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首页> 外文期刊>Biochemical and Biophysical Research Communications >RBP-J-interacting and tubulin-associated protein induces apoptosis and cell cycle arrest in human hepatocellular carcinoma by activating the p53-Fbxw7 pathway
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RBP-J-interacting and tubulin-associated protein induces apoptosis and cell cycle arrest in human hepatocellular carcinoma by activating the p53-Fbxw7 pathway

机译:RBP-J相互作用和微管蛋白相关蛋白通过激活p53-Fbxw7途径诱导人肝癌细胞凋亡和细胞周期停滞

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摘要

Aberrant Notch signaling is observed in human hepatocellular carcinoma (HCC) and has been associated with the modulation of cell growth. However, the role of Notch signaling in HCC and its underlying mechanism remain elusive. RBP-J-interacting and tubulin-associated (RITA) mediates the nuclear export of RBP-J to tubulin fibers and downregulates Notch-mediated transcription. In this study, we found that RITA overexpression increased protein expression of p53 and Fbxw7 and downregulated the expression of cyclin D1, cyclin E, CDK2, Hes-1 and NF-kappa B p65. These changes led to growth inhibition and induced G0/G1 cell cycle arrest and apoptosis in SMMC7721 and HepG2 cells. Our findings indicate that RITA exerts tumor-suppressive effects in hepatocarcinogenesis through induction of G0/G1 cell cycle arrest and apoptosis and suggest a therapeutic application of RITA in HCC. (C) 2014 Elsevier Inc. All rights reserved.
机译:在人类肝细胞癌(HCC)中观察到异常的Notch信号传导,并且与细胞生长的调节有关。但是,Notch信号在肝癌中的作用及其潜在机制仍然难以捉摸。 RBP-J相互作用和微管蛋白相关(RITA)介导RBP-J的核输出到微管蛋白纤维,并下调Notch介导的转录。在这项研究中,我们发现RITA过表达会增加p53和Fbxw7的蛋白表达,并下调cyclin D1,cyclin E,CDK2,Hes-1和NF-κB p65的表达。这些变化导致SMMC7721和HepG2细胞生长受到抑制,并诱导G0 / G1细胞周期停滞和凋亡。我们的发现表明,RITA通过诱导G0 / G1细胞周期停滞和凋亡而在肝癌发生中发挥肿瘤抑制作用,并提示RITA在肝癌中的治疗应用。 (C)2014 Elsevier Inc.保留所有权利。

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