Table I.
Factor | Receptor | Pathways/key genes | Function | (Refs.) |
---|---|---|---|---|
Leptin | OBR | ER signal, JAK/STAT3, PI3K/AKT, IL-1/IL-1R, VEGF/VEGFR, FAK and SRC-1/STAT3 | Proliferation, differentiation, metastasis, self-renewal and chemoresistance and angiogenesis | (52,90,93–98) |
Adiponectin | AdipoR1/AdipoR2 | ERK1/2, AKT, TNFα, IL-1β, NF-κB, IL-6, IL-8, STK11 and AMPK/ULK1, AMPK and PI3K/AKT | Negatively regulating cancer cell growth, autophagy, inhibiting proliferation and invasion | (5,101) |
CCL2 | CCR2/4 | Notch1, CXCL12 and CLS | Inducing the activity of CSCs, inflammation and malignant progression | (111–114) |
CCL5 | CCR5 | ERK, EMT, AKT/mTOR | Inflammation, poor DFS and OS | (119,120,123) |
IL-6 | IL-6R/gp130 | NF-κB, STAT3, EMT | Migration, proliferation, invasion and pro-inflammatory response | (134,135,138) |
CCL, chemokine (C-C motif) ligand; CCR, C-C chemokine receptor type; OBR, leptin receptor; AdipoR, adiponectin receptor; IL-6R, IL-6 receptor; gp130, glycoprotein 130; ER, estrogen receptor; JAK, Janus kinase; IL-1R, IL-1 receptor; FAK, focal adhesion kinase; SRC-1, steroid receptor coactivator-1; STK11, serine/threonine kinase 11; AMPK, adenosine 5′-monophosphate-activated protein kinase; ULK1, Unc-51 like autophagy activating kinase; CXCL12, chemokine (C-x-C motif) ligand 12; CLS, crown-like structure; CSC, cancer stem cell; EMT, epithelial-mesenchymal transition; DFS, disease-free survival; OS, overall survival.