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Table 2 Key inflammatory cytokines involved in cancer

From: Targeting inflammation as cancer therapy

Inflammatory cytokines

Major sources

Receptors

Key actions in cancer

TNF-α

Macrophages, T lymphocytes, NK cells, neutrophils, mast cells, eosinophils and neurons

TNF-αR-1, TNF-αR-2

•Antitumor actions by promoting tumor cell apoptosis, directing TAMs toward the M1 phenotype, and impairing tumor vasculature

 

•Promotes the EMT of tumor cells

 

•Immunosuppressive actions by promoting Tregs survival and functions

TGF-β

Tumor cells, bone matrix

TGF-βRI, TGF-βRII

•Suppresses cancer at early stages of tumorigenesis through apoptosis induction and immune cell modulation

 

•Facilitates cancer progression at the later stage by promoting EMT, immune escape, angiogenesis, and suppressing apoptosis

IFN-I

DCs, B cells, fibroblasts

IFNAR1, IFNAR2

•Provides proinflammatory signals for tumor progression

 

•Facilitates immune evasion of tumor cells

 

•Promotes cancer stemness by triggering the epigenetic regulator

 

•Antitumor activities by negatively regulating premetastatic niche formation in the TME

IL-1

Tumor cells, MDSCs, TAMs, TANs, regulatory B (Breg) cells and Th17

IL-1R

•Promotes tumor progression by recruiting MDSCs to inhibit T cell activation

 

•Promotes the production of angiogenic factors such as VEGF by tissue-resident endothelial cells

 

•Antitumor activities by inducing Th1-mediated immunity against cancer

IL-6

Tumor cells, T cells, B cells, monocytes, fibroblasts, keratinocytes, endothelial cells, mesangial cells, adipocytes

IL-6R

•Promotes tumor progression by inducing tumor cell proliferation, survival, EMT, angiogenesis, and chemoresistance

 

•Suppresses tumor cell senescence

IL-10

Tumor cells, leukocytes

IL-10R

•Contributes to immunosuppressive microenvironment via exhaustion of intratumoral CD8 + T cells

 

•Antitumor activities by promoting the infiltration and cytotoxic activity of CD8 + T cells

  1. TGF-β, transforming growth factor-β; TGF-βR, TGF-β receptor; IL, interleukin; IFN, interferon; TNF, tumor necrosis factor; DC, dendritic cell