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. 2021 May 18;12:624725. doi: 10.3389/fimmu.2021.624725

Table 1.

MiRNA related with MDSC in tumor progression.

MiRNA Status Target MiRNA’s regulating in TAM Impact on tumor progression
MiR-155 Increased FGF2 Enhance suppressive function Suppress the cell viability, migration and invasion (32)
MiR-98 Increased IL-10 Inhibit the function of TAM Suppress migration and invasion of hepatocellular carcinoma cells (28)
Let-7a Increased STAT3 NF-κB Suppress macrophage infiltrations and malignant phenotype Decrease tumor growth (33)
MiR-30a Increased Twist1 Vimentin Inhibit the function of TAM Promote metastatic potential of bladder cancer (34)
MiR-25- 3p MiR-130b-3p MiR-425-5p Increased PTEN Induce M2 polarization Promote cancer metastasis (35)
MiR-125a Increased HIF-1α IRF4 Increase phagocytic activation Repress tumor growth (36)
MiR-145 Increased histone deacetylase 11 Polarize macrophage-like cells into the M2-like phenotype Enlarge the tumor volumes (20)
MiR-142-3p Increased RAC1 Propofol stimulates TAM to secrete miR-142-3p Inhibit HCC cell invasion (37)
MiR-21 Increased PI3K/ AKT Enhance the function of M2 TAM Suppress cell apoptosis and confer cisplatin resistance in gastric cancer (38)
MiR-100 Increased mTOR Maintain the phenotype of TAMs Promote tumor metastasis (18)
MiR-125b Increased CSF1/CX3CL1 Decrease the abundance of TAM Alleviate the tumor growth (39)
MiR-1246 Increased Reprogram macrophages to a tumor supportive and anti-inflammatory state Promote colon cancer progression and metastasis (22)
MiR-375 Increased TNS3 PXN Enhance macrophage migration and infiltration Develop a tumor-promoting microenvironment (19)
MiR-720 Increased GATA3 Suppress M2 macrophage polarization Inhibit migration of breast carcinomas (40)
MiR-221-3p Increased CDKN1B Enhance function of TAM Contribute to the proliferation and G1/S transition of epithelial ovarian cancers (41)
MiR-125b-5p Increased LIPA Induce a tumor-promoting TAM phenotype Promote tumor development (42)
MiR‐30c Increased REDD1 Promote M1 macrophage differentiation (43)
MiR‐362‐3p Increased CD82 M2 macrophages mediate overexpression of miR‐362‐3p Promote epithelial‐mesenchymal transition in hepatocellular carcinoma cells (30)
MiR-155 Decreased C/EBPb Promote tumor-activated monocytes to produce cytokine (44)
MiR-34a Decreased VEGF TAM release TGF-β to downregulate miR-34a Improve the proliferation and invasion of colorectal cancer (27)
MiR- 4319 Decreased NECAB3 Promote M2 macrophage polarization Promote Non-small cell lung cancer progression (45)
MiR-21 Increased SNAI1 MRC1 Suppress M1 markers and enhance M2 markers Promote tumor angiogenesis and growth (21)
MiR-101 Increased DUSP1 Regulate macrophage to innate immune responses Promote hepatocarcinoma growth and metastases (46)
MiR-222-3p Increased SOCS3 Induce polarization of the M2 phenotype As a biomarker of epithelial ovarian cancer (47)
MiR-106b-5p Increased IRF1/IFN-β Promote M2 polarization Enhance glioma growth (48)
MiR-17 MiR-20a HIF-2a Enhance proangiogenic Contribute to the angiogenic process within tumors (29)
MiR-30e* Decreased Bmi1 Enhance the regulation mediated by TAM Promote tumor growth, invasion, and metastasis of gastrointestinal cancer (49)
MiR-146a MiR-222 Decreased NF-κB p50 subunit Promote the phenotype molecules of M2 macrophage Enhance TAM chemotaxis Promote tumor growth (50)
MiR let-7b Decreased Modulate macrophage polarization Reduce angiogenesis and prostate carcinoma (51)
MiR-125a/b Decreased CD90 Enhance the function of TAM Promote HCC cell proliferation and stem cell properties (31)