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Targeting cuproptosis for cancer therapy: mechanistic insights and clinical perspectives
Journal of Hematology & Oncology volume 17, Article number: 68 (2024)
Abstract
Cuproptosis is a newly identified form of cell death induced by excessive copper (Cu) accumulation within cells. Mechanistically, cuproptosis results from Cu-induced aggregation of dihydrolipoamide S-acetyltransferase, correlated with the mitochondrial tricarboxylic acid cycle and the loss of iron–sulfur cluster proteins, ultimately resulting in proteotoxic stress and triggering cell death. Recently, cuproptosis has garnered significant interest in tumor research due to its potential as a crucial therapeutic strategy against cancer. In this review, we summarized the cellular and molecular mechanisms of cuproptosis and its relationship with other types of cell death. Additionally, we reviewed the current drugs or strategies available to induce cuproptosis in tumor cells, including Cu ionophores, small compounds, and nanomedicine. Furthermore, we targeted cell metabolism and specific regulatory genes in cancer therapy to enhance tumor sensitivity to cuproptosis. Finally, we discussed the feasibility of targeting cuproptosis to overcome tumor chemotherapy and immunotherapy resistance and suggested future research directions. This study suggested that targeting cuproptosis could open new avenues for developing tumor therapy.
Introduction
Copper (Cu) is an essential trace metal element for normal physiological functions primarily obtained from dietary supplements. In biological systems, Cu exists predominantly in two oxidative states: divalent copper ions (Cu2+) and monovalent copper ions (Cu+). Cu+ is the principal oxidative form and plays a significant role in physiological and pathological regulation within cells [1,2,3]. Disruptions in Cu homeostasis can induce disease onset; for instance, Cu overload may lead to Wilson’s disease [4], while Cu deficiency can cause Menkes disease [5]. Furthermore, previous studies have demonstrated that Cu could promote tumor cell proliferation, angiogenesis, and metastasis and reduces the efficacy of tumor treatments [6].
However, excess Cu in the cells can also cause cellular damage. Researchers observed that using Cu ionophores to elevate Cu levels within tumor cells could cause cell death [7, 8]. Although subsequent studies have extensively investigated the molecular mechanisms underlying Cu-induced cell death, such as the association of this type of cell death with reactive oxygen species (ROS), apoptosis, and ferroptosis-related signaling pathways, the key mechanisms remain unclear. Tsvetkov et al. termed the Cu-induced cell death cuproptosis in 2022 based on their findings that this form of cell death depends on the aggregation of lipoylated dihydrolipoamide S-acetyltransferase (DLAT) and the reduction of iron–sulfur cluster (Fe–S) proteins, triggered by Cu accumulation in mitochondria, leading to proteotoxic stress, and cell death [9].
With the concept and mechanism of cuproptosis established, researchers have increasingly focused on cuproptosis in cancer therapy and demonstrated that Cu-based treatments play a pivotal role in inhibiting tumor growth. In this review, we summarized the core molecular mechanisms of cuproptosis and discussed the relationship between it and other forms of cell death. Moreover, we systematically summarized the current understanding of targeting cuproptosis for tumor therapy, including using Cu ionophores, small compounds, and nanomedicine to induce cuproptosis and targeting cell metabolism or certain genes to sensitize cuproptosis. Additionally, we discussed the potential of targeting cuproptosis to overcome tumor drug resistance in chemotherapy, targeted therapy, and immunotherapy. We also discussed the opportunities and challenges in targeting cuproptosis-associated cancer therapy.
Cu metabolism
Cu homeostasis is essential for the normal physiological functioning of human life. In humans, Cu uptake, distribution, transport, and elimination are meticulously regulated (Fig. 1A), which is crucial to prevent deficiency or excessive Cu accumulation in various tissues and cells, thereby averting disease onset [10]. Humans predominantly acquire Cu through their diet, with an adult daily requirement ranging from 0.8 to 2.4 mg [3]. Following digestion in the stomach and duodenum, Cu is primarily absorbed in the small intestine, where Cu2+ is reduced to Cu+ by metalloreductases, such as six-transmembrane epithelial antigen of the prostate (STEAP) [11] and duodenal cytochrome b (DCYTB) [12], before being transported into enterocytes by Cu transport protein 1 (CTR1), also known as the solute carrier family 31 member 1 (SLC31A1) [13], located at the apical membrane of enterocytes. Subsequently, Cu is exported to the interstitial fluid or bloodstream by the protein ATPase copper transporting alpha (ATP7A) [14]. Cu in the bloodstream usually binds to plasma proteins, such as ceruloplasmin and human serum albumin, and is transported to the liver, the primary Cu storage organ, via the portal system [15]. Metallothionein1/2 (MT1/2), a thiol-rich protein, binds to and stores Cu in hepatocytes [16]. Hepatocytes can excrete excess Cu into the bile via ATP7B. Beyond the liver, Cu in the bloodstream can also be absorbed by other tissues and organs, including the heart and the brain [15].
After being transported into cells by transmembrane proteins, such as CTR1 and divalent metal transporter 1 (DMT1), Cu can be stored by binding to intracellular Cu chaperones, such as MT1/2 and glutathione (GSH), thereby preventing cellular damage [1, 17]. Concurrently, Cu can be delivered to other cellular structures or proteins via Cu chaperones to maintain normal cellular function (Fig. 1B). For example, the Cu chaperone for superoxide dismutase (CCS) binds to Cu and delivers it to superoxide dismutase 1 (SOD1), catalyzing the conversion of superoxide radicals to H2O2, thus maintaining cellular ROS homeostasis [18]. Abnormal SOD1 expression is considered to be linked to tumor development [19]. Additionally, the Cu chaperone antioxidant 1 (ATOX1), which binds Cu+ via two cysteine residues, can transport cytosolic Cu+ to the ATP7A/ATP7B, located in the Golgi network [20, 21]. Excess Cu+ enters the trans-Golgi network (TGN) and can be expelled from the cell via the vesicular system [20, 21]. The absence of ATOX1 leads to perinatal lethality induced by Cu dyshomeostasis [22]. Moreover, increased intracellular Cu levels can promote the distribution of ATP7A and ATP7B within the TGN, thereby facilitating Cu efflux [23]. These studies highlight significant regulatory roles of ATOX1 and ATP7A/B in intracellular Cu homeostasis.
The mitochondria are the primary targets of intracellular Cu (Fig. 1B). Cu contributes to ATP production within the mitochondria by ensuring the catalytic function of cytochrome oxidase (COX) during oxidative phosphorylation (OXPHOS). Cytosolic Cu+ can be transported to the mitochondrial intermembrane space by a Cu ligand (CuL), a non-proteinaceous low-molecular-weight complex, where it can enter the mitochondrial matrix via solute carrier family 25 member 3 (SLC25A3) located in the inner mitochondrial membrane (IMM) [24, 25]. Cu in the matrix is transported back across the IMM to intermembrane space (IMS) by an unknown transporter, where it is delivered to COX and SOD1 [26]. Additionally, COX17 can transfer cytosolic Cu+ to the mitochondrial intermembrane space and deliver Cu+ to other Cu chaperone molecules, such as COX11 and synthesis of cytochrome c oxidase 1/2 (SCO1/2), which then deliver Cu+ to COX1 and COX2, respectively [27, 28].
Cu and cancer
The role of Cu in tumorigenesis and tumor therapy has been of great concern. Compared to the healthy population, elevated Cu levels have been observed in the tumors or serum of patients with various types of cancers, including breast [29, 30], prostate [31], lung [32], cervical [33], and bladder [34], thyroid [35], and oral cancers [36, 37]. Cu can promote the onset and development of tumors, termed cuproplasia, by activating oncogenic signaling pathways [6]. For instance, Cu can directly bind mitogen-activated extracellular signal-regulated kinase (MEK) and activate its downstream mitogen-activated protein kinase (MAPK) pathway to promote tumor cell growth [38, 39]. In melanoma driven by BRAFV600E, chelating Cu can inhibit MAPK signal and reduce tumor cell resistance to BRAFV600E and MEK1/2 inhibitors [40]. Moreover, Cu is considered to contribute to tumor metastasis. Cu can act on metalloenzymes in the extracellular matrix, such as lysyl oxidase (LOX) [41] and secreted protein acidic and rich in cysteine (SPARC) [42], altering cell–matrix and cell–cell interactions, thereby promoting tumor cell migration and metastasis. In breast cancer cells, Cu can bind to the mediator of ErbB2-driven cell motility 1 (MEMO1) and activate its oxidase activity promoting O2− production and enhancing tumor cell migration and invasion [43, 44]. Additionally, Cu can promote angiogenesis, essential for tumor growth and progression, by activating pro-angiogenic factors, such as fibroblast growth factors (FGFs), vascular endothelial growth factor (VEGF), tumor necrosis factor alpha (TNF-α), interleukin (IL)-1, IL-6, and IL-8 [45,46,47,48]. Taken together, Cu is a critical trace metal element in tumor development. Elucidating the molecular mechanisms by which Cu drives tumorigenesis will aid the discovery of new therapeutic targets for cancer.
Cuproptosis
Although Cu-induced cell death has been investigated for decades, the concept of ‘cuproptosis’ was not proposed until 2022 by Tsvetkov and colleagues [9]. A significant feature of Cu ionophores and Cu-treated cells is a sharp increase in ROS levels, which has long been considered the main cause of cell death. ROS scavengers, such as N-acetylcysteine (NAC), can mitigate the extent of Cu-induced cell death in some cells [49,50,51,52,53]. However, eliminating ROS does not always inhibit cell death induced by Cu [9, 54], suggesting that ROS are not primary mediators of Cu-induced cell death. Tsvetkov et al. also observed that antioxidants, such as NAC, JP4-039, ebselen, and α-tocopherol, were unable to rescue cells from elesclomol (a Cu ionophore)–Cu-induced cellular damage, whereas agents that chelate Cu, such as GSH and ammonium tetrathiomolybdate (TTM), could prevent the lethality of elesclomol–Cu to cells [9]. This type of cellular damage could not be rescued by inhibitors of other types of cell death, such as apoptosis, ferroptosis, and necrosis. Tsvetkov et al. found that elesclomol could transport Cu2+ across membranes into the mitochondria, where Cu2+ was reduced to Cu+ by ferredoxin 1 (FDX1) [9], a mitochondrial matrix reductase. However, excess mitochondrial Cu+ can directly bind to lipoylated DLAT, an essential component of mitochondrial TCA cycle, causing DLAT aggregation and cytotoxicity [9]. Additionally, excess mitochondrial Cu+ reduces the stability of the Fe–S cluster proteins [9], which play an important role in OXPHOS-related electron transport. These induce proteotoxic stress, ultimately leading to cell death (Fig. 2). Pharmacological inhibition of the electron transport chain (ETC) and pyruvate uptake could reverse elesclomol–Cu-induced cell death [9], indicating that cuproptosis depends on mitochondrial respiration. Additionally, whole-genome CRISPR-Cas9 screening, combined with single-gene knockout validation experiments, showed that proteins in the lipoic acid (LA) pathway, such as FDX1, LA synthase (LIAS), lipoyl transferase 1 (LIPT1), and dihydrolipoamide dehydrogenase (DLD), and genes in the pyruvate dehydrogenase complex, such as DLAT, pyruvate dehydrogenase E1 subunit alpha 1 (PDHA1), pyruvate dehydrogenase E1 subunit beta (PDHB), metal-regulatory transcription factor-1 (MTF1), glutaminase (GLS), and cyclin-dependent kinase inhibitor 2A (CDKN2A), are important regulators of cuproptosis (Fig. 2) [9]. These results also ascertain the significance of FDX1 and its regulation of mitochondrial protein lipoylation in cuproptosis.
Cuproptosis and regulated cell death
Although Cu ionophores combined with Cu can induce cuproptosis, previous studies have also found that excessive Cu in cells can cause other ways of regulated cell death (RCD) (Fig. 3), suggesting a molecular mechanism crosstalk between cuproptosis and other forms of cell death. Understanding the role of Cu in other cell death modes can help develop more reasonable tumor treatment strategies targeting cuproptosis.
Cuproptosis and ferroptosis
Ferroptosis is a form of programmed cell death induced by disrupting iron homeostasis and accumulating ROS in lipids. Although Tsvetkov and colleagues found that the ferroptosis inhibitor ferrostatin-1 did not rescue cells from growth inhibition induced by elesclomol–Cu, Gao et al. observed that ferrostatin-1 and liproxstatin-1, another ferroptosis inhibitor, could inhibit elesclomol–Cu-induced cell damage in colorectal cancer (CRC) cells [55]. Gao et al. demonstrated that elesclomol alone treatment could reduce the ATP7A expression levels in CRC cells, potentially mediating the degradation of solute carrier family 7 membrane 11 (SLC7A11), a cysteine-glutamate transporter, resulting in lipid peroxidation and ferroptosis, suggesting that it is unclear whether elesclomol–Cu-induced ferroptosis depends on Cu [55]. Furthermore, previous studies have reported that reducing the Fe–S cluster proteins, which are the main features of cuproptosis, can induce ferroptosis [56]. Cu can exacerbate erastin-induced ferroptotic cell death in pancreatic ductal adenocarcinoma (PDAC) cells through increasing ubiquitination and aggregation of glutathione peroxidase 4, a protein blocking ferroptosis by eliminating phospholipid hydroperoxides, promoting its macroautophagic degradation [57].
These studies indicate a close interplay between cuproptosis and ferroptosis, with a key intersection being mitochondrial metabolism. As essential energy sources for cells, mitochondria play critical roles in regulating ferroptosis [58]. Cellular energy metabolic pathways, such as the TCA cycle and glycolysis, are involved in this regulation. For instance, blocking the TCA cycle or loss of glutamine can attenuate cystine-deprivation or erastin-induced ferroptosis [59], suggesting that the TCA cycle and glutaminolysis are required for ferroptosis. Similarly, in the process of cuproptosis, the TCA cycle in mitochondria is crucial [9]. The aggregation of lipoylated DLAT in the TCA cycle is a major inducer of elesclomol–Cu-mediated cell death [9]. Furthermore, cysteine-deprivation-induced ferroptosis is affected by α-ketoglutarate and other intermediates of the TCA cycle, such as succinate and fumarate [58]. Inhibition of ETC complexes can attenuate cystine-deprivation and erastin-induced lipid peroxidation and cell death [59]. Interestingly, inhibition of ETC complexes can also mitigate elesclomol–Cu-induced cuproptosis [9], suggesting that cuproptosis and ferroptosis share the same mitochondrial energy dependency.
Another important hub for cuproptosis and ferroptosis is GSH, a crucial antioxidant. GSH acts as an inhibitor of both ferroptosis and cuproptosis, indicating that it serves as a significant co-regulator in these processes. Both Cu and iron (Fe) promote the oxidation and subsequent consumption of GSH by binding to it [60]. Additionally, GSH chelates Fe and Cu to reduce metal ion toxicity [60]. Since Fe can consume GSH, over accumulation of Fe in cells may trigger cuproptosis by inhibiting GSH. GSH is also a necessary cofactor for GPX4, which reduces cytotoxic lipid peroxides (L-OOH) to corresponding alcohols (L-OH) while converting reduced GSH to oxidized glutathione (GSSG), thus reducing lipid peroxidation and inhibiting ferroptosis [61]. The accumulation of Cu in cells promotes the consumption of GSH, creating favorable conditions for ferroptosis. SLC7A11 transports glutamate outside and cystine inside cells. Cystine is then converted to cysteine, a component of GSH. SLC7A11 inhibitors, such as sorafenib and erastin, are commonly used to induce ferroptosis by reducing intracellular cysteine levels and GSH synthesis, which also makes cuproptosis more likely. Indeed, Wang et al. recently observed that sorafenib and erastin can induce cuproptosis in primary liver cancer cells by primarily reducing intracellular GSH synthesis and increasing Cu-dependent lipoylated protein aggregation [62]. Additionally, BSO, an inhibitor of GSH synthesis known to induce ferroptosis, has also been found to induce cuproptosis [9]. These studies indicate that GSH is a critical molecule mediating the crosstalk between ferroptosis and cuproptosis. Targeting GSH could be a potential strategy to simultaneously induce ferroptosis and cuproptosis in tumor cells.
ROS are also critical factors in understanding the crosstalk between ferroptosis and cuproptosis. Both Fe and Cu can produce ROS through the Fenton reaction, while rapid GSH depletion mediated by these metals can further exacerbate cellular ROS accumulation. Excessive ROS promotes lipid peroxidation and ferroptosis [63]. Although in elesclomol–Cu-induced cuproptosis, Cu toxicity primarily results from the aggregation of lipoylated proteins in the mitochondria rather than ROS production [9], excessive Cu-mediated ROS generation and GSH depletion can also contribute to ferroptosis onset. In summary, while cuproptosis and ferroptosis have distinct initiation mechanisms and molecular characteristics, they mutually influence each other, creating favorable conditions for both processes. This interplay adds complexity to their regulatory mechanisms but also offers potential advantages for cancer therapy.
Cuproptosis and apoptosis
Excessive Cu accumulation in cells has also been linked to apoptosis. For instance, treatment with CuSO4 can upregulate the C/EBP homologous protein (CHOP), Jun N-terminal kinase (JNK), and caspase-12 expression levels in mouse liver cells, thereby enhancing cell apoptosis-related signaling pathways, such as endoplasmic reticulum (ER) stress [64]. Liu et al. also found that treatment with CuSO4 can increase the ROS levels and protein carbonyl compounds in cells and decrease GSH levels, thereby activating the mitochondrial pathway of apoptosis signaling, such as cytochrome c release into the cytosol and cleavage of caspase-9 and caspase-3 [65]. In myeloma cells and osteosarcoma, disulfiram, another Cu ionophore, combined with Cu, can induce apoptosis by activating ROS and JNK signaling pathways [66, 67]. Furthermore, Cu can induce apoptosis by binding to and inhibiting 20S proteasome subunits and activating the cytochrome c-caspase cascade signaling axis [68, 69].
Before the identification of cuproptosis, the damage to tumor cells treated with Cu ionophores combined with Cu was primarily considered to result from ROS production. Excessive ROS within cells can trigger apoptosis through various pathways, including ER stress, mitochondrial damage, and activation of death receptors. In certain tumor cells, such as lung cancer cells [49, 51], gastric cancer [50], melanoma [52], and osteosarcoma [53], ROS scavengers can mitigate the cell damage induced by Cu ionophores and Cu. However, in breast cancer and glioblastoma cells [9, 54], ROS scavengers do not exhibit this protective effect. Additionally, some studies have demonstrated that Cu indeed induces apoptosis in specific tumor cells [52, 67, 70]. These studies suggest that ROS may serve as a crucial link between cuproptosis and apoptosis. Additionally, different tumor cells exhibit varying tolerance and responses to ROS, which may explain the diverse roles of apoptosis in Cu-induced cell death.
Cuproptosis and autophagy
Cu is also considered to regulate autophagy. Studies have revealed that Cu can upregulate the autophagy-related gene expression in cells, such as LC3b/LC3a, BECN1, Atg3, and Atg5 [71, 72]. Besides, Cu can directly bind to the Unc-51-like autophagy activating kinase 1/2 (ULK1/2), crucial protein kinases regulating autophagy initiation, activating ULK1/2 and its downstream autophagy pathway [73]. In KRASG12D-driven lung cancer, deletion of the Cu transporter SLC31A1 diminished the Cu-mediated activation of ULK1/2, resulting in a blockage in the autophagic flux and tumor growth suppression [73]. However, whether Cu-induced autophagy contributes to Cu toxicity remains uncertain. For instance, Tang et al. found that in ATP7B R778L mutant hepatocytes, Cu can activate autophagy, which is beneficial for inhibiting cell necrosis and reducing Cu toxicity [74]. However, in some tumor cells Cu was found to inhibit autophagy. For instance, inhibiting SLC31A1-dependent copper absorption could enhance autophagic flux of pancreatic cancer cells, leading to the suppression of tumor cell death [75]. Besides, it was found that Cu could directly bind to autophagy-related gene 4B, a crucial regulator in the autophagy process responsible for priming and delipidation of LC3, and suppress its cysteine protease activity, consequently blocking cellular autophagy [76]. These results indicate that the regulation of the autophagy process by Cu is bidirectional.
Cuproptosis and pyroptosis
Moreover, Cu can affect pyroptosis in cells. In jejunal epithelial cells, Cu can upregulate the pyroptosis-related gene expression, such as CASP1, GSDMD, and IL-1β, which is believed to be mainly mediated by the ER stress-triggered IRE1α-XBP1 pathway [77]. In hepatocytes, Cu can similarly upregulate pyroptosis-related gene expression, such as CASP1, NLRP3, IL-1β, and IL-18, and NAC and a caspase inhibitor can reverse this behavior, suggesting that ROS generated by Cu induction may be the main mediators of pyroptosis [78]. Excessive ROS can induce various types of cell death, such as apoptosis, ferroptosis, pyroptosis. Cu can induce ROS generation in numerous tumor cells, which may be a crucial factor in the cross-talk between different types of Cu-triggered RCD. This indicates that in some tumor cells highly sensitive to ROS, cuproptosis may not be irreplaceable in Cu-induced cell damage. In summary, Cu overload can cause cellular damage from multiple angles. Although this complicates the mechanism of Cu-induced cell damage, it provides more possibilities for Cu-based tumor therapy.
Targeting cuproptosis for cancer therapy
Although Cu promotes tumorigenesis to a certain extent, excessive Cu accumulation in tumor cells disrupts cellular homeostasis and induces cuproptosis. Therefore, targeting cuproptosis may be a potential tumor treatment strategy.
Induction of tumor cell cuproptosis
Cu ionophores
Cu ionophores, defined as compounds or chemicals, can bind to Cu and carry it into cells, increasing the intracellular Cu levels. As previously mentioned, the most extensively studied Cu ionophores are elesclomol and disulfiram (Table 1). Elesclomol, a highly lipophilic Cu-binding molecule, can chelate extracellular Cu2+ to form an elesclomol–Cu2+ complex, facilitating the transport of Cu into cells [145, 146]. The anti-tumor activity of elesclomol has been recognized for decades and is believed to be Cu-dependent (Table 1). Although early studies reported that cell death induced by elesclomol–Cu was linked to apoptosis and ferroptosis, Tsvetkov et al. observed that elesclomol–Cu induced cellular damage through cuproptosis [9]. Elesclomol–Cu can increase ROS levels in tumor cells [49, 54, 83], exacerbating cellular damage and suggesting that elesclomol–Cu may kill tumor cells via multiple pathways. Additionally, recent studies have revealed FDX1-independent mechanism(s) of elesclomol–associated Cu release, achieving Cu delivery to non-mitochondrial cuproproteins [147]. Whether these non-mitochondrial Cu participates in cell death other than cuproptosis induced by elesclomol–Cu requires further investigation. The crosstalk mechanisms between cuproptosis and other forms of cell death are poorly understood and necessitate more research to unveil, possibly facilitating the development of effective anticancer strategies based on elesclomol–Cu. Elesclomol has not yet shown effective therapeutic outcomes in clinical trials [148]. A possible reason is that single-agent elesclomol treatment may not elevate Cu levels in tumor cells to those required to trigger cuproptosis. A subsequent phase III trial results revealed that although the combination of elesclomol with paclitaxel did not improve progression-free survival in melanoma patients, elesclomol exhibited better anti-tumor effects in patients with low lactate dehydrogenase (LDH) levels [149]. Low LDH represents diminished glycolysis [150], reflecting enhanced mitochondrial metabolism. This aligns with Tsvetkov’s finding that cuproptosis relies on mitochondrial metabolism.
Disulfiram is an aldehyde dehydrogenase (ALDH) inhibitor FDA-approved for treating alcoholism. Disulfiram has also been deeply studied for an extended period in anti-tumor research (Table 1). Disulfiram interacts with Cu as a Cu ionophore to form the metabolite bis-diethyldithiocarbamate-Cu (CuET), which transports Cu across the cell membrane [151]. Disulfiram–Cu–induced cellular damage is also linked to apoptosis, ferroptosis, and cuproptosis (Table 1). Multiple targets or signaling pathways have been reported to be associated with the anti-tumor activity of disulfiram–Cu, such as ROS levels [94, 108, 109, 121, 122, 132, 134, 137], the ubiquitin–proteasome system [112, 124, 125, 133], the JNK and p38 pathways [66, 67, 114, 122], the NF-kB pathway [90, 92, 93, 109, 111, 122], and NPL4 [107, 127, 133]. In addition, disulfiram–Cu has been reported to overcome tumor drug resistance to cisplatin [91, 110], paclitaxel [108, 110], gemcitabine [109, 111], 5-fluorouracil (5-FU) [90, 118], temozolomide [98, 124], and sunitinib [96]. Table 1 summarizes the anti-tumor function of disulfiram in preclinical studies. Although, like elesclomol, disulfiram has presented significant anti-tumor effects in preclinical experiments, exciting results have yet to emerge from clinical trials [152, 153]. One limiting factor may be the inability to maintain high Cu levels in patient tumor cells. However, given the good clinical safety profile, conducting more clinical trials that combine elesclomol or disulfiram with clinical drugs could facilitate the translation of cuproptosis-associated anti-tumor therapies from the laboratory to clinical practice.
Besides elesclomol and disulfiram, other compounds, such as diacetyl-bis (N4-methylthiosemicarbazone) (ATSM) and glyoxal-bis (N4-methylthiosemicarbazone) (GTSM), have been identified as Cu ionophores (Table 1). Cu complexes with ATSM or GTSM induced cytotoxicity in human prostate hyperplastic and carcinoma cell lines without affecting the primary prostate epithelial cells [140]. This selective cytotoxicity may be associated with differential Cu levels in tumor cells, as Cu concentrations are elevated in prostate cancer cells compared to normal prostate epithelial cells [154]. Additionally, 7-iodo-5-chloro-8-hydroxyquinoline (CQ) has been reported to mediate Cu accumulation in cells [141]. In cancerous prostate cells, rather than normal prostate cells, CQ-Cu complexes promote apoptosis by facilitating the degradation of XIAP, a protein that inhibits caspases [141]. Notably, CQ can induce cellular damage via multiple pathways, including proteasome and lysosome dysfunction, conferring severe toxic side effects that limit its clinical application in cancer therapy [155]. Recent studies have also revealed that curcumin, a natural compound derived from Curcuma longa, can act as a Cu ionophore and promote cuproptosis in CRC cells [142, 143]. Curcumin is a potential anticancer natural product that can inhibit the cell cycle, induce apoptosis, and activate tumor suppressors. Additionally, several clinical studies have shown that curcumin has good efficacy and safety [156]. These characteristics make curcumin a promising cuproptosis inducer for clinical application. Furthermore, salicylaldehyde isonicotinoyl hydrazone (SIH), a lipophilic tridentate iron chelator, can facilitate the transportation and intracellular release of Cu2+ in HepG2 cells, thereby triggering mitochondria-mediated apoptosis, suggesting that SIH is also a Cu ionophore [144]. However, the cell death induced by these Cu ionophores, beyond elesclomol and disulfiram, whether related to the aggregation of lipoylated proteins and the reduction of Fe–S proteins, requires further investigation.
During cuproptosis, the primary function of Cu ionophores is to transport Cu across the cell membrane and release it into the cell. Notably, most metal-ion ionophores are not specific to a single metal element. For instance, elesclomol can directly bind Fe2+ [157]. Besides, elesclomol and disulfiram can increase cellular iron content during transporting Cu into cells [158, 159]. This non-specificity complicates the mechanism of cell damage caused by Cu ionophores combined with Cu. However, treatment with such agents can cause metal dyshomeostasis, exacerbating the side effects of the therapy. Consequently, developing Cu- or tumor-specific ionophores represents a potential breakthrough in accelerating the clinical application of Cu ionophores for cancer treatment.
Small compounds
Cu is a dual-faceted player in tumorigenesis. A high Cu level promotes tumor cell proliferation and growth, suggesting some resistance mechanisms to cuproptosis in tumor cells. As a result, small-molecule compounds that disrupt Cu homeostasis may also induce or increase the sensitivity of tumor cells to cuproptosis. Recent studies have unveiled several small compounds capable of inducing cuproptosis (Table 2). For instance, Yang et al. discovered that zinc pyrithione can induce cuproptosis in triple negative breast cancer (TNBC) cells by disrupting intracellular Cu homeostasis and DLAT oligomerization, potentially contributing to the chemosensitivity of TNBC [160]. In CRC cells, 4-Octyl itaconate (4-OI) inhibits glycolysis by targeting the glyceraldehyde-3-phosphate dehydrogenase (GAPDH), promoting elesclomol–Cu-mediated cuproptosis [161]. Besides, anisomycin, a well-known inhibitor of protein synthesis that binds to the 60S ribosomal subunits, has been found to bind and inhibit Yinyang 1 (YY1), inactivating the transcriptional activity of core genes of the LA pathway (FDX1, DLD, DLAT, and PDHB), potentially leading to cuproptosis in ovarian cancer stem cells [162]. Additionally, as mentioned above, sorafenib, the first multi-tyrosine kinase inhibitor approved for treating many cancers and capable of inducing ferroptosis, and erastin, a commonly used ferroptosis inducer, can aggravate cuproptosis in liver cancer cells [62]. Compared to Cu ionophores, small molecular compounds that disrupt tumor cell Cu homeostasis can induce tumor cell cuproptosis without Cu supplementation, thereby avoiding the imbalance of metal ions in the body and reducing metal-induced side effects during treatment. The cuproptosis research is currently in its infancy. The development and discovery of more cuproptosis inducers, especially those based on drugs approved for clinical use, could significantly promote the clinical application of cuproptosis-targeted cancer treatment strategies.
Nanomedicine
Dissolving, adsorption, encapsulation, or attachment to nanomatrices can transform drugs into nanomedicines. These nanomedicines use the characteristics of tumor tissues or cells, such as acidic environments, elevated GSH and ROS levels, and tumor cell-specific surface markers, to accumulate or release within tumor sites. This strategic approach can increase the precision of drug delivery and minimize the side effects of cancer therapy. Given the relatively low selectivity of Cu ionophores toward tumor cells, using a nanoparticle-based delivery system for the precise delivery of Cu to tumor cells can effectively enhance cuproptosis in tumor tissues while reducing damage to other normal tissues. Since cuproptosis was identified, more studies have focused on this area (Table 3). For instance, DSF@PEG/copper-HMSNs can precisely release Cu2+ and disulfiram in tumor tissues to induce cuproptosis and inhibit tumor growth [166]. Au NCs-Cu2+@SA-HA NHGs can enhance cuproptosis-mediated tumor therapy by depleting GSH and H2O2 in the tumor tissues [180].
Researchers have aimed to precisely deliver Cu, Cu ionophores, and other anticancer agents, such as chemotherapeutic drugs and siRNA (Table 3), to explore tumor therapy strategies based on nanomedicine-induced cuproptosis. This approach enhances cell damage through other mechanisms or sensitization to cuproptosis, thereby synergistically combating tumors. For example, TP-M–Cu–MOF/siATP7a efficiently silences the ATP7A gene and increases Cu intake, thus inducing cuproptosis and enhancing anti-tumor efficacy [178]. OMP contains siRNA targeting PDK1, which, during releasing Cu2+, can reduce cellular glycolysis by decreasing PDK1 expression, thereby sensitizing cells to cuproptosis [186]. LDH/HA/5-FU nanosheets can release 5-FU while delivering Cu2+ to tumor tissues, thus inducing apoptosis and cuproptosis in tumor cells [207].
In addition, unlike drug treatment of vitro cultured cells, nanomedicine delivered to tumor tissues impacts the tumor microenvironment (TME), an important factor influencing tumor therapy outcomes, especially in tumor immunotherapy. Nanomedicine containing Cu relies on the TME for precise delivery to tumor tissues and has the potential to modify the TME, making it more conducive to tumor therapy (Table 3). For instance, PDA-DTC/Cu NPs trigger cuproptosis in tumor cells and facilitate the repolarization of tumor-associated macrophages to mitigate the tumor immunosuppressive microenvironment (TIME) [188]. Similarly, ES@CuO promoted cuproptosis-driven immune responses and remodeled the TIME by enhancing lymphocyte infiltration and increasing the release of inflammatory cytokines within tumors. The synergistic application of ES@CuO with programmed cell death-1 (PD-1) immunotherapy markedly enhanced anti-tumor efficacy in murine melanoma models [196]. Besides, CQG NPs induce cuproptosis and pyroptosis by disrupting antioxidant defense mechanisms within tumor cells [201]. This dual action facilitates the transformation of the TIME, augments the infiltration of immune cells into the tumor, and triggers a robust systemic immune response.
Furthermore, the integration of nanomedicine with dynamic therapies, such as photothermal therapy (PTT), photodynamic therapy (PDT), and chemodynamic therapy (CDT) significantly enhances the precision and efficacy of tumor treatments. This approach represents a promising research direction for future studies on cuproptosis-associated therapeutic strategies (Table 3). For instance, PTT can augment E. coli@Cu2O-induced ferroptosis and cuproptosis, reversing the immunosuppression of colon tumors by initiating dendritic cell maturation and T-cell activation [205]. Through PTT and CDT, PEG@Cu2O-ES can generate ROS to target the ATP-Cu pump, reducing the efflux of Cu ions and exacerbating cuproptosis [208]. In nanomedicine, multiple anti-tumor components can be incorporated, significantly enhancing the medication's plasticity and multifunctionality. For instance, the CCNAs constructed by Wen et al., in addition to Cu2+, contain zinc phthalocyanine (ZnPc), 1-methyl tryptophan (1-MT), and doxorubicin (DOX) [209]. Upon near-infrared laser irradiation, ZnPc released into tumor tissues exhibited a photodynamic effect that generated ROS, effectively promoting the release of DOX and inducing apoptosis while intensifying cuproptosis [209]. Moreover, the release of 1-MT from CCNAs can reverse TIME by inhibiting IDO-1-mediated Trp degradation, triggering an immunogenic cell death (ICD) response [209].
Although nanomedicine offers broad prospects for exploring tumor treatments, numerous issues must be addressed before clinical application, warranting attention in future studies on tumor treatments based on cuproptosis. First, current experimental studies are primarily conducted in animal tumor models, which differ from primary or metastatic tumors in humans, especially regarding the tumor microenvironment. Second, the efficacy of laboratory nanomedicine in delivering human tumor tissues remains unknown. Third, research on cuproptosis-related nanomedicine has mainly focused on a limited array of cancer types in animal models, such as breast and colorectal cancers. Expanding studies on other types of tumors, particularly those that are difficult to treat, is necessary to broaden the scope of targeting cuproptosis for tumor treatment. Lastly, biosafety is a critical concern, representing a significant factor in the transition of experimental drugs to clinical applications.
Sensitization of tumor cell cuproptosis
Targeting cell metabolism sensitizes tumor cell cuproptosis
Given the close relationship between cuproptosis and cellular metabolism, targeting cellular metabolism presents a strategy to sensitize tumor cells to cuproptosis. Cuproptosis is strongly associated with mitochondrial metabolism [9]. Elevated mitochondrial metabolism can sensitize tumor cells to Cu-induced cell death. Inhibition of the mitochondrial ETC or pyruvate uptake diminishes tumor cell responsiveness to Cu ionophores [9]. This suggests that inducing cuproptosis could effectively inhibit tumor growth in cells with high aerobic respiration levels, such as melanoma [217] and leukemia [218]. Additionally, a high mitochondrial metabolic state is characteristic of tumor cell resistance to certain drugs such as proteasome inhibitors [9, 219], cisplatin [220], and 5-FU [221]. Thus, tumor cells that exhibit resistance to these drugs may be more sensitive to Cu ionophores, and inducing cuproptosis may improve treatment outcomes in patients with acquired drug resistance.
Furthermore, high glycolysis levels are considered unfavorable for cuproptosis [9], indicating that targeting glycolysis in tumor cells could also be a method to induce or sensitize cuproptosis. For instance, 4-OI attenuates aerobic glycolysis in CRC cells by targeting GAPDH, thereby sensitizing them to cuproptosis induced by elesclomol–Cu [161]. Aerobic glycolysis is the primary energy source for most tumor cells, and inhibiting glycolysis can suppress their growth [222]. This suggests that inducing cuproptosis may enhance the inhibitory effect on tumor growth during aerobic glycolysis-targeted tumor therapy. Besides, recent studies have linked cuproptosis to protein synthesis, although the mechanism remains unclear. Liu et al. found that in elesclomol–Cu-treated cancer cells, PPP1R15A could promote protein synthesis by downregulating eIF2α phosphorylation and upregulating 4EBP1 phosphorylation, thereby exacerbating proteotoxic stress [223], suggesting tumor cells with the high rate of protein synthesis might be more sensitive to cuproptosis inducers. Thus, although the relationship between cuproptosis and cell metabolism remains relatively vague and requires more basic and clinical research, the differential response of cuproptosis under various cellular metabolic states will help develop effective clinical application strategies.
Targeting cuproptosis regulatory proteins and pathways sensitizes tumor cell cuproptosis
Tsvetkov et al. identified several genes regulating cuproptosis. Among the proteins encoded by these genes, FDX1, LIAS, LIPT1, DLD, DLAT, PDHA1, and PDHB positively regulated cuproptosis, whereas MTF1, GLS, and CDKN2A negatively regulated it [9]. This suggests that these gene expression levels could serve as biomarkers of the sensitivity of tumor cells to cuproptosis. For instance, since MTF1, GLS, and CDKN2A knockout promoted cuproptosis in tumor cells, targeting these proteins or related signal pathways could represent a therapeutic sensitization strategy. Fan et al. found that plicamycin can inhibit head and neck squamous cell carcinoma (HNSCC) cell growth by targeting CDKN2A, implying that plicamycin may be a potential sensitizing agent for cuproptosis [224].
The occurrence of cuproptosis is dependent on Cu over-accumulation within cells. As previously mentioned, various factors, such as SLC31A1 and ATP7A/B, regulate cellular Cu levels [225, 226]. Since ATP7A/B can release Cu into the extracellular environment via the vesicle system [225], targeting ATP7A/B may be a means of inducing or sensitizing tumor cells to cuproptosis. For instance, Tsvetkov et al. found that in a Wilson disease mouse model, deletion of ATP7B resulted in excess Cu accumulation and cuproptosis in aging livers [9]. Additionally, Zhang et al. used nanoparticles to simultaneously deliver Cu and ATP7A-specific siRNA to small-cell lung cancer brain metastasis tumors, enhancing cuproptosis and tumor growth suppression [178]. Although an increase in intracellular Cu can promote ATP7A/B-dependent Cu efflux, Cu ionophores have been found to reduce ATP7A/B expression levels. For example, elesclomol and disulfiram could reduce the ATP7A expression level in CRC and prostate cancer cells, respectively [55, 139]. This suggests that Cu ionophores can transport Cu into cells while reducing Cu efflux, providing favorable conditions for inducing cuproptosis.
Although research into the mechanisms of cuproptosis remains in its initial stages, recent studies have uncovered several key regulatory factors of cuproptosis. For instance, in hepatocellular carcinoma (HCC) cells, maternal embryonic leucine zipper kinase (MELK) can enhance DLAT expression by activating the PI3K/mTOR signaling pathway, thereby augmenting mitochondrial function [227]. MELK overexpression exacerbates elesclomol–induced cuproptosis and enhances its anti-tumor effects [227]. Mucin 20 (MUC20) overexpression in proteasome inhibitor-resistant multiple myeloma cells can induce cuproptosis, which is associated with the reduced cuproptosis inhibitor CDKN2A expression level [228]. Elesclomol–Cu activates the adenosine 5′-monophosphate (AMP)-activated protein kinase (AMPK) signaling pathway in non-small cell lung cancer (NSCLC) cells, attenuating the cuproptosis [229]. Knocking down or inhibiting AMPK can aggravate elesclomol–Cu-induced cuproptosis [229]. Besides, in gastric cancer cells, METTL16 can promote cuproptosis by facilitating FDX1 accumulation via m6A modification of FDX1 mRNA [230]. Further studies revealed that Sirtuin 2 (SIRT2) can inhibit METTL16 activity via deacetylation, and inhibiting SIRT2 can significantly enhance the anti-tumor effect of elesclomol–Cu in gastric cancer [230]. Additionally, some cuproptosis inhibitory factors have been identified in different tumor cells, such as SLC7A11 [231] and AT-rich interactive domain 1A (ARID1A) [232] in liver cancer cells, trigger transposable element-derived 1 (TIGD1) in CRC [233], and Wiskott-Aldrich syndrome protein family member 2 (WASF2) in ovarian cancer cells [234]. Targeting these factors may sensitize tumor cell cuproptosis and enhance the efficacy of tumor treatment.
Recently, extracellular signaling molecules have also been found to be involved in regulating cuproptosis. For example, in diabetic mice, an increase in blood advanced glycosylation end products (AGEs) and Cu upregulates SLC31A1 expression level in cardiomyocytes, thereby disturbing Cu homeostasis and promoting cuproptosis [235], suggesting that AGEs may be sensitizers for cuproptosis. Moreover, adrenomedullin (ADM), a member of the amylin/calcitonin gene-related peptide superfamily, has been found to promote the phosphorylation and nuclear translocation of Forkhead box O3 (FOXO3) via the p38/MAPK signaling pathway, thereby inhibiting FDX1 transcription and suppressing cuproptosis in renal cell carcinoma (RCC), promoting chemoresistance [236]. Consequently, targeting cuproptosis-related cytokines in the blood is also a strategy to sensitize tumor cells to cuproptosis. Table 4 lists the regulatory proteins and pathways of cuproptosis, which are potential targets for sensitizing Cu-induced tumor cell death.
Targeting cuproptosis to overcome tumor drug resistance
As the duration of drug usage extends, tumor cells may develop resistance to therapeutic agents, diminishing drug efficacy and leading to tumor relapse or progression. Therefore, effectively overcoming cancer drug resistance has always been a significant theme in cancer treatment research. Since cuproptosis has been established as a novel mode of cell death, targeting tumor cell cuproptosis holds potential as a new strategy to overcome tumor drug resistance.
The use of Cu ionophores to overcome tumor chemotherapeutic drug resistance has a long history of research. On one hand, Cu ionophores can transport Cu into the cells to induce Cu-triggered cell damage, thereby exacerbating the death of resistant cells (Table 1). For instance, in prostate cancer, elesclomol–Cu can enhance sensitivity to docetaxel by inducing DLAT/mTOR pathway-dependent cuproptosis in vitro and in vivo [87]. Disulfiram–Cu has been found to sensitize breast cancer cells to paclitaxel by simultaneous induction of ROS and inhibition of NF-κB, suggesting its potential to overcome clinical resistance to paclitaxel [108]. Disulfiram–Cu can enhance the cytotoxicity of gemcitabine by reversing NF-κB activity in gemcitabine-resistant colon cancer cells [111]. Moreover, disulfiram–Cu was found to overcome bortezomib and cytarabine resistance in cell lines from patients with Down syndrome-associated acute myeloid leukemia, which is thought to be associated with the induction of apoptosis and re-inhibition of proteasome activity [138]. In addition to Cu ionophores, small molecule compounds capable of inducing cuproptosis are potential candidates for overcoming tumor treatment resistance. These compounds usually enhance anti-tumor effects by inducing cell damage through multiple mechanisms. For example, zinc pyrithione induces necrosis in prostate cancer cells by activating the PKC and ERK pathways and enhancing ROS production [239]; 4-OI induces ferritinophagy-dependent ferroptosis in multi-drug resistant retinoblastoma cells [240]. Among these compounds, the ferroptosis inducer erastin has garnered significant attention for its ability to reverse the resistance of various tumor cells to chemotherapeutic drugs, including ovarian cancer [241, 242], AML cells [243], NSCLC cells [244], and prostate cancer cells [245]. However, whether cuproptosis contributes to the sensitizing effects of these drugs requires further investigation. Future research should explore combining these compounds with chemotherapeutic drugs to treat drug-resistant tumor cells that are sensitive to cuproptosis. Additionally, nanomedicine-based targeting of cuproptosis can be examined to overcome chemotherapeutic drug resistance. For instance, CuO2/DDP@SiO2, which releases Cu2+ and cisplatin, can induce cuproptosis and block the entire cisplatin efflux pathway by downregulating multidrug resistance-associated protein 2 (MRP2), enhancing the anti-tumor effect of cisplatin [193]. E-C@DOX NPs can inhibit tumor cell stemness and cell survival-related pathways while working with Cu ions to damage mitochondria and induce cuproptosis, suppressing the ATP-dependent drug efflux pathway and reversing DOX resistance [204].
Notably, Cu ionophores also chelate certain drugs, especially platinum-based drugs, which are widely used as first-line clinical treatments for cancer. Disulfiram has been found to form a new platinum (Pt) chelate, Pt(DDTC)3+, which has a stronger anti-NSCLC effect than cisplatin alone [105]. Furthermore, Pt drugs and Cu share molecular mechanisms for intracellular transport and extracellular efflux, such as the Cu transporter CTR1, which can transport Pt into the cell [246, 247], and the Cu chaperone protein ATOX1, which can deliver Pt to ATP7A/B located on TGN, thereby promoting the efflux of Pt and leading to drug resistance during treatment [248,249,250]. Thus, targeting Cu homeostasis can also alter the intracellular Pt drug concentration, a potential mechanism for overcoming resistance. Yuki et al. found that in bladder cancer cells treated with disulfiram and cisplatin, disulfiram could reduce ATP7A expression level and its localization in the TGN, accumulating intracellular cisplatin and enhancing tumor cell death [251]. However, increased Cu levels reduce the expression or activity of Cu uptake proteins, such as CTR1, and enhance the translocation of ATP7A/B from the Golgi to post-Golgi sites or lysosomes to promote Cu efflux, which may be unfavorable for accumulating Pt drugs within cells [252,253,254,255]. Therefore, targeting Cu homeostasis to overcome tumor cell resistance to Pt drugs requires comprehensive consideration of the dosage of Pt drugs and the action of cuproptosis.
Moreover, targeted cuproptosis could be used to solve the problem of drug resistance in targeted therapies. For example, disulfiram–Cu kills and sensitizes BRAF-mutant thyroid cancer to BRAF kinase inhibitor by relieving feedback activation of the MAPK/ERK and PI3K/AKT pathways in a ROS-dependent manner [134]. In HCC cells, researchers observed that disulfiram–Cu could strengthen the cytotoxicity of sorafenib by simultaneously inhibiting the NRF2 and MAPK kinase signaling pathways and arrest tumor growth in vitro and in vivo [136]. Current research on cuproptosis overcoming drug resistance in tumor-targeted therapy remains relatively limited. One of the main reasons is that the molecular regulation mechanism underlying cuproptosis remains unknown. However, the relationship between tumor drug resistance and cuproptosis remains unclear, hindering the progress of targeting cuproptosis to overcome drug resistance in tumor-targeted therapy.
Targeting cuproptosis to enhance tumor immunotherapy
Immunotherapy has become an important clinical strategy for cancer treatment due to its significant efficacy in tumor therapy. Since Cu metabolism and cuproptosis play crucial regulatory roles in tumor immunity, targeting cuproptosis may represent a vital sensitization strategy for tumor immunotherapy. PD-1/ PD-L1 (Programmed death-ligand 1) serves as a crucial immune checkpoint, and inhibiting or eliminating PD-1/PD-L1 can lead to favorable clinical outcomes in patients with cancer [256]. Cu may exert a positive regulatory effect on PD-L1 expression in tumors. For instance, disulfiram–Cu can upregulate PD-L1 expression in HCC cells by inhibiting Poly (ADP-ribose) polymerase 1 (PARP1) activity and promoting glycogen synthase kinase 3β (GSK-3β) phosphorylation, thereby suppressing T-cell infiltration [135]. Hence, simultaneous targeting of cuproptosis and co-administration of PD-1/PD-L1 inhibitors may enhance therapeutic effects. This notion is supported by preclinical studies demonstrating superior tumor growth inhibition when Cu ionophores were combined with Cu and anti-PD-L1 agents in PDAC [102], lung cancer [106], and HCC cells [135].
The TME is a pivotal determinant of the efficacy of tumor immunotherapy. Reshaping the immunosuppressive TME, such as dendritic cell maturation and activation of CD8+ T cells, is poised to enhance tumor suppression [257]. The cyclic GMP-AMP synthase (cGAS)-stimulator of interferon genes (STING) signaling pathway is a critical component of innate immunity, capable of sensing aberrant DNA and triggering the release of type I interferons, thereby promoting dendritic cell maturation and migration, as well as augmenting the cytotoxic effects of T lymphocytes or natural killer cells [258]. Jiang et al. demonstrated that elesclomol–Cu-induced cuproptosis in clear cell RCC can activate the cGAS-STING pathway within dendritic cells, thereby promoting the release of inflammatory mediators, including IFN-γ, TNF-α, IL2, C-X-C motif chemokine ligand 10 (CXCL10), and CXCL11, ultimately enhancing tumor immunotherapy [259]. Additionally, CS/MTO-Cu@AMI, established by Huang et al., can activate anti-tumor immunity by inducing dsDNA damage and activating the cGAS-STING pathway [173]. Similarly, PCM nanoinducers constructed by Dai et al. can trigger the release of mitochondrial DNA during inducing tumor cell cuproptosis, activating the cGAS-STING pathway and stimulating innate and adaptive immune responses, thereby enhancing tumor suppression [184].
As discussed in this review, nanomedicine-based cuproptosis induction systems mediate tumor cell cuproptosis and impact the TME by depleting GSH, aggravating oxidative stress, and inducing other types of cell damage, such as pyroptosis and apoptosis. These alterations result in the remodeling of the TME and initiation of ICD responses, which are conducive to enhanced immunotherapy. Consequently, inducing cuproptosis may represent an effective strategy for sensitizing tumors to immunotherapy. Table 3 summarizes various nanomedicines, such as NP@ESCu [171], BCMD [176], OMP [186], PCD@CM [195], ES@CuO [196], CBS [203], E. coli@Cu2O [205], PEG@Cu2O-ES [208], and CLDCu [213], in combination with anti-PD1 or anti-PD-L1 antibodies, effectively inhibited tumor growth. However, several issues must be addressed before these strategies are applied clinically. For instance, the mechanisms underlying cuproptosis-mediated TME remodeling remain unclear. Additionally, are the induction conditions and regulatory mechanisms of cuproptosis in tumors and immune cells similar or different? How can we target tumor cell cuproptosis more precisely to initiate ICD responses? Addressing these problems holds promise for improving the effectiveness of tumor immunotherapy.
Conclusions and future perspectives
Cuproptosis, characterized by its unique features, represents a novel mode of cell death that has infused new optimism into cancer treatment. Since its conceptualization, cuproptosis has received significant attention in oncology. Conversely, it has emerged as a promising therapeutic target, with ongoing research poised to unveil additional cuproptosis inducers, including small-molecule compounds and nanomedicines. This expanding repertoire of therapeutic options holds the potential to diversify tumor treatment strategies. Targeting cuproptosis offers a novel approach to combatting tumor drug resistance. Exploiting therapeutic-induced metabolic changes in tumor cells, such as heightened mitochondrial metabolism and glycolysis, rendering them susceptible to cuproptosis, provides a pathway to sensitize tumor cells to drug interventions or overcome drug resistance. Furthermore, inducing cuproptosis in tumor tissues can remodel the tumor microenvironment, fostering dendritic cell maturation and immune cell infiltration. Consequently, targeting cuproptosis promises to enhance the response rates and overcome resistance to immunotherapy.
However, understanding and research regarding cuproptosis are still in their infancy. Before practical application, numerous issues must be addressed. For instance, Cu can play a dual role in tumor initiation and progression, promoting tumorigenesis and inducing cell death [260, 261]. Cu chelators reduce Cu bioavailability and exert anticancer effects [262]. Therefore, comprehending how tumor cells balance the dual effects of Cu is crucial. Furthermore, whether cuproptosis or its related signaling pathways have pro-tumor effects during tumor initiation, development, and treatment remains unclear. In addition, reliable biomarkers, initiation mechanisms, and links with other cell death forms for cuproptosis remain lacking, impeding the progress of cuproptosis-associated research in diseases and targeted clinical applications. Moreover, distinguishing between the regulatory mechanisms of cuproptosis in normal and tumor cells is crucial for improving the precision of cuproptosis-targeted therapy and reducing the side effects of treatment. Additionally, currently widely used cuproptosis inducers, such as Cu ionophores elesclomol and disulfiram, have not revealed promising therapeutic effects in clinical trials.
Based on the challenges outlined above, the following recommendations may help promote the translation of cuproptosis-associated anti-tumor therapies from the laboratory to clinical practice in future research. First, unraveling the molecular mechanisms underlying tumor cell tolerance and exploiting high Cu levels may offer insights into inducing cuproptosis by disrupting endogenous Cu metabolism within tumor cells. For example, hepatocytes are the primary storage cells for Cu, and abnormal Cu accumulation in liver cells, as observed in patients with Wilson's disease, promotes the development of HCC [263]. Accordingly, driving accumulated Cu in HCC cells to induce cuproptosis might reverse the pro-carcinogenic effects of Cu to anticarcinogenic effects. Additionally, future research and development efforts should focus on novel cuproptosis inducers or induction strategies, including natural products, small-molecule compounds, and nanomedicine. Furthermore, improving the precision of drug delivery to tumor cells and the stability of drugs in plasma should be a priority in the development of cuproptosis inducers. Moreover, conducting more clinical trials is crucial for promoting the clinical application of cuproptosis-targeted therapies. For example, combining Cu ionophores with frontline clinical drugs that can enhance sensitivity to cuproptosis might address issues of drug resistance during treatment. Finally, similar to other types of cell death, inducing cuproptosis to treat tumors will also face the drug resistance issues. Therefore, uncovering the mechanisms of cuproptosis-related drug resistance, particularly in different tumor cell types, should be a key focus of future research.
In summary, cuproptosis is a new target in cancer treatment. As the regulatory mechanisms of cuproptosis continue to be elucidated and the efficiency of cuproptosis induction methods improves, targeting cuproptosis presents a promising new approach to combat chemotherapy and immunotherapy resistance in cancer treatment, leading to improved therapeutic outcomes.
Availability of data and materials
No datasets were generated or analysed during the current study.
Abbreviations
- ROS:
-
Reactive oxygen species
- DLAT:
-
Dihydrolipoamide S-acetyltransferase
- TCA:
-
Tricarboxylic acid
- STEAP:
-
Six-transmembrane epithelial antigen of the prostate
- DCYTB:
-
Duodenal cytochrome b
- CTR1:
-
Cu transport protein 1
- SLC31A1:
-
The solute carrier family 31 member 1
- ATP7A:
-
ATPase copper transporting alpha
- MT1/2:
-
Metallothionein1/2
- GSH:
-
Glutathione
- SOD1:
-
Superoxide dismutase 1
- ATOX1:
-
Antioxidant 1
- TGN:
-
Trans-Golgi network
- COX:
-
Cytochrome oxidase
- OXPHOS:
-
Oxidative phosphorylation
- MEK:
-
Mitogen-activated extracellular signal-regulated kinase
- MAPK:
-
Mitogen-activated protein kinase
- FGFs:
-
Fibroblast growth factors
- VEGF:
-
Vascular endothelial growth factor
- TNF-α:
-
Tumor necrosis factor alpha
- NAC:
-
N-Acetylcysteine
- TNBC:
-
Triple negative breast cancer
- AMPK:
-
Adenosine 5′-monophosphate (AMP)-activated protein kinase
- ES:
-
Elesclomol
- FDX1:
-
Ferredoxin 1
- ETC:
-
Electron transport chain
- LA:
-
Lipoic acid
- LIAS:
-
LA synthase
- LIPT1:
-
Lipoyl transferase 1
- DLD:
-
Dihydrolipoamide dehydrogenase
- PDHA1:
-
Pyruvate dehydrogenase E1 subunit alpha 1
- PDHB:
-
Pyruvate dehydrogenase E1 subunit beta
- MTF1:
-
Metal-regulatory transcription factor-1
- GLS:
-
Glutaminase
- CDKN2A:
-
Cyclin-dependent kinase inhibitor 2A
- RCD:
-
Regulated cell death
- CRC:
-
Colorectal cancer
- SLC7A11:
-
Solute carrier family 7 membrane 11
- PDAC:
-
Pancreatic ductal adenocarcinoma
- ER stress:
-
Endoplasmic reticulum stress
- DSF:
-
Disulfiram
- ULK:
-
Unc-51-like autophagy activating kinase
- 5-FU:
-
5-Fluorouracil
- 4-OI:
-
4-Octyl itaconate
- HCC:
-
Hepatocellular carcinoma
- TME:
-
Microenvironment
- TIME:
-
Tumor immunosuppressive microenvironment
- PD-1:
-
Programmed cell death-1
- PD-L1:
-
Programmed death-ligand 1
- PTT:
-
Photothermal therapy
- PDT:
-
Photodynamic therapy
- CDT:
-
Chemodynamic therapy
- DOX:
-
Doxorubicin
- ZnPc:
-
Zinc phthalocyanine
- 1-MT:
-
1-Methyl tryptophan
- ICD:
-
Immunogenic cell death
- HNSCC:
-
Head and neck squamous cell carcinoma
- NSCLC:
-
Non-small cell lung cancer
- MELK:
-
Maternal embryonic leucine zipper kinase
- cGAS:
-
Cyclic GMP-AMP synthase
- STING:
-
Stimulator of interferon genes
- CXCL:
-
C-X-C motif chemokine ligand
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We thank Home for Researchers editorial team (www.home-for-researchers.com) for language editing service.
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This work was supported by the National Natural Science Foundation of China (Grant Numbers: 32000533); Sichuan Science and Technology Program (Grant Number: 2021YFS0215).
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C. Z. contributed to conception and design of the manuscript; C. Z. and T. H. drafted the manuscript and conducted image processing. L. L. contributed to reviewing. C. Z. given the final approval of the version to be published.
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Zhang, C., Huang, T. & Li, L. Targeting cuproptosis for cancer therapy: mechanistic insights and clinical perspectives. J Hematol Oncol 17, 68 (2024). https://doi.org/10.1186/s13045-024-01589-8
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DOI: https://doi.org/10.1186/s13045-024-01589-8