The METTL3 inhibitor STM2457 suppresses gastric cancer progression by modulating m6A RNA modification

H Hang Sun H Haozhi Xu J Junying Li X Xiaoman Xie J Junmei Zhang H Hongjie Dong H Huanhuan Xie Q Qi Wang G Guihua Zhao K Kun Yin J Jingyu Yang (Department of Pharmacology, School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University) J Jianwei Zhou R Ruili Wu C Chao Xu

Abstract

Gastric cancer (GC) is one of the most common and lethal cancers globally. methyltransferase-like 3 (METTL3)-mediated N6-methyladenosine (m 6 A) RNA methylation plays a crucial role in tumor initiation and progression by regulating RNA function. STM2457, a highly efficient METTL3 inhibitor, can inhibit METTL3 activity and may serve as a potential therapeutic strategy in cancers. However, the role of STM2457 for GC cells is still unknown. In this study, we analyzed the expression profile data of GC in TCGA and GEO databases, and further explored the expression involvement of METTL3 in GC cell line, investigated the therapeutic effect of STM2457 targeted inhibition of METTL3 in GC both in vitro and in vivo experiments. The results indicated that STM2457 could suppress GC cell proliferation and migration by inhibiting METTL3, and also promoted cell apoptosis and arrest the cell cycle in S phase. In addition, STM2457 could inhibit tumor growth in subcutaneous xenotransplantation mouse model. Our findings suggested that STM2457 had great potential for the treatment of GC and could serve as a foundation for future clinical applications.

Article Details

Journal PLoS ONE
Volume / Issue Vol. 21, Issue 3
Published March 24, 2026
Pages e0345744
ISSN 1932-6203
Publisher Public Library of Science

Journal Info

PLoS ONE

Public Library of Science

ISSN: 1932-6203 Open Access Health Sciences

Authors (14)

H

Hang Sun

H

Haozhi Xu

J

Junying Li

X

Xiaoman Xie

J

Junmei Zhang

H

Hongjie Dong

H

Huanhuan Xie

Q

Qi Wang

G

Guihua Zhao

K

Kun Yin

J

Jingyu Yang

Department of Pharmacology, School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University

J

Jianwei Zhou

R

Ruili Wu

C

Chao Xu