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多嘧啶序列结合蛋白1通过调节丙酮酸激酶M2的可变剪接促进透明细胞肾细胞癌的增殖、迁移和侵袭。

Polypyrimidine Tract-Binding Protein 1 promotes proliferation, migration and invasion in clear-cell renal cell carcinoma by regulating alternative splicing of PKM.

作者信息

Jiang Junyi, Chen Xu, Liu Hao, Shao Jing, Xie Ruihui, Gu Peng, Duan Chaohui

机构信息

Department of Laboratory Medicine, Sun Yat-sen Memorial Hospital, Sun Yat-sen UniversityGuangzhou, China; Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen UniversityGuangzhou, China.

Department of Urology, Sun Yat-sen Memorial Hospital, Sun Yat-sen UniversityGuangzhou, China; Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Sun Yat-sen UniversityGuangzhou, China.

出版信息

Am J Cancer Res. 2017 Feb 1;7(2):245-259. eCollection 2017.

Abstract

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 . 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 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.

摘要

多嘧啶序列结合蛋白1(PTBP1)是一种重要的RNA结合蛋白,通过调控mRNA的可变剪接来调节多种生物学事件。PTBP1可诱导促进癌症发生的剪接变体,并且与多种癌症的肿瘤发生相关。然而,PTBP1在透明细胞肾细胞癌(ccRCC)中的表达模式和生物学机制尚不清楚。我们通过免疫组织化学检测了来自TCGA的533例ccRCC患者和30例ccRCC患者中PTBP1的表达,发现PTBP1在ccRCC组织中的表达水平显著升高,并且PTBP1高表达与肿瘤晚期、AJCC分期及预后不良密切相关。利用小干扰RNA介导的敲低和慢病毒载体介导的过表达进行的细胞生物学实验表明,PTBP1可促进ccRCC细胞的增殖、迁移和侵袭。此外,PTBP1增加了丙酮酸激酶M1(PKM1)向PKM2的转变。敲低PKM2主要消除了PTBP1诱导的ccRCC细胞增殖、迁移和侵袭。总之,我们的研究表明,PTBP1通过介导PKM2的可变剪接在ccRCC中发挥致瘤作用,它可能是一种潜在的预后标志物和ccRCC治疗的有前景的靶点。

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