From: Recent advances of m6A methylation modification in esophageal squamous cell carcinoma
Related tumors | m6A regulator | Roles | Study model | Mechanism | Resistance | Ref. |
---|---|---|---|---|---|---|
Breast cancer | METTL3 | Oncogene | In vitro: MCF-7 | METTL3, hepatitis B virus X protein binding protein (HBXIP) and miRNA let-7Â g form a positive feedback loop | Tamoxifen | [41] |
ALKBH5 | Oncogene | In vivo: mice | Demethylation of NANOG and increase of mRNA level | [42] | ||
Ovarian cancer | YTHDF1 | Oncogene | In vitro: SKOV3, A2780 | TRIM29 may be used as an oncogene | Cisplatin | [43] |
FTO/ALKBH5 | Oncogene | In vitro: PEO1 | Up-regulation of Wnt/ β-catenin pathway by stabilizing FZD1 | Olaparib | [44] | |
Cervical cancer | FTO | Oncogene | In vitro: SiHa | Regulation of β-catenin/ERCC1 axis | – | [45] |
Acute myeloid leukemia (AML) | METTL3 | Oncogene | In vitro: MOLM13, THP-1, MV4-11, NOMO-1, HL-60, EOL-1, KG-1, RN2c, HEL, JURKA T, LOUCY, K562 | Regulating the expression of c-Myc, Bcl-2 and PTEN | – | [46] |
METTL14 | Oncogene | In vivo: human | Enhanced self-renewal of hematopoietic stem cells and inhibition of bone marrow cell differentiation through SPI1-METTL14-MYB/MYC axis | – | [47] | |
WTAP | Oncogene | In vitro: K562,HL-60,OCI-AML3,Ba/F3 | Regulating WT1 pathway to promote cell proliferation | – | [48] | |
Glioblastomas (GBMs) | METTL3 | Oncogene | In vivo: human | Inhibition of tumorigenesis and self-renewal / proliferation of MSCs | Y- Irradiation | [49] |
METTL14 | Suppressor | In vivo: human | It is possible to target ADAM19 to inhibit tumorigenesis and self-renewal / proliferation of glioma stem-like cells (GSCs) | – | [50] | |
FTO | Oncogene | In vivo: human | The inhibitory effect of drugs on FTO can inhibit the formation of m6A demethylation gene in glioblastoma | – | [50] | |
ALKBH5 | Oncogene | In vivo: mice | Demethylated FOXM1 promotes tumorigenicity of GSC | – | [51] | |
Non-small cell lung cancer (NSCLC) | METTL3 | Oncogene | In vitro: A549, H1299, Calu6,H520,95-D, PC9,HCC827 | SUMO promotes tumor growth of lysine residues K177, K211, K212 and K215 in NSCLC | Cisplatin/ Gefitinib | |
WTAP | Oncogene | In vitro: H1299, A549, EBC-1, HCC827,CALU-3, H661,H596, H358, H460,H1650, H1975, H1395,H292 | Down-regulation of c-MET expression | Crizotinib | [54] | |
YTHDF1 | Suppressor | In vitro: HEK-293T, H1975, A549, NCI-H838, H1299, NCI-H1650,GLC-82, SPC-A1 | regulating the translational efficiency of CDK2, CDK4, and cyclin D1 | Cisplatin | [55] | |
Hepatocellular cance | METTL3 | Oncogene | In vitro: HepG2,Huh-7,MHCC97L, HepG-2,Hepa1-6, HEK-293T,WRL68, HUVEC,SMMC-7721, Bel7402,HepG-2, WRL68, HEK-293T | Reduce the stability of SOCS2 mRNA | Sorafenib | |
METTL14 | Oncogene | In vivo: mice | Progress in regulating miR-126 through DGCR8 | Sorafenib | [58] | |
YTHDF2 | Oncogene | In vitro: HepG2,293T | MiR-145 regulates m6A level by targeting YTHDF2 mRNA 3-UTR in hepatocellular carcinoma cells | – | [59] | |
Gastric cancer | METTL3 | Suppressor | In vitro: AGS,HGC-27, MKN-45 | mediated this process occurred on the A879 locus of pri-miR-17-92 | Everolimus | [60] |
Colorectal cancer | YTHDF1 | Oncogene | In vitro: SW480,CaCO2, HT29, RKO,DLD-1, KM12SM, HCT-116,LoVo | C-Myc promotes the expression of YTHDF1 and affects the proliferation and chemosensitivity of colorectal cancer | Oxaliplatin/ 5-Fu | [61] |
Pancreatic cancer | METTL3 | Oncogene | In vitro: MIA PaCa-2 | METTL3 is associated with mitogen-activated protein kinase cascades, ubiquitin-dependent process and RNA splicing and regulation of cellular process | Cisplatin/ Fu / Y-Irradiation | [62] |