Sino-US Research Center for Cancer Translational Medicine of the Second Affiliated Hospital of Dalian Medical University & Institute of Cancer Stem Cell, Dalian Medical University, Dalian, 116023, China.
Department of Immunology, College of Basic Medical Sciences, Dalian Medical University, Dalian, 116044, China.
Sci China Life Sci. 2024 Oct;67(10):2186-2197. doi: 10.1007/s11427-023-2582-x. Epub 2024 Aug 2.
Increasing evidence suggests that deregulated RNA splicing factors play critical roles in tumorigenesis; however, their specific involvement in colon cancer remains largely unknown. Here we report that the splicing factor RBM25 is overexpressed in colon cancer, and this increased expression correlates with a poor prognosis of patients with colon cancer. Functionally, RBM25 ablation suppresses the growth of colon cancer cells both in vitro and in vivo. Mechanistically, our transcriptome-wide analysis of splicing events revealed that RBM25 regulates a large number of cancer-related alternative splicing events across the human genome in colon cancer. Particularly, RBM25 regulates the splicing of MNK2 by interacting with the poly G rich region in exon 14a, thereby inhibiting the selection of the proximal 3' splice site (ss), resulting in the production of the oncogenic short isoform, MNK2b. Knockdown of RBM25 leads to an increase in the MNK2a isoform and a decrease in the MNK2b isoform. Importantly, re-expression of MNK2b or blocking the 3' ss of the alternative exon 14a with ASO partially reverses the RBM25 knockdown mediated tumor suppression. Moreover, MNK2b levels were significantly increased in colon cancer tissues, which is positively correlated with the expression level of RBM25. Collectively, our findings uncover the critical role of RBM25 as a key splicing factor in colon cancer, suggesting its potential as a prognostic marker and therapeutic target.
越来越多的证据表明,RNA 剪接因子失调在肿瘤发生中发挥着关键作用;然而,它们在结肠癌中的具体作用在很大程度上仍不清楚。在这里,我们报告剪接因子 RBM25 在结肠癌中过表达,并且这种表达增加与结肠癌患者的预后不良相关。功能上,RBM25 的缺失抑制了结肠癌细胞在体外和体内的生长。在机制上,我们对剪接事件的全转录组分析表明,RBM25 在结肠癌中调节了大量与癌症相关的可变剪接事件。特别是,RBM25 通过与外显子 14a 中的富含 poly G 区域相互作用来调节 MNK2 的剪接,从而抑制近端 3' 剪接位点(ss)的选择,导致致癌的短异构体 MNK2b 的产生。RBM25 的敲低导致 MNK2a 异构体的增加和 MNK2b 异构体的减少。重要的是,MNK2b 的重新表达或用 ASO 阻断替代外显子 14a 的 3' ss 部分逆转了 RBM25 敲低介导的肿瘤抑制。此外,MNK2b 水平在结肠癌组织中显著增加,与 RBM25 的表达水平呈正相关。总之,我们的研究结果揭示了 RBM25 作为结肠癌关键剪接因子的关键作用,表明其作为预后标志物和治疗靶点的潜力。