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NSUN2通过介导ARMC9的m5C修饰促进胃癌细胞的增殖、转移和侵袭

NSUN2 promotes proliferation, migration, and invasion of gastric cancer cells by mediating m5C modification of ARMC9

  • 摘要: 为研究NOP2/Sun RNA甲基转移酶2(NOP2/Sun RNA methyltransferase 2,NSUN2)对胃癌恶性进展的影响及其潜在机制,使用TCGA数据库分析发现胃癌组织中NSUN2表达水平显著升高;Western blot发现,与胃黏膜上皮细胞相比,NSUN2在胃癌细胞中表达上调;集落形成实验显示,NSUN2过表达细胞中集落形成能力增高;Transwell实验也证实NSUN2高表达时,发生迁移和侵袭的细胞数量显著增多。进一步通过数据库分析推测ARMC可能是NSUN2的下游靶分子,接着通过MeRIP-qPCR揭示NSUN2高表达可以提高ARMC9的m5C修饰水平,并且降低ARMC9 mRNA的降解速率,从而提高其蛋白表达水平。此外,过表达ARMC9可以增强细胞的集落形成能力和迁移侵袭能力。上述结果显示,NSUN2可以通过提高ARMC9 mRNA的m5C修饰水平,提高其稳定性,增强其表达,从而促进胃癌进展,因此NSUN2和ARMC9可以作为胃癌进展的潜在治疗靶标。

     

    Abstract: To investigate the impact and underlying mechanism of NOP2/Sun RNA methyltransferase 2 (NSUN2) on gastric cancer progression, TCGA database was used and revealed a significant upregulation of NSUN2 expression in gastric cancer tissues. Western blot analysis revealed that NSUN2 was upregulated in gastric cancer cells compared with gastric mucosal epithelial cells. Colony formation assays demonstrated an enhanced colony-forming capacity in NSUN2-overexpressing cells. Furthermore, Transwell assays showed a marked increase in cell migration and invasion upon high NSUN2 expression. Moreover, TCGA database analysis suggested ARMC9 as a potential downstream target of NSUN2. Subsequently, MeRIP-qPCR analysis revealed that NSUN2 overexpression could increase m5C modification of ARMC9 mRNA, and reduce its degradation rate, thus enhancing protein expression. Additionally, ARMC9 overexpression augmented cellular colony formation and migratory and invasive capabilities. These findings indicate that NSUN2 promotes gastric cancer progression by elevating m5C modification of ARMC9 mRNA, increasing its stability and enhancing its expression, therefore, NSUN2 and ARMC9 may serve as potential therapeutic targets for gastric cancer.

     

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