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. 2022 Jun 23;5(3):762–793. doi: 10.20517/cdr.2022.18

Table 2.

miRNAs regulating mechanisms of drug resistance, autophagy, cancer stem cells, and signaling pathways

miRNA Alteration Target gene Mechanism Effect on resistance Drug
Reference
miR-124

Downregulation
ATMIN
PARP1
DNA damage response Increase CPT, VP‐16, and DOX [173]

miR-15b Downregulation WEE1 DOX [184]
miR‐101
Downregulation
ATG4,5 Blockage of
autophagy
Increase DOX [185]
miR‐22
Downregulation
HMGB1
Increase DOX and cisplatin [186,187]
miR‐30a
Downregulation
BECN1 Increase DOX [188]
miR‐199a‐5p Downregulation
BECN1 Increase Cisplatin [189]
miR‐155
Upregulation ATG5 Induction of autophagy Increase DOX and cisplatin [190]
miR‐140‐5p Upregulation IP3K2 Increase DOX and cisplatin [182]
miR‐143
Downregulation ATG2B
BCL2
LC3-II
Activation of autophagy and stem cells Increase DOX [191]
miR‐let‐7d
Downregulation or Upregulation
HMGA2
Lin28B
Nanog
Oct3,4
Sox2
Induction of EMT and plastic transition of CSC Increase DOX, cisplatin, VP-16, paclitaxel [192]
miR‐29b‐1 Downregulation CD133
N-Myc
Nanog
Oct3,4
Sox2
Reduction of CSC Increase DOX, cisplatin, and VP‐16 [193]
miR‐34c
Downregulation NOTCH1 LEF1 Inhibition of metastasis Increase DOX, cisplatin, and MTX [194]
miR‐34b
Downregulation PAK1
MDR1
Induction of cell apoptosis Increase DOX, GEM, and MTX [195]
miR‐497
Downregulation VEGFA
Inhibition of proliferation Increase Cisplatin [196]
miR‐221
Upregulation
PTEN
Promotion of proliferation and inhibition of apoptosis Increase Cisplatin [197]
miR‐146b‐5p Upregulation
ZNRF3 Induction of migration and metastasis Increase DOX, cisplatin, and MTX [198]
miR-488 Upregulation BIM

Promotion of proliferation, reduction of apoptosis Increase DOX [199]
miR-765 Downregulation APE-1 Inhibition of DNA damage response Decrease Cisplatin [179]
miR-21 Upregulation Spry1, Spry2
PTEN
Inhibition of migration/proliferation Decrease Cisplatin [200]
[201]
miR-138 Downregulation EZH2 Inhibition of migration/proliferation Decrease Cisplatin [180]
miR-140-5p Downregulation IP3K2 Induction of cell apoptosis Decrease DOX and cisplatin [182]
miR-184 Upregulation BCL2L1 Inhibition of cell apoptosis Decrease DOX [183]
miR-367 Upregulation BAX, cleaved CASP3, KLF4 Promotion of metastasis and EMT Decrease DOX [181]

APE-1: Apurinic endonuclease; ATG2B: autophagy-related 2B protein; ATMIN: ataxia telangiectasia mutated interactor; BAX: BCL2 associated X; BCL2: B-cell lymphoma 2 protein; BCL2L1: BCL2-like 1; BECN1: beclin 1; BIM: B-cell lymphoma-like protein 11; CASP3: caspase 3; CPT: camptothecin; CD133: prominin-1; CSC: cancer stem cells; DOX: doxorubicin; EMT: epithelial-to-mesenchymal transition; EZH2: enhancer of zeste 2 polycomb repressive complex 2 subunit; GEM: gemcitabine; HMGA2: high mobility group AT-hook 2; HMGB1: high‐mobility group box 1; IP3K2: inositol 1,4,5‐trisphosphate kinase 2; KLF4: Kruppel-like factor 4; LC3-II: light chain 3 type II protein; LEF1: lymphoid enhancer‐binding factor 1; LIN28B: lin-28 homolog B; MDR1: multidrug resistance 1; MTX: methotrexate; Nanog: Nanog homeobox; N-myc: mycn proto-oncogene; NOTCH1: Notch receptor 1; Oct 3 and 4: octamer-binding transcription factor 3 and 4; PAK1: p21‐activated protein kinase 1; PARP1: poly(ADP‐ribose) polymerase 1; PTEN: phosphatase and tensin homolog; RAB10: Ras-related protein 10; Sox2: SRY-box transcription factor 2; Spry1 and -2: sprouty; VEGFA: vascular endothelial growth factor A; VP‐16: etoposide; ZNRF3: zinc and ring finger 3.