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Table 1 The role and mechanism of m6A regulators in OC

From: Roles of N6-methyladenosine (m6A) modifications in gynecologic cancers: mechanisms and therapeutic targeting

m6A regulators

Roles

Genes/RNAs

Mechanisms

Model

Refs.

Writers

METTL3

Oncogene

AXL

METTL3 stimulates AXL translation and EMT

In vitro; in vivo

[30]

METTL3

Oncogene

AKT

METTL3 regulates the phosphorylation levels of AKT and the expression of the downstream effector Cyclin D1

In vitro

[32]

METTL3

Oncogene

miR-126-5p

METTL3 promotes miR-126-5p maturation, leading to the activation of PTEN-mediated PI3K/Akt/mTOR pathway

In vitro; in vivo

[33]

METTL3

Oncogene

RHPN1-AS1

METTL3 increases m6A level of lncRNA RHPN1-AS1 and contributes to its stability

In vitro; in vivo

[37]

METTL14

Tumor suppressor

TROAP

METTL14 negatively regulates TROAP expression in an m6A-dependent manner

In vitro; in vivo

[40]

Readers

YTHDF1

Oncogene

TRIM29

YTHDF1 promotes TRIM29 translation, then affecting the CSC-like characteristics of OC cells

In vitro

[49]

YTHDF1

Oncogene

EIF3C

YTHDF1 promotes EIF3C’s translation in an m6A-dependent manner and affects the overall protein translation

In vitro; in vivo

[47]

YTHDF2

Oncogene

miR-145

A double negative feedback loop between miR-145 and YTHDF2, regulates the proliferation and migration of OC cells

In vitro

[48]

YTHDF2

Oncogene

FBW7

YTHDF2 is suppressed by FBW7, recognizes m6A-modifed BMF mRNA and accelerates decay of the latter

In vitro; in vivo

[45]

IGF2BP1

Oncogene

SRF

IGF2BP1 promotes SRF expression to augment SRF-dependent transcription

In vitro

[46]

IGF2BP1

Tumor suppressor

UBA6

IGF2BP1 enhances the stability of UBA6 mRNA, thus inhibiting the malignancy of OC

In vitro

[51]

Erasers

FTO

Tumor suppressor

PDE1C PDE4B

FTO reduces m6A level at the 3’UTR and the mRNA stability of PDE1C and PDE4B, thus blocking cAMP pathway

In vitro; In vivo

[53]

FTO

unknown

ATG5/7

circRAB11FIP1 promotes autophagy through FTO-mediated demethylation of ATG5 and ATG7

In vitro

[57]

Erasers

FTO/ALKBH5

unknown

FZD10

Downregulation of ALKBH5 and FTO contribute to PARPi resistance by increasing m6A modification in FZD10 mRNA to upregulate Wnt signaling

In vitro; in vivo

[56]

ALKBH5

Oncogene

NANOG

Highly expressed TLR4 activates NF-κB pathway, upregulates ALKBH5 expression and increases m6A level and NANOG expression

In vitro; in vivo

[54]

ALKBH5

Oncogene

JAK2

ALKBH5-HOXA10 loop jointly activates the JAK2/STAT3 signaling pathway by mediating JAK2 m6A demethylation

In vitro; in vivo

[55]

Immunoregulators

ZC3H13/YTHDF1/IGF2BP1

NA

NA

Important immune cell infiltration-regulated m6A regulators

NA

[79]

  1. NA not available