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Splicing factor SRSF1 promotes breast cancer progression via oncogenic splice switching of PTPMT1

机译:拼接因子SRSF1通过PTPMT1的致癌剪接切换促进乳腺癌进展

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Intensive evidence has highlighted the effect of aberrant alternative splicing (AS) events on cancer progression when triggered by dysregulation of the SR protein family. Nonetheless, the underlying mechanism in breast cancer (BRCA) remains elusive. Here we sought to explore the molecular function of SRSF1 and identify the key AS events regulated by SRSF1 in BRCA. We conducted a comprehensive analysis of the expression and clinical correlation of SRSF1 in BRCA based on the TCGA dataset, Metabric database and clinical tissue samples. Functional analysis of SRSF1 in BRCA was conducted in vitro and in vivo. SRSF1-mediated AS events and their binding motifs were identified by RNA-seq, RNA immunoprecipitation-PCR (RIP-PCR) and in vivo crosslinking followed by immunoprecipitation (CLIP), which was further validated by the minigene reporter assay. PTPMT1 exon 3 (E3) AS was identified to partially mediate the oncogenic role of SRSF1 by the P-AKT/C-MYC axis. Finally, the expression and clinical significance of these AS events were validated in clinical samples and using the TCGA database. SRSF1 expression was consistently upregulated in BRCA samples, positively associated with tumor grade and the Ki-67 index, and correlated with poor prognosis in a hormone receptor-positive (HR ) cohort, which facilitated proliferation, cell migration and inhibited apoptosis in vitro and in vivo. We identified SRSF1-mediated AS events and discovered the SRSF1 binding motif in the regulation of splice switching of PTPMT1. Furthermore, PTPMT1 splice switching was regulated by SRSF1 by binding directly to its motif in E3 which partially mediated the oncogenic role of SRSF1 by the AKT/C-MYC axis. Additionally, PTPMT1 splice switching was validated in tissue samples of BRCA patients and using the TCGA database. The high-risk group, identified by AS of PTPMT1 and expression of SRSF1, possessed poorer prognosis in the stage I/II TCGA BRCA cohort. SRSF1 exerts oncogenic roles in BRCA partially by regulating the AS of PTPMT1, which could be a therapeutic target candidate in BRCA and a prognostic factor in HR BRCA patient.
机译:在SR蛋白家族的失调触发时,强化证据强调了异常替代剪接(AS)事件对癌症进展的影响。尽管如此,乳腺癌(BRCA)的潜在机制仍然难以捉摸。在这里,我们寻求探索SRSF1的分子功能,并将关键视为BRCA中SRSF1调控的事件。我们对基于TCGA数据集,元数据库和临床组织样本的BRCA中SRSF1的表达和临床相关性进行了全面分析。在体外和体内进行BRCA的SRSF1的功能分析。通过RNA-SEQ,RNA免疫沉淀-PCR(RIP-PCR)和体内交联鉴定SRSF1介导的事件及其结合基质,然后通过MINIGENE报告分析进一步验证的免疫沉淀(夹子)。鉴定为PTPMT1外显子3(E3),以部分地介导SRSF1通过P-AKT / C-MYC轴的致癌作用。最后,在临床样本中验证了这些作为事件的表达和临床意义,并使用TCGA数据库验证。 SRSF1表达在BRCA样品中持续上调,与肿瘤级和KI-67指数正相关,并与激素受体阳性(HR)队列的预后差相关,促进增殖,细胞迁移和体外抑制细胞凋亡体内。我们将SRSF1介导的事件鉴定为事件,并在PTPMT1的接头切换的调节中发现了SRSF1结合基序。此外,通过直接将SRSF1直接与E3中的基序结合来调节PTPMT1接头切换,其部分地介导SRSF1通过Akt / C-Myc轴的致癌作用。此外,PTPMT1剪接切换在BRCA患者的组织样本中验证并使用TCGA数据库。通过PTPMT1鉴定的高风险组和SRSF1的表达,在I / II型TCGA BRCA队列中具有较差的预后。 SRSF1部分通过调节PTPMT1的AS施用BRCA的致癌作用,这可以是BRCA中的治疗目标候选者和HR BRCA患者的预后因子。

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