growth in accompany with VEGF, Ang-1, via specifically binding to the receptor Tie-2 [65, 66] (Fig. 2). Ang-2 can also be dramatically upregulated by hypoxia [65]. However, there exists opposed evidence claiming that hypoxia is not the major driver of M1-M2 skewing [28, 67]. Instead of a direct effect on M2 transforming, hypoxia only fine-tunes hypoxia-regulated genes expression without influencing their M2 markers expression or the relative abundance of TAM subsets [67].

Epigenetic derangements is another universal feature in cancer. Epigenetic regulators reshape chromatin structures, pack the genome, and change gene expression patterns without altering the genome itself [68, 69]. More recently, a growing number of publications focus on the epigenetic participation in macrophage phenotypic switch [70, 71] (Fig. 2). Usually, most of the key points of epigenetic regulators are enzymes, which are druggable and easy to be translated into clinical applications for tumor intervention. For example, protein arginine methyltransferase 1 (PRMT1), SET and MYND domain-containing protein 3 (SMYD3), Jumonji domain-containing protein 3 (JMJD3), NAD-dependent protein deacetylase sirtuin-2 (SIRT), and bromodomain and extraterminal (BET) proteins positively regulate M2 polarization by upregulating M2 markers, while DNA methyltransferase 3b (DNMT3b), Jumonji domain-containing protein 1A (JMJD1A), histone deacetylase 3 (HDAC3), and HDAC 9 do the opposite effect [70, 71]. Interfering these epigenetic enzymes with pharmacologic modulators was able to prevent these macrophages from polarizing to M2 s and control the malignant progression of tumors.

As another type of epigenetic regulator, microRNAs (miRNAs) are also in control of macrophage polarization (Fig. 2). To date, miR-125, miR-155, miR-378, miR-9, miR-21, miR-146, miR-147, miR-187, miR-222, and miR-let7b have been reported as dominant TAM modulators [72]. For example, miR-222-3p, implicated as a tumor promoter in diverse tumor types, activates macrophages to the M2 phenotype by downregulating suppressor of cytokine signaling-3 (SOCS3) which is a negative feedback regulator of the JAK/STAT signaling pathway [73]. What is more, let-7b, enriched in prostatic TAMs, is drawing attention along the same line. Prostatic TAMs treated with let-7b inhibitors displayed characteristics of M1, with a significantly higher expression of pro-inflammatory cytokines (such as IL-10, IL-12, and IL-23), and downregulated pro-tumoral cytokines such as TNF-α [74].

Taken together, the polarization of TAMs is regulated by complicated biological networks (Fig. 2), which clinically correlates with cancer metastasis and progression.

Mechanisms underlying TAM-facilitated metastasis

As mentioned above, TAMs display lots of important biological functions in tumor progression from different aspects. Here, we mainly focus on the correlation between TAMs and tumor metastasis. In fact, how TAMs contribute to tumor metastasis is a puzzling question which enables researchers to pursue the answers for dozens of years, though the existing studies demonstrate that TAMs implicate in almost every step of metastasis as described below, also shown in Fig. 3.

Fig. 3

Mechanisms of tumor-associated macrophages (TAMs) in tumor metastasis. TAMs affect virtually almost every step of tumor cells metastasis, including invasion, vascularization, intravasation, extravasation, establishing pre-metastatic niches, and protecting circulating tumor cells survival

TAMs promote invasion of tumor cells

Metastasis begins with tumor cells obtaining the ability of invasiveness and escaping from the confines of the basement membrane into the surrounding stroma [5, 75]. Highly invasive tumor cells always share the characteristics of loss of intrinsic polarity and loosely attachment to the surrounding tissue structures [76]. Epithelial-mesenchymal transition (EMT) is a predominant event in this morphological transformation, which contributes to malignant biological properties including invasion and metastasis [76]. During EMT process, tumor cells lose cell-cell junctions and apical-basal polarity as a result of E-cadherin repression and acquire a motile mesenchymal cell phenotype [77, 78].

Recently, a number of studies suggested that TAMs involve in the regulation of EMT process [79,80,81]. Immunostaining of clinical hepatocellular carcinoma (HC) samples revealed that the EMT hotpots, such as the edge of tumor nests, are also the sites where TAMs infiltrate in abundance [80]. Moreover, co-cultured HC cell lines with TAMs enhanced the expression of N-cadherin and Snail, both of which are hallmarks of mesenchymal phenotypes. Meanwhile, E-cadherin was observed to be downregulated. This phenomena also occurred in gastric cancer and pancreatic ductal adenocarcinoma (PDAC) [82]. Biologically, macrophages participate in the EMT process via secreting various soluble factors, such as IL-1β, IL-8, TNF-α, and transforming growth factor-β (TGF-β) [80, 83, 84]. Extracellular matrix (ECM) serves as a scaffold as well as a barrier for tumor cell migration [85], of which degradation is a focal event in metastasis. It has been identified that TAMs are capable of secreting a number of proteolytic enzymes, including cathepsins, matrix metalloproteinases (MMPs, such as MMP7, MMP2, and MMP9), and serine proteases, which are important components mediating ECM degradation and cell-ECM interactions [86,87,88]. In addition, an earlier study demonstrated that M2 macrophage promotes the invasiveness of gastric and breast cancer cells by producing chitinase 3-like protein 1 (CHI3L1). CHI3L1 upregulates MMP expression via interacting with interleukin-13 receptor α2 (IL-13Rα2) chain which triggers the activation of the mitogen-activated protein kinase (MAPK) signaling pathway [89]. Once the tumor cells break away from the constraint of ECM networks, they would move toward the stimuli along with the ECM fiber by interacting with other ECM components, such as fibronectin and vitronectin [90, 91]. Furthermore, secreted protein acidic and rich in cysteine (SPARC) synthesized by TAMs were shown to be necessary for the migration of tumor cells, aside from its role as an ECM deposition regulator. According to the earlier studies, SPARC favors fibronectin and vitronectin interaction with tumor cells through integrins, generating a traction force along ECM fibers [92, 93]. The traction force pulls tumor cells to rapidly travel through the stroma like tram lines and guarantees the rapid motivation of cells within stroma as well as toward tumor vasculature since many of those ECM fibers terminally converge on blood vessels [90]. Genetic ablation of SPARC led to attenuated metastasis by decreased ECM deposition and impaired tumor cell-ECM interaction [90, 92, 93].

TAMs promote vascularization of tumor cells

Tumor vasculature serves as a major route for the metastasis of malignant tumors. When solid tumors grow up to a certain size, a process termed as “ angiogenic switch” will be turned on by various mechanisms to trigger a high-density vasculature for nutrients supply and wastes removal [94, 95]. TAMs are critical players in the regulation of “angiogenic switch.” They form clusters in the intra-tumoral regions and the invasive fronts, both of which are the hotspots of angiogenesis and metastasis. In contrast, the absence of TAMs significantly reduced the vessel density by 40% [96, 97]. In addition to affecting the formation of new tumor vessels, TAMs also stimulate the remodeling of the established vasculature to a more tortuous and leaky form in favor of tumor dissemination [96, 97]. In fact, researches strongly argue the important roles for VEGF and MMP-9 (plays a character in releasing VEGF from matrix) in regulating TAM-driven angiogenesis. Also, there are some other proangiogenic molecules involved as well, such as fibroblast growth factor (FGF)-2, CXCL8, IL-1, IL-8, cyclooxygenase (COX)-2, nitric oxides (iNOS), and MMP7 [96,97,98,99]. Furthermore, there is a novel subset of TAMs expressing tyrosine-protein kinase receptor Tie-2 (also known as angiopoietin-1 receptor) termed as TEMs [65, 100]. Experiments in a variety of tumor models clarify that TEMs were endowed with dramatic proangiogenic activity, since Tie-2 is capable of binding with all the known angiopoietins (Angs, including Ang-1, Ang-2, Ang-3, and Ang-4) [12, 65, 66]. Therefore, selective elimination of TEMs by a suicide gene strategy may be another promising option for preventing angiogenesis and tumor progression [66].

Besides, TAMs also account for lymphangiogenesis, an important route for tumor cells disseminating to regional lymph nodes and distant metastasis, in a VEGF-C (a ligand overexpressed by tumors)/VEGFR-3 (a receptor of VEGF-C expressed on the TAMs) axis-dependent manner. VEGF-C/VEGFR-3 axis fosters lymph angiogenesis either by directly affecting the lymphatic endothelial cells (LECs) activity or indirectly elevating the cathepsins secretion whose downstream molecular heparanase is a robust inducer of lymphangiogenesis [101,102,103]. From the mouse models, treatment with antibodies against VEGF-C/VEGFR-3 or genetic ablation of heparanase significantly altered the lymphatic vessel phenotype and subsequently impaired the primary tumor growth and metastasis [101].

Taken together, these evidences demonstrate that TAMs function in the way of promoting the vascularization of tumors via different pathways and thus are closely involved in tumor metastasis.

TAMs promote intravasation of tumor cells

Tumor cells squeezing through small pores in vascular endothelium to gain access to the host vasculature is another critical step in metastasis [104]. An experiment utilizing intravital multiphoton imaging gave a direct and kinetical visualization of intravasation. According to this experiment, an intravasating tumor cell is always visualized to be accompanied by a macrophage within one cell diameter, showing a direct evidence of TAMs involving in tumor cell intravasation [105, 106]. Consistently, clinical observations have identified the tripartite arrangement of TAMs, tumor cells, and endothelial cells as the tumor microenvironment of metastasis (TMEM). The TMEM is a predictor of increased hematogenous metastasis and poor prognosis, at least in breast cancer [107]. The mechanisms underlying this synergistic interaction are complicated. On the one hand, macrophages break down the ECM around the endothelium by a number of proteolytic enzymes such as cathepsins, matrix metalloproteinases, and serine proteases [86,87,88]. On the other hand, TAMs hijack tumor cells into the circulation by a positive feedback loop consisting of tumor cell-produced CSF-1 and TAM-produced EGF [108]. The former cytokine stimulates macrophage’s motility as well as EGF production, which in turn signals to tumor cells and mediates chemotactic migration toward blood vessels [108, 109]. Therefore, inhibition of either CSF-1 or EGF signaling pathway perturbs the migration of both cell types and reduces the numbers of circulating tumor cells as well.

TAMs promote tumor cell survival in the circulation

Once penetrated into the vasculature, the tumor cells have to be primed for survival and egress from the circulation. Clots packed around the tumor cells alleviate survival stress from such as natural killer (NK) cells in a tissue factor (TF)-dependent manner in the general circulation and capillaries [110, 111]. In fact, a strategy disrupting macrophage functions by genetic methods diminished the tumor cells survival in pulmonary capillaries and abrogated tumor invasion into the lung, despite clot formation, indicating an essential role of macrophages in this aspect [112]. Two plausible mechanisms might account for this phenomenon. In part, a recent study discovered that the recruited macrophages triggered the PI3K/Akt survival signaling pathway in newly disseminated breast cancer cells by engaging vascular cell adhesion molecule-1 (VCAM-1) via α4 integrins [113, 114]. The activation of the PI3K/Akt survival pathway subsequently saved cancer cells from proapoptotic cytokines such as TNF-related apoptosis-inducing ligand (TRAIL) [113]. In another part, many of the tumor cells survive which are protected by macrophages due to their secreted chemokines or cytokines directly secreted [112].

TAMs promote extravasation of tumor cells

Once the tumor cells settle in the capillaries of the targeted organs, they would try to attach and extrude through the vessel walls with the assistant of macrophages. The intimate contacts between tumor cells and macrophages during extravasation were visualized and quantitatively analyzed within an intact lung imaging system [115]. Of particular importance, the researchers found that the extravasation rate was dramatically declined after the loss of macrophages together with a co-incident failure of metastasis [115].

TAMs prepare sites for tumor cells: pre-metastatic niches (PMN)

It is believed that metastasis is not necessary to be a late event in tumor progression [116]. The primary tumors are smart enough to “prime” the secondary organs and dictate organ-specific dissemination before the arrival of tumor cells. Those “primed” sites are predisposed to metastasis and introduced as the concept of pre-metastatic niches (PMNs) [116]. Studies clarified that macrophages were one of the key determinants for the formation of PMNs. They were mobilized to the bloodstream and then clustered in the pre-metastatic sites by a variety of tumor-secreted factors, such as CCL2, CSF-1, VEGF, PLGF, TNF-α, TGF-β, tissue inhibitor of metallopeptidase (TIMP)-1, and exosomes [116,117,118]. Besides, the tissue-resident macrophages, such as liver Kupffer cells, pulmonary alveolar macrophages, and osteoclasts, were also involved in orchestrating PMN formation upon stimulation [119, 120]. The presence of those macrophages provide a road map for the homing of circulating tumor cells (CTCs) into the PMNs with enhanced expression of chemokines such as stromal derived factor (SDF)-1 and Ang-1 and remodel the ECM to the tumor cell-favoring direction by secreting ECM-shaping enzymes like MMPs, integrins, and lysyl oxidase (LOX), most of which have been mentioned above as critical inducers of angiogenesis, EMT, and extravasation [118,119,120,121]. Furthermore, macrophages also establish metabolic cross talk with immune cells like T helper 1 (TH1) cells and dendritic cells and attenuate their tumoricidal and tumor antigen-presenting behaviors, ultimately promoting the prosperity of those newly lodged tumor cells in a way of immunosuppression.

Potential strategies targeting macrophages

Cancer is one of the most life-threatening diseases as a major public health problem with extremely high incidence and mortality all over the world. The progression in anti-tumor research never stops. While most of the therapeutic approaches nowadays mainly focus on malignant cells themselves, only limited efficiency has been achieved. However, in-depth knowledge of the cross talk between tumor cells and TME has reoriented our approaches to strategies against pro-metastatic non-tumor components in the TME. As described above, TAMs are one of the most essential accessory cells promoting the tumor progression and metastasis by various mechanisms. More importantly, TAMs are subject to the regulation of complicated molecular signals/factors, including lots of druggable enzymes and immune checkpoint proteins. As such, therapeutic approaches targeting TAMs are anticipated to be feasible and promising. Overall, the TAM-targeted therapeutic solutions would mainly focus on strategies to eliminate TAMs, impairing macrophages infiltration and suppressing phenotype conversion of M2 from M1 [82]. Next, we will discuss the current agents based on different mechanisms including inhibiting TAMs survival, suppressing M2 polarization and inhibiting macrophages recruitment as below, and we list these related agents in Table 2.

Table 2 Clinical trials of agents targeting TAMs for cancer treatment

Agents against TAMs survival

Trabectedin is an agent with such cytotoxic efficacy to TAMs in TME; it has been approved for the treatment of patients with soft tissue sarcoma in Europe [136]. And it is also under clinical evaluation for other cancer types, including breast, prostate, and ovarian cancer [136]. Specifically, trabectedin is accepted as the cytotoxic agent directly killing tumor cells by interfering with several transcription factors, DNA-binding proteins, and DNA repair pathways [137]. Besides, its effects on the tumor microenvironment by selective mononuclear phagocyte depletion has been claimed as another key component of its antitumor activity [136]. Mechanically, trabectedin selectively induces rapid apoptosis in macrophages via TRAIL receptors and blocks their production of some pro-metastatic cytokines like CCL2, CXCL8, IL-6, and VEGF [136, 138]. The pro-apoptotic efficiency of trabectedin has been evaluated in a prospective study in which 56% (19 in 34) of soft tissue sarcoma patients experienced monocyte reduction with the extent ranging from 30~77% [136, 138]. Likewise, lurbinectedin (PM01183) is another novel anticancer agent structurally related to trabectedin. It functions by both directly killing tumor cells and affecting TAM-based immunomodulation [139]. As an analog of trabectedin, lurbinectedin exhibits potent apoptotic capacity upon macrophages, and by doing so, it dramatically decreases the number of macrophages both in circulation and TME in mice models [139]. Moreover, in the cancer cells resistant to chemotherapeutic agents, angiogenesis and distant dissemination were impaired due to lurbinectedin-caused macrophage depletion [139]. For clinical trials, various types of solid tumors in different programs are being conducted to evaluate the clinical benefits of lurbinectedin [122,123,124, 140,141,142]. However, both trabectedin and lurbinectedin cannot avoid the side effects arisen by unselectively macrophage consumption since macrophages closely participated in host defense and homeostatic regulation [140]. Thus, developing agents preferentially targeting M2-like macrophages is the “Holy Grail” to minimize potential toxic side effects. M2 macrophage-targeting peptide (M2pep), just as implied by the name, is such a construct discovered recently [143]. Researchers found that M2pep was able to exert selective toxicity to both tumor cells and M2 macrophages without influence on M1 macrophages both in vitro and in mice models [144, 145]. Based on these studies, M2pep has been turned out to be a promising adjuvant strategy for anticancer therapies, though it is still in the initial stage and needs a long way to go for substantial clinical applications.

Agents suppressing M2 polarization and enhancing M1 activity of macrophages

As described above, it is widely believed that M2 and M1 macrophages play opposite roles in tumor growth and metastasis. Therefore, proposing therapeutic strategies re-educating the pro-tumor M2 phenotype into tumoricidal M1 phenotype and thus inhibiting TAMs’ supportive roles in tumors is feasible [146]. Zoledronic acid (ZA) is an eligible agent of this kind, which has been FDA-approved as the third generation of amino-bisphosphonate agent for treating skeletal-related events (SREs) and pain caused by bone metastasis. Beyond the skeleton, plenty of studies have generated new insights into its potent role in modulating macrophages phenotypes [147]. According to those studies, ZA was able to reverse the polarity of TAMs from M2-like to M1-like by attenuating IL-10, VEGF, and MMP-9 production and recovering iNOS expression [99, 148]. Furthermore, ZA was also capable of reducing the total number of macrophages in the TME by halting TAM recruitment and infiltration [149]. Based on this evidence, zoledronic acid has been added into the adjuvant endocrine therapy for premenopausal women with early-stage breast cancer in ABCSG-12 trial [125]. Data of 62 months’ follow-up [125] showed that the addition of ZA at clinically achievable doses delayed tumor recurrence and significantly prolonged disease-free survival, which provides a solid clinical evidence for ZA to be a promising agent for cancer prevention [147, 148]. Another agent capable of repolarizing TAMs to M1 phenotype is CP-870,893, which is an agonist monoclonal antibody (mAb) of CD40 [150, 151]. CD40 belongs to the tumor necrosis factor (TNF) family and it is broadly expressed in immune cells, including macrophages. CD40-activated macrophages are indicative of M1 phenotype correlating with reinforced proinflammatory cytokines release as well as upregulated expression of antigen presentation molecules such as major histocompatibility complex (MHC)-II [152]. According to Robert H.’s study, the administration of CD40 mAb in mice was able to induce macrophage-dependent tumor regression [146]. The tolerance and activity of CP-870,893 either as a single agent or in combination with chemotherapy have been tested in several clinical trials. In the first-in-human study, a single infusion of CP-870,893 was well tolerated at the 0.2 mg/kg. Partial responses (PR) were achieved in four patients with metastatic melanoma, and one of those four patients remained in partial remission even at the 14th month [126]. What is more, in patients with advanced PDAC, CP-870,893 administration with gemcitabine was revealed to induce an objective response rate (ORR) of 19% (4 in 23 patients developed a partial response), a median progression-free survival (mPFS) of 5.6 months, and a median overall survival (OS) of 7.4 months, which are superior to the historical efficacy of single gemcitabine in PDAC (ORR of 5.4%, mPFS of 2.3 months, and mOS of 5.7 months) [127, 146]. Anyway, those clinical trials are still at an early stage with small sample size [126, 127, 146, 153]. Further randomized clinical studies with larger sample size are definitely warranted to validate their potential in clinical applications.

Agents inhibiting macrophages recruitment

As mentioned above, most of the TAMs originate from the bone marrow monocyte procurers. Recruitment of TAMs to the tumor sites or PMNs is a consequence of the continuous presence of tumor-derived chemoattractants. Therefore, cutting off those attracting signals for the macrophage recruitment appeals to be another promising solution for TAMs targeting anti-cancer therapeutic approach.

In addition to their roles in educating macrophages into M2 phenotype, both CSF-1 and CCL2 are responsible for recruiting TAMs into TME. It was reported that both small molecular inhibitors and antibodies targeting either CCL2/CCR2 or CSF-1/CSF-1R signaling axis obviously inhibited the mobilization of monocytes and macrophages accumulation in tumor sites. As a matter of fact, several inhibitors and antibodies targeting the TAM recruiting factors are being evaluated in early clinical trials across various types of tumor [132, 133, 154, 155]. For example, emactuzumab (RG7155) is a novel humanized antibody targeting CSF-1R in both ligand-dependent and ligand-independent manners [154]. Researchers found that administration of RG7155 significantly lowered the amount of CSF-1R expressing TAMs in on-treatment biopsies from tumor lesions [154]. A similar promising result has also been reported from clinical achievements in diffuse-type giant cell tumor (Dt-GCT), a neoplastic disorder characterized by CSF-1 overexpression and CSF-1R-positive TAM accumulation. In this study, among the 28 patients totally enrolled, 24 cases (86%) achieved complete response (CR) or PR, and three patients (11%) had stable disease (SD), with the average duration of response over 1.9 years [129]. However, whether this inspiring result in Dt-GCT could be carried over to other solid tumors remains a question and requires further investigation. What is more, pexidartinib (also known as PLX3397), an oral tyrosine kinase inhibitor of CSF-1R, exhibited similar efficiency (PR 52%, SD 30%, progressive disease 4%) in Dt-GCT patients as what RG7155 exhibits [130]. However, the phase II clinical trial showed no benefit from the administration of pexidartinib in 38 recurrent GBM patients [130]. But it is still worth looking forward to the results of many other ongoing clinical trials, which are conducted in c-kit-mutated melanoma, prostate cancer, sarcoma, and etc. [130]. Encouragingly, preliminary clinical benefit has been observed in a phase Ib trial evaluating the safety and effectiveness of CCX872, an orally administered CCR2 inhibitor, in patients with advanced pancreatic cancer. According to the data announced in January 2018, 29% patients receiving CCX872 and FOLFIRINOX combination therapy survived at the 18th month, more favorable than previously published OS rates of 18.6% at 18th month using FOLFIRINOX alone [132, 133]. Furthermore, a number of agents, such as CCL2 inhibitor bindarit, anti-CCL2 mAb carlumab, CSF1 inhibitor GW2580, and dequalinium-14, have been confirmed of potent and sustained anti-tumor activities via declining macrophages infiltration in a battery of cell lines and xenograft models [156,157,158,159,160]. It is conceivable that some of these agents will enter clinical trials in the near future to be further evaluated for their safety profiles and benefits in patient cohorts [155].

Conclusions and perspectives

Cancer is more of a systemic disease since metastasis occurs in the majority of patients. Effectiveness achieved by existing therapeutics is far from satisfactory, since most of the current paradigms are designed to eliminate or interdict tumor cells themselves while the successful outgrowth of metastases is largely influenced by non-malignant cells of the tumor microenvironment (TME) [5, 6, 82]. As the major orchesters of the TME, TAMs tightly regulate tumor metastasis in all of the steps involved. In this review, we discussed the implicated regulation factors participating in recruitment and polarization of TAMs. In specific, we detailedly described the underlying mechanisms for TAM-involved tumor metastasis. When we get a better understanding of the correlation between TAMs and metastasis, the potential therapeutic strategies targeting TAMs would display a promising picture for cancer intervention. Indeed, we believe that targeting the pro-metastatic components of TME and rebuilding a healthier microenvironment with a reborn capacity to hamper tumor growth will definitely hold promise for cancer therapy.

In the past decades, our mechanistic investigations of TAMs never ceased and several TAM-targeted agents are available nowadays. Although TAM-targeted therapy based on modulation of TAM survival, polarization, and recruitment is attracting more and more attention in cancer prevention and treatment, there are many fundamental hurdles lying ahead before the findings of those researches finally transmitted into clinical benefits.

Firstly, TAMs are endowed with remarkably heterogenous roles in modulating metastasis. On the one hand, while TAMs are conventionally acknowledged as M2-like, they can, in fact, exhibit phenotypes anywhere in between tumoricidal M1 type and pro-tumoral M2 type. How phenotypes switch over the course of tumor progression is not fully known. On the other hand, molecular and cell-biological details involved in promoting metastasis might be more complicated than what we expect. Various major points of regulation networks remain elusive. Therefore, it is of great necessity for us to explore the unknown mechanisms underlying TAM-facilitated metastasis and figure out more detailed TAM characterizations as well as associated molecular profiles in TME.

Secondly, in spite of inspiring preclinical data obtained from numerous laboratories, the translational benefits of agents targeting TAMs are somewhat not that satisfactory in clinical studies. No agent has received official approval for clinical use of cancer treatment so far [161, 162]. There is an intriguing possibility that tumors with different histological types and gradings, different genetic background, as well as diverse local inflammatory profiles, might have heterogenous responses to the same treatment. Therefore, there arises the tip of a far larger iceberg: what histology types or what cellular and molecular features in TME would benefit from TAM-targeted therapy? The answer is pending. Further explorations in both preclinical and clinical studies are in desperate need. In clinical practice, pathology reports do not routinely describe TAM features in tumor samples, making it difficult to identify potential TAM-target beneficiaries and creating a gap in knowledge between the clinic and tumor immunology research. Hence, figuring out TAM-related features, such as amount, phenotypes, and cytokine profiles on the pathology reports, or even assessing circulating M2 macrophage numbers as well as systemic CSF1, CCL2 levels might provide a tool for better predicting cancer metastasis and stratifying patients [158]. Furthermore, TAM-targeting therapies, either by blocking their infiltration into TME or by impairing pro-tumoral functions, are insufficient to achieve satisfying metastasis control without a direct attack on tumor cells. Approaches combining TAM-targeting agents with chemotherapeutics, irradiation, antiangiogenic agents, and immune checkpoint inhibitors may pave the way for augmented control of progression and metastasis [163, 164]. But most of these concerns have not been realized in a clinically significant way. Further studies are warranted to evaluate their therapeutic effectiveness both as a single agent or as part of a combination therapy.

When we come to talk about the immune checkpoint based therapy, it is worth noting that targeting immune checkpoint pathways, such as the innate anti-phagocytic axis of CD47-SIRPα (signal-regulatory protein alpha) pathway and LILRB receptor pathway, is emerged as one of most attractive strategy for cancer therapy. For example, CD47 expressed in tumor cells can interact with signal-regulatory protein alpha (SIRPα) which is a transmembrane protein on macrophage and the main receptor of CD47, thereby delivering the “do not eat me” signals to macrophages [165]. Studies found that the expression of CD47 increases in various tumors to evade immune attack [166]. Therefore, CD47-SIRPα interaction blockade by anti-CD47 blocking antibody increased the infiltration of macrophages in the TME, thus promoting phagocytosis of CD47+ tumor cells to exert antitumor efficacy [167, 168]. Besides, the leukocyte immunoglobulin-like receptor B (LILRB) family members are negative regulators of myeloid cell activation [169, 170]. Studies found that LILRB2 blockade by LILRB2-specific monoclonal antibodies effectively polarized macrophage cells toward an inflammatory phenotype and enhanced pro-inflammatory responses, thus acting as a myeloid immune checkpoint by reprogramming TAMs and provoking antitumor immunity [171, 172].

Thirdly, noting that TAMs do not exert functions in isolation, the TME is a complex system consists of a plethora of cells other than TAMs, such as fibroblasts, epitheliums, neutrophils, mesenchymal stem cells, myeloid cell-derived suppressor cells, and mast cells. They and their stroma around are tightly linked and interacted with each other constantly alongside the formation of metastasis [117]. Preclinical experiments targeting TAMs without the consideration of intricacy and versatility in their interactions are prone to fail in arising effective therapeutic approaches in the clinic. Hence, digging into the respective roles of those components of TME and modeling their intricate interactions evolving along with the metastasis by system biology approaches may be the avenues for future research [162].

In conclusion, this review provides an overview of our current understanding of the cross talk between TAMs and tumor cells during tumor progression, particularly in metastasis. As stated above, TAM represents a novel and attractive target that may alter the landscape of future cancer therapy, although many critical obstacles are still lying ahead and more endeavors in this aspect are needed to be done.

Availability of data and materials

Not applicable.


  1. 1.

    Seyfried TN, Huysentruyt LC. On the origin of cancer metastasis. Crit Rev Oncog. 2013;18(1-2):43–73.

    PubMed  PubMed Central  Article  Google Scholar 

  2. 2.

    Scully OJ, Bay BH, Yip G, Yu YN. Breast cancer metastasis. Cancer Genomics Proteomics. 2012;9(5):311–20.

    CAS  PubMed  PubMed Central  Google Scholar 

  3. 3.

    Fidler IJ, Kripke ML. The challenge of targeting metastasis. Cancer Metastasis Rev. 2015;34(4):635–41.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  4. 4.

    Paget S. The distribution of secondary growths in cancer of the breast. 1889. Cancer Metastasis Rev. 1989;8(2):98–101.

    CAS  PubMed  PubMed Central  Google Scholar 

  5. 5.

    Quail DF, Joyce JA. Microenvironmental regulation of tumor progression and metastasis. Nat Med. 2013;19(11):1423–37.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  6. 6.

    McAllister SS, Weinberg RA. The tumour-induced systemic environment as a critical regulator of cancer progression and metastasis. Nat Cell Biol. 2014;16(8):717–27.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  7. 7.

    Ruffell B, Affara NI, Coussens LM. Differential macrophage programming in the tumor microenvironment. Trends Immunol. 2012;33(3):119–26.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  8. 8.

    Singh S, Mehta N, Lilan J, Budhthoki MB, Chao F, Yong L. Initiative action of tumor-associated macrophage during tumor metastasis. Biochimie Open. 2017;4:8–18.

    PubMed  PubMed Central  Article  Google Scholar 

  9. 9.

    Komohara Y, Jinushi M, Takeya M. Clinical significance of macrophage heterogeneity in human malignant tumors. Cancer Sci. 2014;105(1):1–8.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  10. 10.

    Ruffell B, Coussens LM. Macrophages and therapeutic resistance in cancer. Cancer Cell. 2015;27(4):462–72.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  11. 11.

    Wynn TA, Chawla A, Pollard JW. Macrophage biology in development, homeostasis and disease. Nature. 2013;496(7446):445–55.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  12. 12.

    Lewis CE, Pollard JW. Distinct role of macrophages in different tumor microenvironments. Cancer Res. 2006;66(2):605–12.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  13. 13.

    Pollard JW. Macrophages define the invasive microenvironment in breast cancer. J Leukoc Biol. 2008;84(3):623–30.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  14. 14.

    Franklin RA, Liao W, Sarkar A, Kim MV, Bivona MR, Liu K, Pamer EG, Li MO. The cellular and molecular origin of tumor-associated macrophages. Science. 2014;344(6186):921–5.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  15. 15.

    Shand FHW, Ueha S, Otsuji M, Koid SS, Shichino S, Tsukui T, Kosugi-Kanaya M, Abe J, Tomura M, Ziogas J, Matsushima K. Tracking of intertissue migration reveals the origins of tumor-infiltrating monocytes. Proc Natl Acad Sci U S A. 2014;111(21):7771–6.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  16. 16.

    Liu Y, Cao XT. The origin and function of tumor-associated macrophages. Cell Mol Immunol. 2015;12:1.

    PubMed  Article  CAS  PubMed Central  Google Scholar 

  17. 17.

    Bain CC, Scott CL, Mowat AM. Resident and pro-inflammatory macrophages in the colon represent alternative context dependent fates of the same Ly6Chi monocyte precursors. Immunology. 2012;137:218.

    Google Scholar 

  18. 18.

    Schulz C, Perdiguero EG, Chorro L, Szabo-Rogers H, Cagnard N, Kierdorf K, Prinz M, Wu BS, Jacobsen SEW, Pollard JW, Frampton J, Liu KJ, Geissmann F. A lineage of myeloid cells independent of Myb and hematopoietic stem cells. Science. 2012;336(6077):86–90.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  19. 19.

    Sharma SK, Chintala NK, Vadrevu SK, Patel J, Karbowniczek M, Markiewski MM. Pulmonary alveolar macrophages contribute to the premetastatic niche by suppressing antitumor T cell responses in the lungs. J Immunol. 2015;194(11):5529–38.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  20. 20.

    Grivennikov SI, Wang K, Mucida D, Stewart CA, Schnabl B, Jauch D, Taniguchi K, Yu GY, Osterreicher CH, Hung KE, Datz C, Feng Y, Fearon ER, Oukka M, Tessarollo L, Coppola V, Yarovinsky F, Cheroutre H, Eckmann L, Trinchieri G, Karin M. Adenoma-linked barrier defects and microbial products drive IL-23/IL-17-mediated tumour growth. Nature. 2012;491(7423):254–8.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  21. 21.

    Kong L, Zhou Y, Bu H, Lv T, Shi Y, Yang J. Deletion of interleukin-6 in monocytes/macrophages suppresses the initiation of hepatocellular carcinoma in mice. J Exp Clin Cancer Res. 2016;35(1):131.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  22. 22.

    Laoui D, Movahedi K, Van Overmeire E, Van den Bossche J, Schouppe E, Mommer C, Nikolaou A, Morias Y, De Baetselier P, Van Ginderachter JA. Tumor-associated macrophages in breast cancer: distinct subsets, distinct functions. Int J Dev Biol. 2011;55(7-9):861–7.

    PubMed  Article  PubMed Central  Google Scholar 

  23. 23.

    Biswas SK, Mantovani A. Macrophage plasticity and interaction with lymphocyte subsets: cancer as a paradigm. Nat Immunol. 2010;11(10):889–96.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  24. 24.

    Qian BZ, Pollard JW. Macrophage diversity enhances tumor progression and metastasis. Cell. 2010;141(1):39–51.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  25. 25.

    Movahedi K, Laoui D, Gysemans C, Baeten M, Stange G, Van den Bossche J, Mack M, Pipeleers D, In't Veld P, De Baetselier P, Van Ginderachter JA. Different tumor microenvironments contain functionally distinct subsets of macrophages derived from Ly6C(high) monocytes. Cancer Res. 2010;70(14):5728–39.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  26. 26.

    Mantovani A, Sozzani S, Locati M, Allavena P, Sica A. Macrophage polarization: tumor-associated macrophages as a paradigm for polarized M2 mononuclear phagocytes. Trends Immunol. 2002;23(11):549–55.

    CAS  Article  Google Scholar 

  27. 27.

    Zhang MY, He YF, Sun XJ, Li Q, Wang WJ, Zhao AM, Di W. A high M1/M2 ratio of tumor-associated macrophages is associated with extended survival in ovarian cancer patients. J Ovarian Res. 2014;7:19.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  28. 28.

    Henze AT, Mazzone M. The impact of hypoxia on tumor-associated macrophages. J Clin Invest. 2016;126(10):3672–9.

    PubMed  PubMed Central  Article  Google Scholar 

  29. 29.

    Ohtaki Y, Ishii G, Nagai K, Ashimine S, Kuwata T, Hishida T, Nishimura M, Yoshida J, Takeyoshi I, Ochiai A. Stromal macrophage expressing CD204 is associated with tumor aggressiveness in lung adenocarcinoma. J Thorac Oncol. 2010;5(10):1507–15.

    PubMed  Article  PubMed Central  Google Scholar 

  30. 30.

    Sawa-Wejksza K, Kandefer-Szerszen M. Tumor-associated macrophages as target for antitumor therapy. Arch Immunol Ther Exp (Warsz). 2018;66(2):97–111.

    CAS  Article  Google Scholar 

  31. 31.

    Martin MD, Matrisian LM. The other side of MMPs: protective roles in tumor progression. Cancer Metastasis Rev. 2007;26(3-4):717–24.

    CAS  PubMed  Article  Google Scholar 

  32. 32.

    Kryczek I, Zou L, Rodriguez P, Zhu G, Wei S, Mottram P, Brumlik M, Cheng P, Curiel T, Myers L, Lackner A, Alvarez X, Ochoa A, Chen L, Zou W. B7-H4 expression identifies a novel suppressive macrophage population in human ovarian carcinoma. J Exp Med. 2006;203(4):871–81.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  33. 33.

    Yu H, Pardoll D, Jove R. STATs in cancer inflammation and immunity: a leading role for STAT3. Nature Rev Cancer. 2009;9(11):798–809.

    CAS  Article  Google Scholar 

  34. 34.

    Murray PJ, Wynn TA. Obstacles and opportunities for understanding macrophage polarization. J Leukoc Biol. 2011;89(4):557–63.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  35. 35.

    Heusinkveld M, van der Burg SH. Identification and manipulation of tumor associated macrophages in human cancers. J Translat Med. 2011;9:216.

    CAS  Article  Google Scholar 

  36. 36.

    Martinez FO, Gordon S, Locati M, Mantovani A. Transcriptional profiling of the human monocyte-to-macrophage differentiation and polarization: New molecules and patterns of gene expression. J Immunol. 2006;177(10):7303–11.

    CAS  PubMed  Article  Google Scholar 

  37. 37.

    Verreck FAW, de Boer T, Langenberg DML, van der Zanden L, Ottenhoff THM. Phenotypic and functional profiling of human proinflammatory type-1 and anti-inflammatory type-2 macrophages in response to microbial antigens and IFN-gamma- and CD40L-mediated costimulation. J Leukoc Biol. 2006;79(2):285–93.

    CAS  PubMed  Article  Google Scholar 

  38. 38.

    Gazzaniga S, Bravo AI, Guglielmotti A, van Rooijen N, Maschi F, Vecchi A, Mantovani A, Mordoh J, Wainstok R. Targeting tumor-associated macrophages and inhibition of MCP-1 reduce angiogenesis and tumor growth in a human melanoma xenograft. J Investig Dermatol. 2007;127(8):2031–41.

    CAS  PubMed  Article  Google Scholar 

  39. 39.

    Qian BZ, Li JF, Zhang H, Kitamura T, Zhang JH, Campion LR, Kaiser EA, Snyder LA, Pollard JW. CCL2 recruits inflammatory monocytes to facilitate breast-tumour metastasis. Nature. 2011;475(7355):222–U129.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  40. 40.

    Sierra-Filardi E, Nieto C, Dominguez-Soto A, Barroso R, Sanchez-Mateos P, Puig-Kroger A, Lopez-Bravo M, Joven J, Ardavin C, Rodriguez-Fernandez JL, Sanchez-Torres C, Mellado M, Corbi AL. CCL2 Shapes macrophage polarization by GM-CSF and M-CSF: identification of CCL2/CCR2-dependent gene expression profile. J Immunol. 2014;192(8):3858–67.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  41. 41.

    Mizutani K, Sud S, McGregor NA, Martinovski G, Rice BT, Craig MJ, Varsos ZS, Roca H, Pienta KJ. The chemokine CCL2 increases prostate tumor growth and bone metastasis through macrophage and osteoclast recruitmenT. Neoplasia. 2009;11(11):1235–42.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  42. 42.

    Abraham D, Zins K, Sioud M, Lucas T, Schafer R, Stanley ER, Aharinejad S. Stromal cell-derived CSF-1 blockade prolongs xenograft survival of CSF-1-negative neuroblastoma. Int J Cancer. 2010;126(6):1339–52.

    CAS  PubMed  PubMed Central  Google Scholar 

  43. 43.

    Hume DA, MacDonald KPA. Therapeutic applications of macrophage colony-stimulating factor-1 (CSF-1) and antagonists of CSF-1 receptor (CSF-1R) signaling. Blood. 2012;119(8):1810–20.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  44. 44.

    Ferrara N. VEGF-A: a critical regulator of blood vessel growth. Eur Cytokine Netw. 2009;20(4):158–63.

    CAS  PubMed  PubMed Central  Google Scholar 

  45. 45.

    Linde N, Lederle W, Depner S, van Rooijen N, Gutschalk CM, Mueller MM. Vascular endothelial growth factor-induced skin carcinogenesis depends on recruitment and alternative activation of macrophages. J Pathol. 2012;227(1):17–28.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  46. 46.

    Lin EY, Li J-F, Bricard G, Wang W, Deng Y, Sellers R, Porcelli SA, Pollard JW. Vascular endothelial growth factor restores delayed tumor progression in tumors depleted of macrophages. Mol Oncol. 2007;1(3):288–302.

    PubMed  PubMed Central  Article  Google Scholar 

  47. 47.

    Cursiefen C, Chen L, Borges LP, Jackson D, Cao J, Radziejewski C, D’Amore PA, Dana MR, Wiegand SJ, Streilein JW. VEGF-A stimulates lymphangiogenesis and hemangiogenesis in inflammatory neovascularization via macrophage recruitment. J Clin Invest. 2004;113(7):1040–50.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  48. 48.

    Yuxin Lin XW, Jin H. EGFR-TKI resistance in NSCLC patients: mechanisms and strategies. Am J Cancer Res. 2014;4(4):411–35.

    PubMed  PubMed Central  Google Scholar 

  49. 49.

    Lanaya H, Natarajan A, Komposch K, Li L, Amberg N, Chen L, Wculek SK, Hammer M, Zenz R, Peck-Radosavljevic M, Sieghart W, Trauner M, Wang H, Sibilia M. EGFR has a tumour-promoting role in liver macrophages during hepatocellular carcinoma formation. Nat Cell Biol. 2014;16(10):972–7.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  50. 50.

    Hardbower DM, Coburn LA, Asim M, Singh K, Sierra JC, Barry DP, Gobert AP, Piazuelo MB, Washington MK, Wilson KT. EGFR-mediated macrophage activation promotes colitis-associated tumorigenesis. Oncogene. 2017;36(27):3807–19.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  51. 51.

    Ma XY, Wu DQ, Zhou S, Wan F, Liu H, Xu XR, Xu XF, Zhao Y, Tang MC. The pancreatic cancer secreted REG4 promotes macrophage polarization to M2 through EGFR/AKT/CREB pathway. Oncol Rep. 2016;35(1):189–96.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  52. 52.

    Zhang WN, Chen LC, Ma K, Zhao YH, Liu XH, Wang Y, Liu M, Liang SF, Zhu HX, Xu NZ. Polarization of macrophages in the tumor microenvironment is influenced by EGFR signaling within colon cancer cells. Oncotarget. 2016;7(46):75366–78.

    PubMed  PubMed Central  Google Scholar 

  53. 53.

    Digiacomo G, Ziche M, Dello Sbarba P, Donnini S, Rovida E. Prostaglandin E2 transactivates the colony-stimulating factor-1 receptor and synergizes with colony-stimulating factor-1 in the induction of macrophage migration via the mitogen-activated protein kinase ERK1/2. FASEB J. 2015;29(6):2545–54.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  54. 54.

    Chen PC, Cheng HC, Wang J, Wang SW, Tai HC, Lin CW, Tang CH. Prostate cancer-derived CCN3 induces M2 macrophage infiltration and contributes to angiogenesis in prostate cancer microenvironment. Oncotarget. 2014;5(6):1595–608.

    PubMed  PubMed Central  Article  Google Scholar 

  55. 55.

    Jeannin P, Duluc D, Delneste Y. IL-6 and leukemia-inhibitory factor are involved in the generation of tumor-associated macrophage: regulation by IFN-gamma. Immunotherapy. 2011;3(4):23–6.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  56. 56.

    Noy R, Pollard JW. Tumor-associated macrophages: from mechanisms to therapy. Immunity. 2014;41(1):49–61.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  57. 57.

    Ding HX, Zhao LM, Dai SL, Li L, Wang FJ, Shan BE. CCL5 secreted by tumor associated macrophages may be a new target in treatment of gastric cancer. Biomed Pharmacother. 2016;77:142–9.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  58. 58.

    Vaupel P, Harrison L. Tumor hypoxia: causative factors, compensatory mechanisms, and cellular response. Oncologist. 2004;9:4–9.

    PubMed  Article  PubMed Central  Google Scholar 

  59. 59.

    Chae YC, Vaira V, Caino MC, Tang HY, Seo JH, Kossenkov AV, Ottobrini L, Martelli C, Lucignani G, Bertolini I, Locatelli M, Bryant KG, Ghosh JC, Lisanti S, Ku B, Bosari S, Languino LR, Speicher DW, Altieri DC. Mitochondrial Akt regulation of hypoxic tumor reprogramming. Cancer Cell. 2016;30(2):257–72.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  60. 60.

    Barsoum IB, Hamilton TK, Li X, Cotechini T, Miles EA, Siemens DR, Graham CH. Hypoxia induces escape from innate immunity in cancer cells via increased expression of ADAM10: role of nitric oxide. Cancer Res. 2011;71(24):7433–41.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  61. 61.

    Zhang CC, Sadek HA. Hypoxia and metabolic properties of hematopoietic stem cells. Antioxid Redox Signal. 2014;20(12):1891–901.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  62. 62.

    Sica A, Saccani A, Bottazzi B, Bernasconi S, Allavena P, Gaetano B, Fei P, LaRosa G, Scotton C, Balkwill F, Mantovani A. Defective expression of the monocyte chemotactic protein-1 receptor CCR2 in macrophages associated with human ovarian carcinoma. J Immunol. 2000;164(2):733–8.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  63. 63.

    Bosco MC, Reffo G, Puppo M, Varesio L. Hypoxia inhibits the expression of the CCR5 chemokine receptor in macrophages. Cell Immunol. 2004;228(1):1–7.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  64. 64.

    Chen P, Zuo H, Xiong H, Kolar MJ, Chu Q, Saghatelian A, Siegwart DJ, Wan Y. Gpr132 sensing of lactate mediates tumor-macrophage interplay to promote breast cancer metastasis. Proc Natl Acad Sci U S A. 2017;114(3):580–5.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  65. 65.

    Murdoch C, Tazzyman S, Webster S, Lewis CE. Expression of Tie-2 by human monocytes and their responses to angiopoietin-2. J Immunol. 2007;178(11):7405–11.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  66. 66.

    Venneri MA, De Palma M, Ponzoni M, Pucci F, Scielzo C, Zonari E, Mazzieri R, Doglioni C, Naldini L. Identification of proangiogenic TIE2-expressing monocytes (TEMs) in human peripheral blood and cancer. Blood. 2007;109(12):5276–85.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  67. 67.

    Laoui D, Van Overmeire E, Di Conza G, Aldeni C, Keirsse J, Morias Y, Movahedi K, Houbracken I, Schouppe E, Elkrim Y, Karroum O, Jordan B, Carmeliet P, Gysemans C, De Baetselier P, Mazzone M, Van Ginderachter JA. Tumor hypoxia does not drive differentiation of tumor-associated macrophages but rather fine-tunes the M2-like macrophage population. Cancer Res. 2014;74(1):24–30.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  68. 68.

    Sharma S, Kelly TK, Jones PA. Epigenetics in cancer. Carcinogenesis. 2010;31(1):27–36.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  69. 69.

    Dupont C, Armant DR, Brenner CA. Epigenetics: definition, mechanisms and clinical perspective. Semin Reprod Med. 2009;27(5):351–7.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  70. 70.

    Hoeksema MA, de Winther MPJ. Epigenetic regulation of monocyte and macrophage function. Antioxid Redox Signal. 2016;25(14):758–74.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  71. 71.

    Kapellos TS, Iqbal AJ. Epigenetic control of macrophage polarisation and soluble mediator gene expression during inflammation. Mediators Inflamma. 2016;2016:6591703.

    Article  CAS  Google Scholar 

  72. 72.

    Squadrito ML, Etzrodt M, De Palma M, Pittet MJ. MicroRNA-mediated control of macrophages and its implications for cancer. Trends Immunol. 2013;34(7):350–9.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  73. 73.

    Ying X, Wu QF, Wu XL, Zhu QY, Wang XJ, Jiang L, Chen X, Wang XP. Epithelial ovarian cancer-secreted exosomal miR-222-3p induces polarization of tumor-associated macrophages. Oncotarget. 2016;7(28):43076–87.

    PubMed  PubMed Central  Article  Google Scholar 

  74. 74.

    Wang Z, Xu L, Hu Y, Huang Y, Zhang Y, Zheng X, Wang S, Wang Y, Yu Y, Zhang M, Yuan K, Min W. miRNA let-7b modulates macrophage polarization and enhances tumor-associated macrophages to promote angiogenesis and mobility in prostate cancer. Sci Rep. 2016;6:25602.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  75. 75.

    Gupta GP, Massague J. Cancer metastasis: building a framework. Cell. 2006;127(4):679–95.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  76. 76.

    Savagner P. The epithelial-mesenchymal transition (EMT) phenomenon. Ann Oncol. 2010;21(Suppl 7):vii89–92.

    PubMed  PubMed Central  Google Scholar 

  77. 77.

    Lamouille S, Xu J, Derynck R. Molecular mechanisms of epithelial-mesenchymal transition. Nat Rev Mol Cell Biol. 2014;15(3):178–96.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  78. 78.

    Moustakas A, Heldin CH. Signaling networks guiding epithelial-mesenchymal transitions during embryogenesis and cancer progression. Cancer Sci. 2007;98(10):1512–20.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  79. 79.

    Su SC, Liu Q, Chen JQ, Chen JN, Chen F, He CH, Huang D, Wu W, Lin L, Huang W, Zhang J, Cui XY, Zheng F, Li HY, Yao HR, Su FX, Song EW. A positive feedback loop between Mesenchymal-like cancer cells and macrophages is essential to breast cancer metastasis. Cancer Cell. 2014;25(5):605–20.

    PubMed  Article  CAS  PubMed Central  Google Scholar 

  80. 80.

    Fu XT, Dai Z, Song K, Zhang ZJ, Zhou ZJ, Zhou SL, Zhao YM, Xiao YS, Sun QM, Ding ZB, Fan J. Macrophage-secreted IL-8 induces-epithelial-mesenchymal transition in hepatocellular carcinoma cells by activating the JAK2/STAT3/Snail pathway. Int J Oncol. 2015;46(2):587–96.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  81. 81.

    Ravi J, Elbaz M, Wani NA, Nasser MW, Ganju RK. Cannabinoid receptor-2 agonist inhibits macrophage induced EMT in non-small cell lung cancer by downregulation of EGFR pathway. Mol Carcinog. 2016;55(12):2063–76.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  82. 82.

    Helm O, Held-Feindt J, Grage-Griebenow E, Reiling N, Ungefroren H, Vogel I, Kruger U, Becker T, Ebsen M, Rocken C, Kabelitz D, Schafer H, Sebens S. Tumor-associated macrophages exhibit pro- and anti-inflammatory properties by which they impact on pancreatic tumorigenesis. Int J Cancer. 2014;135(4):843–61.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  83. 83.

    Wu Y, Deng J, Rychahou PG, Qiu SM, Evers BM, Zhou BPH. Stabilization of Snail by NF-kappa B Is required for inflammation-induced cell migration and invasion. Cancer Cell. 2009;15(5):416–28.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  84. 84.

    Kawata M, Koinuma D, Ogami T, Umezawa K, Iwata C, Watabe T, Miyazono K. TGF-beta-induced epithelial-mesenchymal transition of A549 lung adenocarcinoma cells is enhanced by pro-inflammatory cytokines derived from RAW 264.7 macrophage cells. J Biochem. 2012;151(2):205–16.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  85. 85.

    Chambers DBJGA. Extracellular matrix: a gatekeeper in the transition from dormancy to metastatic growth. Eur J Cancer. 2010;46(7):1181–8.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  86. 86.

    Kessenbrock K, Plaks V, Werb Z. Matrix metalloproteinases: regulators of the tumor microenvironment. Cell. 2010;141(1):52–67.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  87. 87.

    Vasiljeva O, Papazoglou A, Kruger A, Brodoefel H, Korovin M, Deussing J, Augustin N, Nielsen BS, Almholt K, Bogyo M, Peters C, Reinheckel T. Tumor cell-derived and macrophage-derived cathepsin B promotes progression and lung metastasis of mammary cancer. Cancer Res. 2006;66(10):5242–50.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  88. 88.

    Gocheva V, Wang HW, Gadea BB, Shree T, Hunter KE, Garfall AL, Berman T, Joyce JA. IL-4 induces cathepsin protease activity in tumor-associated macrophages to promote cancer growth and invasion. Genes Dev. 2010;24(3):241–55.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  89. 89.

    Chen Y, Zhang S, Wang Q, Zhang X. Tumor-recruited M2 macrophages promote gastric and breast cancer metastasis via M2 macrophage-secreted CHI3L1 protein. J Hematol Oncol. 2017;10(1):36.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  90. 90.

    Sangaletti S, Di Carlo E, Gariboldi S, Miotti S, Cappetti B, Parenza M, Rumio C, Brekken RA, Chiodoni C, Colombo MP. Macrophage-derived SPARC bridges tumor cell-extracellular matrix interactions toward metastasis. Cancer Res. 2008;68(21):9050–9.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  91. 91.

    Condeelis J, Segall JE. Intravital imaging of cell movement in tumours. Nat Rev Cancer. 2003;3(12):921–30.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  92. 92.

    Barker TH, Baneyx G, Cardo-Vila M, Workman GA, Weaver M, Menon PM, Dedhar S, Rempel SA, Arap W, Pasqualini R, Vogel V, Sage EH. SPARC regulates extracellular matrix organization through its modulation of integrin-linked kinase activity. J Biol Chem. 2005;280(43):36483–93.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  93. 93.

    Brekken RA, Puolakkainen P, Graves DC, Workman G, Lubkin SR, Sage EH. Enhanced growth of tumors in SPARC null mice is associated with changes in the ECM. J Clin Invest. 2003;111(4):487–95.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  94. 94.

    Hanahan D, Christofori G, Naik P, Arbeit J. Transgenic mouse models of tumour angiogenesis: The angiogenic switch, its molecular controls, and prospects for preclinical therapeutic models. Eur J Cancer. 1996;32a(14):2386–93.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  95. 95.

    Metcalf S, Pandha HS, Morgan R. Antiangiogenic effects of zoledronate on cancer neovasculature. Future Oncol. 2011;7(11):1325–33.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  96. 96.

    Lin EY, Li JF, Gnatovskiy L, Deng Y, Zhu L, Grzesik DA, Qian H, Xue XN, Pollard JW. Macrophages regulate the angiogenic switch in a mouse model of breast cancer. Cancer Res. 2006;66(23):11238–46.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  97. 97.

    Lin EY, Pollard JW. Tumor-associated macrophages press the angiogenic switch in breast cancer. Cancer Res. 2007;67(11):5064–6.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  98. 98.

    Bergers G, Brekken R, McMahon G, Vu TH, Itoh T, Tamaki K, Tanzawa K, Thorpe P, Itohara S, Werb Z, Hanahan D. Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis. Nat Cell Biol. 2000;2(10):737–44.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  99. 99.

    Giraudo E, Inoue M, Hanahan D. An amino-bisphosphonate targets MMP-9-expressing macrophages and angiogenesis to impair cervical carcinogenesis. J Clin Invest. 2004;114(5):623–33.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  100. 100.

    Matsubara T, Kanto T, Kuroda S, Yoshio S, Higashitani K, Kakita N, Miyazaki M, Sakakibara M, Hiramatsu N, Kasahara A, Tomimaru Y, Tomokuni A, Nagano H, Hayashi N, Takehara T. TIE2-expressing monocytes as a diagnostic marker for hepatocellular carcinoma correlates with angiogenesis. Hepatology. 2013;57(4):1416–25.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  101. 101.

    Riabov V, Gudima A, Wang N, Mickley A, Orekhov A, Kzhyshkowska J. Role of tumor associated macrophages in tumor angiogenesis and lymphangiogenesis. Front Physiol. 2014;5:75.

    PubMed  PubMed Central  Article  Google Scholar 

  102. 102.

    Cao RH, Ji H, Yang YL, Cao YH. Collaborative effects between the TNF alpha-TNFR1-macrophage axis and the VEGF-C-VEGFR3 signaling in lymphangiogenesis and metastasis. Oncoimmunology. 2015;4:3.

    Article  CAS  Google Scholar 

  103. 103.

    Alishekevitz D, Gingis-Velitski S, Kaidar-Person O, Gutter-Kapon L, Scherer SD, Raviv Z, Merquiol E, Ben-Nun Y, Miller V, Rachman-Tzemah C, Timaner M, Mumblat Y, Ilan N, Loven D, Hershkovitz D, Satchi-Fainaro R, Blum G, Sleeman JP, Vlodavsky I, Shaked Y. Macrophage-induced lymphangiogenesis and metastasis following paclitaxel chemotherapy is regulated by VEGFR3. Cell Rep. 2016;17(5):1344–56.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  104. 104.

    Wyckoff JB, Jones JG, Condeelis JS, Segall JE. A critical step in metastasis: in vivo analysis of intravasation at the primary tumor. Cancer Res. 2000;60(9):2504–11.

    CAS  PubMed  PubMed Central  Google Scholar 

  105. 105.

    Wyckoff JB, Wang Y, Lin EY, Li JF, Goswami S, Stanley ER, Segall JE, Pollard JW, Condeelis J. Direct visualization of macrophage-assisted tumor cell intravasation in mammary tumors. Cancer Res. 2007;67(6):2649–56.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  106. 106.

    Wang J, Cao Z, Zhang XM, Nakamura M, Sun M, Hartman J, Harris RA, Sun Y, Cao Y. Novel mechanism of macrophage-mediated metastasis revealed in a zebrafish model of tumor development. Cancer Res. 2015;75(2):306–15.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  107. 107.

    Robinson BD, Sica GL, Liu YF, Rohan TE, Gertler FB, Condeelis JS, Jones JG. Tumor microenvironment of metastasis in human breast carcinoma: a potential prognostic marker linked to hematogenous dissemination. Clin Cancer Res. 2009;15(7):2433–41.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  108. 108.

    Wyckoff J, Wang WG, Lin EY, Wang YR, Pixley F, Stanley ER, Graf T, Pollard JW, Segall J, Condeelis J. A paracrine loop between tumor cells and macrophages is required for tumor cell migration in mammary tumors. Cancer Res. 2004;64(19):7022–9.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  109. 109.

    Goswami S, Sahai E, Wyckoff JB, Cammer N, Cox D, Pixley FJ, Stanley ER, Segall JE, Condeelis JS. Macrophages promote the invasion of breast carcinoma cells via a colony-stimulating factor-1/epidermal growth factor paracrine loop. Cancer Res. 2005;65(12):5278–83.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  110. 110.

    Nierodzik ML, Karpatkin S. Thrombin induces tumor growth, metastasis, and angiogenesis: Evidence for a thrombin-regulated dormant tumor phenotype. Cancer Cell. 2006;10(5):355–62.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  111. 111.

    Palumbo JS, Talmage KE, Massari JV, La Jeunesse CM, Flick MJ, Kombrinck KW, Hu Z, Barney KA, Degen JL. Tumor cell-associated tissue factor and circulating hemostatic factors cooperate to increase metastatic potential through natural killer cell-dependent and-independent mechanisms. Blood. 2007;110(1):133–41.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  112. 112.

    Gil-Bernabe AM, Ferjancic S, Tlalka M, Zhao L, Allen PD, Im JH, Watson K, Hill SA, Amirkhosravi A, Francis JL, Pollard JW, Ruf W, Muschel RJ. Recruitment of monocytes/macrophages by tissue factor-mediated coagulation is essential for metastatic cell survival and premetastatic niche establishment in mice. Blood. 2012;119(13):3164–75.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  113. 113.

    Chen Q, Zhang XH, Massague J. Macrophage binding to receptor VCAM-1 transmits survival signals in breast cancer cells that invade the lungs. Cancer Cell. 2011;20(4):538–49.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  114. 114.

    Lu X, Mu E, Wei Y, Riethdorf S, Yang Q, Yuan M, Yan J, Hua Y, Tiede BJ, Lu X, Haffty BG, Pantel K, Massague J, Kang Y. VCAM-1 promotes osteolytic expansion of indolent bone micrometastasis of breast cancer by engaging alpha4beta1-positive osteoclast progenitors. Cancer Cell. 2011;20(6):701–14.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  115. 115.

    Qian B, Deng Y, Im JH, Muschel RJ, Zou Y, Li J, Lang RA, Pollard JW. A distinct macrophage population mediates metastatic breast cancer cell extravasation, establishment and growth. PLoS One. 2009;4(8):e6562.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  116. 116.

    Kaplan RN, Riba RD, Zacharoulis S, Bramley AH, Vincent L, Costa C, MacDonald DD, Jin DK, Shido K, Kerns SA, Zhu ZP, Hicklin D, Wu Y, Port JL, Altorki N, Port ER, Ruggero D, Shmelkov SV, Jensen KK, Rafii S, Lyden D. VEGFR1-positive haematopoietic bone marrow progenitors initiate the pre-metastatic niche. Nature. 2005;438(7069):820–7.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  117. 117.

    Joyce JA, Pollard JW. Microenvironmental regulation of metastasis. Nat Rev Cancer. 2009;9(4):239–52.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  118. 118.

    Sceneay J, Smyth MJ, Moller A. The pre-metastatic niche: finding common ground. Cancer Metastasis Rev. 2013;32(3-4):449–64.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  119. 119.

    Kaplan RN, Psaila B, Lyden D. Bone marrow cells in the ‘pre-metastatic niche’: within bone and beyond. Cancer Metastasis Rev. 2006;25(4):521–9.

    PubMed  Article  PubMed Central  Google Scholar 

  120. 120.

    Lu X, Kang YB. Organotropism of breast cancer metastasis. J Mammary Gland Biol Neoplasia. 2007;12(2-3):153–62.

    PubMed  Article  PubMed Central  Google Scholar 

  121. 121.

    Muller A, Homey B, Soto H, Ge NF, Catron D, Buchanan ME, McClanahan T, Murphy E, Yuan W, Wagner SN, Barrera JL, Mohar A, Verastegui E, Zlotnik A. Involvement of chemokine receptors in breast cancer metastasis. Nature. 2001;410(6824):50–6.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  122. 122.

    Elez ME, Tabernero J, Geary D, Macarulla T, Kang SP, Kahatt C, Pita ASM, Teruel CF, Siguero M, Cullell-Young M, Szyldergemajn S, Ratain MJ. First-in-human phase I study of lurbinectedin (PM01183) in patients with advanced solid tumors. Clin Cancer Res. 2014;20(8):2205–14.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  123. 123.

    Poveda A, del Campo JM, Ray-Coquard I, Alexandre J, Provansal M, Alia EMG, Casado A, Gonzalez-Martin A, Fernandez C, Rodriguez I, Soto A, Kahatt C, Teruel CF, Galmarini CM, de la Haza AP, Bohan P, Berton-Rigaud D. Phase II randomized study of PM01183 versus topotecan in patients with platinum-resistant/refractory advanced ovarian cancer. Ann Oncol. 2017;28(6):1280–7.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  124. 124.

    Paz-Ares L, Forster M, Boni V, Szyldergemajn S, Corral J, Turnbull S, Cubillo A, Teruel CF, Calderero IL, Siguero M, Bohan P, Calvo E. Phase I clinical and pharmacokinetic study of PM01183 (a tetrahydroisoquinoline, Lurbinectedin) in combination with gemcitabine in patients with advanced solid tumors. Invest New Drugs. 2017;35(2):198–206.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  125. 125.

    Gnant M, Mlineritsch B, Stoeger H, Luschin-Ebengreuth G, Heck D, Menzel C, Jakesz R, Seifert M, Hubalek M, Pristauz G, Bauernhofer T, Eidtmann H, Eiermann W, Steger G, Kwasny W, Dubsky P, Hochreiner G, Forsthuber EP, Fesl C, Greil R, Austrian B, Colorectal Cancer Study Group VA. Adjuvant endocrine therapy plus zoledronic acid in premenopausal women with early-stage breast cancer: 62-month follow-up from the ABCSG-12 randomised trial. Lancet Oncol. 2011;12(7):631–41.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  126. 126.

    Vonderheide RH, Flaherty KT, Khalil M, Stumacher MS, Bajor DL, Hutnick NA, Sullivan P, Mahany JJ, Gallagher M, Kramer A, Green SJ, O'Dwyer PJ, Running KL, Huhn RD, Antonia SJ. Clinical activity and immune modulation in cancer patients treated with CP-870,893, a novel CD40 agonist monoclonal antibody. J Clin Oncol. 2007;25(7):876–83.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  127. 127.

    Beatty GL, Torigian DA, Chiorean EG, Saboury B, Brothers A, Alavi A, Troxel AB, Sun W, Teitelbaum UR, Vonderheide RH, O'Dwyer PJ. A phase I study of an agonist CD40 monoclonal antibody (CP-870,893) in combination with gemcitabine in patients with advanced pancreatic ductal adenocarcinoma. Clin Cancer Res. 2013;19(22):6286–95.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  128. 128.

    Gomez-Roca CA, Cassier PA, Italiano A, Cannarile M, Ries C, Brillouet A, Mueller C, Jegg AM, Meneses-Lorente G, Baehner M, Abiraj K, Loirat D, Toulmonde M, D'Angelo SP, Weber K, Campone M, Ruettinger D, Blay JY, Delord JP, Le Tourneau C. Phase I study of RG7155, a novel anti-CSF1R antibody, in patients with advanced/metastatic solid tumors. J Clin Oncol. 2015;33:15.

    Article  Google Scholar 

  129. 129.

    Ries CH, Cannarile MA, Hoves S, Benz J, Wartha K, Runza V, Rey-Giraud F, Pradel LP, Feuerhake F, Klaman I, Jones T, Jucknischke U, Scheiblich S, Kaluza K, Gorr IH, Walz A, Abiraj K, Cassier PA, Sica A, Gomez-Roca C, de Visser KE, Italiano A, Le Tourneau C, Delord JP, Levitsky H, Blay JY, Ruttinger D. Targeting tumor-associated macrophages with anti-CSF-1R antibody reveals a strategy for cancer therapy. Cancer Cell. 2014;25(6):846–59.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  130. 130.

    Butowski N, Colman H, De Groot JF, Omuro AM, Nayak L, Wen PY, Cloughesy TF, Marimuthu A, Haidar S, Perry A, Huse J, Phillips J, West BL, Nolop KB, Hsu HH, Ligon KL, Molinaro AM, Prados M. Orally administered colony stimulating factor 1 receptor inhibitor PLX3397 in recurrent glioblastoma: an Ivy Foundation Early Phase Clinical Trials Consortium phase II study. Neuro Oncol. 2016;18(4):557–64.

    PubMed  Article  PubMed Central  Google Scholar 

  131. 131.

    Bendell JC, Tolcher AW, Jones SF, Beeram M, Infante JR, Larsen P, Rasor K, Garrus JE, Li JF, Cable PL, Eberhardt C, Schreiber J, Rush S, Wood KW, Barret E, Patnaik A. A phase 1 study of ARRY-382, an oral inhibitor of colony-stimulating factor-1 receptor (CSF1R), in patients with advanced or metastatic cancers. Mol Cancer Ther. 2013;12:11.

    Article  CAS  Google Scholar 

  132. 132.

    Noel MS, Hezel AF, Linehan D, Wang-Gillam A, Eskens F, Sleijfer S, Desar I, Erdkamp F, Wilmink J, Diehl J, Potarca A, Zhao N, Deng J, Lohr L, Miao SC, Charo I, Singh R, Schall TJ, Bekker P. Orally administered CCR2 selective inhibitor CCX872-b clinical trial in pancreatic cancer. J Clin Oncol. 2017;35:4.

    Article  Google Scholar 

  133. 133.

    Linehan D, Noel MS, Hezel AF, Wang-Gillam A, Eskens F, Sleijfer S, Desar IM, Erdkamp F, Wilmink J, Diehl J, Potarca A, Zhao N, Miao S, Deng J, Hillson J, Bekker P, Schall TJ, Singh R. Overall survival in a trial of orally administered CCR2 inhibitor CCX872 in locally advanced/metastatic pancreatic cancer: Correlation with blood monocyte counts. J Clin Oncol. 2018;36:5.

    Article  Google Scholar 

  134. 134.

    Nywening TM, Wang-Gillam A, Sanford DE, Belt BA, Panni RZ, Cusworth BM, Toriola AT, Nieman RK, Worley LA, Yano M, Fowler KJ, Lockhart AC, Suresh R, Tan BR, Lim KH, Fields RC, Strasberg SM, Hawkins WG, DG DN, Goedegebuure SP, Linehan DC. Targeting tumour-associated macrophages with CCR2 inhibition in combination with FOLFIRINOX in patients with borderline resectable and locally advanced pancreatic cancer: a single-centre, open-label, dose-finding, non-randomised, phase 1b trial. Lancet Oncol. 2016;17(5):651–62.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  135. 135.

    Yang L, Zhang Y. Tumor-associated macrophages: from basic research to clinical application. J Hematol Oncol. 2017;10(1):58.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  136. 136.

    Germano G, Frapolli R, Belgiovine C, Anselmo A, Pesce S, Liguori M, Erba E, Uboldi S, Zucchetti M, Pasqualini F, Nebuloni M, van Rooijen N, Mortarini R, Beltrame L, Marchini S, Fuso Nerini I, Sanfilippo R, Casali PG, Pilotti S, Galmarini CM, Anichini A, Mantovani A, D'Incalci M, Allavena P. Role of macrophage targeting in the antitumor activity of trabectedin. Cancer Cell. 2013;23(2):249–62.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  137. 137.

    D'Incalci M, Galmarini CM. A review of trabectedin (ET-743): a unique mechanism of action. Mol Cancer Ther. 2010;9(8):2157–63.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  138. 138.

    D'Incalci M. Trabectedin mechanism of action: what’s new? Future Oncol. 2013;9(12):5–10.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  139. 139.

    Belgiovine C, Bello E, Liguori M, Craparotta I, Mannarino L, Paracchini L, Beltrame L, Marchini S, Galmarini CM, Mantovani A, Frapolli R, Allavena P, D’Incalci M. Lurbinectedin reduces tumour-associated macrophages and the inflammatory tumour microenvironment in preclinical models. Br J Cancer. 2017;117(5):628–38.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  140. 140.

    Gordon S, Taylor PR. Monocyte and macrophage heterogeneity. Nat Rev Immunol. 2005;5(12):953–64.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  141. 141.

    Cespedes MV, Guillen MJ, Lopez-Casas PP, Sarno F, Gallardo A, Alamo P, Cuevas C, Hidalgo M, Galmarini CM, Allavena P, Aviles P, Mangues R. Lurbinectedin induces depletion of tumor-associated macrophages, an essential component of its in vivo synergism with gemcitabine, in pancreatic adenocarcinoma mouse models. Dis Model Mech. 2016;9(12):1461–71.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  142. 142.

    Calvo E, Moreno V, Flynn M, Holgado E, Olmedo ME, Criado MPL, Kahatt C, Lopez-Vilarino JA, Siguero M, Fernandez-Teruel C, Cullell-Young M, Matos-Pita AS, Forster M. Antitumor activity of lurbinectedin (PM01183) and doxorubicin in relapsed small-cell lung cancer: results from a phase I study. Ann Oncol. 2017;28(10):2559–66.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  143. 143.

    Cieslewicz M, Tang J, Yu JL, Cao H, Zavaljevski M, Motoyama K, Lieber A, Raines EW, Pun SH. Targeted delivery of proapoptotic peptides to tumor-associated macrophages improves survival. Proc Natl Acad Sci U S A. 2013;110(40):15919–24.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  144. 144.

    Ngambenjawong C, Cieslewicz M, Schellinger JG, Pun SH. Synthesis and evaluation of multivalent M2pep peptides for targeting alternatively activated M2 macrophages. J Control Release. 2016;224:103–11.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  145. 145.

    Kakoschky B, Pleli T, Schmithals C, Zeuzem S, Brune B, Vogl TJ, Korf HW, Weigert A, Piiper A. Selective targeting of tumor associated macrophages in different tumor models. PLoS One. 2018;13(2):e0193015.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  146. 146.

    Beatty GL, Chiorean EG, Fishman MP, Saboury B, Teitelbaum UR, Sun W, Huhn RD, Song W, Li D, Sharp LL, Torigian DA, O’Dwyer PJ, Vonderheide RH. CD40 agonists alter tumor stroma and show efficacy against pancreatic carcinoma in mice and humans. Science. 2011;331(6024):1612–6.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  147. 147.

    Comito G, Segura CP, Sobierajska K, Ippolito L, Taddei ML, Giannoni E, Chiarugi P. Zoledronic acid impairs stromal reactivity by inhibiting M2-macrophages polarization and prostate cancer-associated fibroblasts. Eur J Cancer. 2014;50:S74.

    Article  Google Scholar 

  148. 148.

    Coscia M, Quaglino E, Iezzi M, Curcio C, Pantaleoni F, Riganti C, Holen I, Monkkonen H, Boccadoro M, Forni G, Musiani P, Bosia A, Cavallo F, Massaia M. Zoledronic acid repolarizes tumour-associated macrophages and inhibits mammary carcinogenesis by targeting the mevalonate pathway. J Cell Mol Med. 2010;14(12):2803–15.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  149. 149.

    Rogers TL, Wind N, Hughes R, Nutter F, Brown HK, Vasiliadou I, Ottewell PD, Holen I. Macrophages as potential targets for zoledronic acid outside the skeleton-evidence from in vitro and in vivo models. Cell Oncol (Dordr). 2013;36(6):505–14.

    CAS  Article  Google Scholar 

  150. 150.

    Vonderheide RH, Bajor DL, Winograd R, Evans RA, Bayne LJ, Beatty GL. CD40 immunotherapy for pancreatic cancer. Cancer Immunol Immunother. 2013;62(5):949–54.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  151. 151.

    Vonderheide RH. Prospect of targeting the CD40 pathway for cancer therapy. Clin Cancer Res. 2007;13(4):1083–8.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  152. 152.

    Suttles J, Stout RD. Macrophage CD40 signaling: a pivotal regulator of disease protection and pathogenesis. Semin Immunol. 2009;21(5):257–64.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  153. 153.

    Nowak AK, Cook AM, McDonnell AM, Millward MJ, Creaney J, Francis RJ, Hasani A, Segal A, Musk AW, Turlach BA, McCoy MJ, Robinson BW, Lake RA. A phase 1b clinical trial of the CD40-activating antibody CP-870,893 in combination with cisplatin and pemetrexed in malignant pleural mesothelioma. Ann Oncol. 2015;26(12):2483–90.

    CAS  PubMed  PubMed Central  Google Scholar 

  154. 154.

    Pradel LP, Ooi CH, Romagnoli S, Cannarile MA, Sade H, Ruttinger D, Ries CH. Macrophage susceptibility to emactuzumab (RG7155) treatment. Mol Cancer Ther. 2016;15(12):3077–86.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  155. 155.

    Cannarile MA, Weisser M, Jacob W, Jegg AM, Ries CH, Ruttinger D. Colony-stimulating factor 1 receptor (CSF1R) inhibitors in cancer therapy. J Immunother Cancer. 2017;5:53.

    PubMed  PubMed Central  Article  Google Scholar 

  156. 156.

    Priceman SJ, Sung JL, Shaposhnik Z, Burton JB, Torres-Collado AX, Moughon DL, Johnson M, Lusis AJ, Cohen DA, Iruela-Arispe ML, Wu L. Targeting distinct tumor-infiltrating myeloid cells by inhibiting CSF-1 receptor: combating tumor evasion of antiangiogenic therapy. Blood. 2010;115(7):1461–71.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  157. 157.

    Steiner JL, Davis JM, McClellan JL, Guglielmotti A, Murphy EA. Effects of the MCP-1 synthesis inhibitor bindarit on tumorigenesis and inflammatory markers in the C3(1)/SV40Tag mouse model of breast cancer. Cytokine. 2014;66(1):60–8.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  158. 158.

    Swierczak A, Cook AD, Lenzo JC, Restall CM, Doherty JP, Anderson RL, Hamilton JA. The promotion of breast cancer metastasis caused by inhibition of CSF-1R/CSF-1 signaling is blocked by targeting the G-CSF receptor. Cancer Immunol Res. 2014;2(8):765–76.

    CAS  PubMed  Article  Google Scholar 

  159. 159.

    Moughon DL, He HH, Schokrpur S, Jiang ZK, Yaqoob M, David J, Lin C, Iruela-Arispe ML, Dorigo O, Wu L. Macrophage blockade using CSF1R inhibitors reverses the vascular leakage underlying malignant ascites in late-stage epithelial ovarian cancer. Cancer Res. 2015;75(22):4742–52.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  160. 160.

    Timaner M, Bril R, Kaidar-Person O, Rachman-Tzemah C, Alishekevitz D, Kotsofruk R, Miller V, Nevelsky A, Daniel S, Raviv Z, Rotenberg SA, Shaked Y. Dequalinium blocks macrophage-induced metastasis following local radiation. Oncotarget. 2015;6(29):27537–54.

    PubMed  PubMed Central  Article  Google Scholar 

  161. 161.

    Keklikoglou I, De Palma M. Cancer: metastasis risk after anti-macrophage therapy. Nature. 2014;515(7525):46–7.

    CAS  PubMed  Article  Google Scholar 

  162. 162.

    Bonapace L, Coissieux MM, Wyckoff J, Mertz KD, Varga Z, Junt T, Bentires-Alj M. Cessation of CCL2 inhibition accelerates breast cancer metastasis by promoting angiogenesis. Nature. 2014;515(7525):130–3.

    CAS  PubMed  Article  Google Scholar 

  163. 163.

    Torres-Collado SPJSZSJBA. Targeting distinct tumor-infiltrating myeloid cells by inhibiting CSF-1 receptor: combating tumor evasion of antiangiogenic therapy. Blood. 2010;115(7):1461.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  164. 164.

    Xu J, Escamilla J, Mok S, David J, Priceman S, West B, Bollag G, McBride W, Wu L. CSF1R signaling blockade stanches tumor-infiltrating myeloid cells and improves the efficacy of radiotherapy in prostate cancer. Cancer Res. 2013;73(9):2782–94.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  165. 165.

    Weiskopf K. Cancer immunotherapy targeting the CD47/SIRP alpha axis. Eur J Cancer. 2017;76:100–9.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  166. 166.

    Liu XJ, Kwon H, Li ZH, Fu YX. Is CD47 an innate immune checkpoint for tumor evasion? J Hematol Oncol. 2017;10:12.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  167. 167.

    Gu SL, Ni T, Wang J, Liu Y, Fan Q, Wang YW, Huang T, Chu YW, Sun X, Wang YD. CD47 blockade inhibits tumor progression through promoting phagocytosis of tumor cells by M2 polarized macrophages in endometrial cancer. J Immunol Res. 2018;2018:6156757.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  168. 168.

    Alvey C, Discher DE. Engineering macrophages to eat cancer: from “marker of self” CD47 and phagocytosis to differentiation. J Leukoc Biol. 2017;102(1):31–40.

    CAS  PubMed  Article  PubMed Central  Google Scholar 

  169. 169.

    Ma G, Pan PY, Eisenstein S, Divino CM, Lowell CA, Takai T, Chen SH. Paired immunoglobin-like receptor-B regulates the suppressive function and fate of myeloid-derived suppressor cells. Immunity. 2011;34(3):385–95.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  170. 170.

    van der Touw W, Chen HM, Pan PY, Chen SH. LILRB receptor-mediated regulation of myeloid cell maturation and function. Cancer Immunol Immunother. 2017;66(8):1079–87.

    PubMed  PubMed Central  Article  CAS  Google Scholar 

  171. 171.

    Zhang J, Mai S, Chen HM, Kang K, Li XC, Chen SH, Pan PY. Leukocyte immunoglobulin-like receptors in human diseases: an overview of their distribution, function, and potential application for immunotherapies. J Leukoc Biol. 2017;102(2):351–60.

    CAS  PubMed  PubMed Central  Article  Google Scholar 

  172. 172.

    Chen HM, van der Touw W, Wang YS, Kang K, Mai S, Zhang JL, Alsina-Beauchamp D, Duty JA, Mungamuri SK, Zhang B, Moran T, Flavell R, Aaronson S, Hu HM, Arase H, Ramanathan S, Flores R, Pan PY, Chen SH. Blocking immunoinhibitory receptor LILRB2 reprograms tumor-associated myeloid cells and promotes antitumor immunity. J Clin Invest. 2018;128(12):5647–62.

    PubMed  PubMed Central  Article  Google Scholar 

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This work was supported by the Key Chinese Traditional Medicine Specialty Project of Huzhou City (2016ZZ07).

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YXL was involved in the drafting of the manuscript. HYL was involved in the editing and revising of the manuscript critically for the important scientific content. JXX was involved in the editing of the content and providing the final approval of the version to be published. All authors read and approved the final manuscript.

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Correspondence to Jianxin Xu or Huiyin Lan.

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Lin, Y., Xu, J. & Lan, H. Tumor-associated macrophages in tumor metastasis: biological roles and clinical therapeutic applications. J Hematol Oncol 12, 76 (2019).

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  • Metastasis
  • Macrophages
  • TAMs
  • TME
  • Polarization