Shen Xudong, Zhao Kui, Xu Liming, Cheng Guilian, Zhu Jianhong, Gan Lei, Wu Yongyou, Zhuang Zhixiang
Department of Oncology, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Department of General Surgery, The Second Affiliated Hospital of Soochow University, Suzhou, China.
Front Genet. 2021 Jan 11;11:592042. doi: 10.3389/fgene.2020.592042. eCollection 2020.
Gastric cancer (GC) is one of the most common malignancies in the world, and the fourth most frequent malignancy worldwide. YTHDF2 (YTH domain family 2, YTHDF2) binds to mRNA containing m6A, thereby regulating the localization and stability of the bound mRNA. YTHDF2 was shown to be associated with some cancer patient prognosis. However, the effect of YTHDF2 on gastric cancer and the molecular mechanism of this effect have not been documented.
To conduct this research, YTHDF2 expression levels in public databases and gastric cancer patient samples were analyzed. The effects of YTHDF2 on the growth of gastric cancer cells were detected and RNA-seq was used to analyze the signal pathways regulated by YTHDF2, and experiments were carried out for verification.
In our study, we found that YTHDF2 has lower expression in GC tissues and GC cells, and inhibits the growth of GC cells. In addition, the analysis of clinical data found that the expression level of YTHDF2 is closely related to the stage of GC and the survival of patients with GC. RNA sequencing results showed that overexpression of YTHDF2 significantly reduced protein expression in the FOXC2 (Forkhead box protein C2, FOXC2) signaling pathway. Finally, we found that knockout of FOXC2 reversed the inhibitory effect of YTHDF2 on GC cells.
In summary, YTHDF2 inhibits the growth of GC cells by negatively regulating FOXC2 and may serve as a prognostic marker in GC.
胃癌(GC)是世界上最常见的恶性肿瘤之一,在全球最常见的恶性肿瘤中排名第四。YTHDF2(YTH结构域家族2)与含有m6A的mRNA结合,从而调节结合的mRNA的定位和稳定性。YTHDF2已被证明与一些癌症患者的预后相关。然而,YTHDF2对胃癌的影响及其作用的分子机制尚未见报道。
为开展本研究,分析了公共数据库和胃癌患者样本中YTHDF2的表达水平。检测了YTHDF2对胃癌细胞生长的影响,并利用RNA测序分析了YTHDF2调控的信号通路,并进行了实验验证。
在我们的研究中,我们发现YTHDF2在GC组织和GC细胞中表达较低,并抑制GC细胞的生长。此外,临床数据分析发现,YTHDF2的表达水平与GC的分期和GC患者的生存密切相关。RNA测序结果表明,YTHDF2的过表达显著降低了FOXC2(叉头框蛋白C2)信号通路中的蛋白表达。最后,我们发现敲除FOXC2可逆转YTHDF2对GC细胞的抑制作用。
综上所述,YTHDF2通过负向调节FOXC2抑制GC细胞的生长,并可能作为GC的预后标志物。