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首页> 外文期刊>American Journal of Cancer Research >Polypyrimidine Tract-Binding Protein 1 promotes proliferation, migration and invasion in clear-cell renal cell carcinoma by regulating alternative splicing of PKM
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Polypyrimidine Tract-Binding Protein 1 promotes proliferation, migration and invasion in clear-cell renal cell carcinoma by regulating alternative splicing of PKM

机译:聚嘧啶束缚结合蛋白1通过调节PKM的可变剪接促进透明细胞肾细胞癌的增殖,迁移和侵袭

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摘要

Polypyrimidine Tract-Binding Protein 1 (PTBP1) is an essential RNA-binding protein that regulates diverse biological events through regulating alternative splice of mRNA. PTBP1 induces cancer-promoting splice variants and is related to tumorigenesis in several cancers. However, both the expression patterns and biological mechanisms of PTBP1 in clear-cell renal cell carcinoma (ccRCC) are unclear. We investigated PTBP1 expression in 533 ccRCC patients from TCGA and 30 ccRCC patients by immunohistochemistry, and found that PTBP1 expression levels were significantly increased in ccRCC tissues and that high PTBP1 expression was closely correlated with advanced tumor stage, AJCC stage and poor prognosis. Cell biological assays with siRNA-mediated knockdown and lentivirus vector-mediated over-expression demonstrated that PTBP1 promoted proliferation, migration and invasion in ccRCC cells in vitro. Furthermore, PTBP1 increased the transformation from pyruvate kinase muscle 1 (PKM1) to PKM2. Knockdown of PKM2 mainly abolished PTBP1-induced proliferation, migration and invasion in ccRCC cells in vitro. In conclusion, our study indicates that PTBP1 plays a tumorigenic role in ccRCC by mediating PKM2 alternative splicing and it may be a potential prognostic marker and a promising target for treatment of ccRCC.
机译:聚嘧啶区结合蛋白1(PTBP1)是一种必需的RNA结合蛋白,可通过调节mRNA的可变剪接来调节多种生物学事件。 PTBP1诱导促进癌症的剪接变体,并与几种癌症的肿瘤发生有关。但是,尚不清楚PTBP1在透明细胞肾细胞癌(ccRCC)中的表达模式和生物学机制。我们通过免疫组织化学研究了533 TCGA和30 ccRCC ccRCC患者中PTBP1的表达,发现PTBP1表达在ccRCC组织中显着增加,并且PTBP1高表达与晚期肿瘤,AJCC阶段和不良预后密切相关。 siRNA介导的基因敲除和慢病毒载体介导的过表达的细胞生物学分析表明,PTBP1在体外促进ccRCC细胞的增殖,迁移和侵袭。此外,PTBP1增加了从丙酮酸激酶肌肉1(PKM1)到PKM2的转化。敲除PKM2主要消除了PTBP1诱导的ccRCC细胞在体外的增殖,迁移和侵袭。总之,我们的研究表明PTBP1通过介导PKM2选择性剪接在ccRCC中发挥致癌作用,它可能是潜在的预后标志物和有希望的ccRCC治疗靶标。

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