Lu Qiutong, Wang Zhaopeng, Cao Shuixian, Wang Huan, Li Nianshuang, Hu Yi, Ding Wuhui, Zuo Wei, Hong Junbo
Department of Gastroenterology, Jiangxi Provincial Key Laboratory of Digestive Diseases, Jiangxi Clinical Research Center for Gastroenterology, Digestive Disease Hospital, The First Affiliated Hospital, Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, PR China.
Department of Gastroenterology, Guixi People's Hospital Guixi, Yingtan, Jiangxi, PR China.
Cell Death Dis. 2025 Aug 18;16(1):625. doi: 10.1038/s41419-025-07841-4.
Helicobacter pylori (H. pylori) infection is a significant cause of gastric diseases, with its pathogenic mechanisms still not fully understood. This study investigates the role of METTL3, an enzyme involved in m6A methylation, in modulating the CXCL1/NF-κB signaling pathway in H. pylori-induced gastritis. Using both bioinformatics analysis of GEO database and experimental approaches including MeRIP, RIP assays, and immunostaining, this research highlights how METTL3 influences CXCL1 expression and NF-κB pathway activation. Results from both in vitro and in vivo models show that METTL3 increases inflammatory responses and apoptosis in gastric cells. Suppression of METTL3 resulted in decreased inflammation and apoptosis, suggesting its potential as a therapeutic target in gastritis management.
幽门螺杆菌(H. pylori)感染是胃部疾病的一个重要病因,其致病机制仍未完全明确。本研究调查了参与m6A甲基化的酶METTL3在调节幽门螺杆菌诱导的胃炎中CXCL1/NF-κB信号通路中的作用。通过对GEO数据库进行生物信息学分析以及采用包括MeRIP、RIP分析和免疫染色在内的实验方法,本研究突出了METTL3如何影响CXCL1表达和NF-κB通路激活。体外和体内模型的结果均表明,METTL3会增加胃细胞中的炎症反应和细胞凋亡。抑制METTL3会导致炎症和细胞凋亡减少,这表明它在胃炎治疗中具有作为治疗靶点的潜力。