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PcG相关蛋白RYBP在肝细胞癌中的表达及临床意义

Expression and clinical significance of PcG-associated protein RYBP in hepatocellular carcinoma.

作者信息

Zhu Xiaonian, Yan Meng, Luo Wei, Liu Wei, Ren Yuan, Bei Chunhua, Tang Guifang, Chen Ruiling, Tan Shengkui

机构信息

Department of Epidemiology and Statistics, School of Public Health, Guilin Medical University, Guilin, Guangxi 541000, P.R. China.

Department of Hepatobiliary Surgery, The Affiliated Hospital of Guilin Medical University, Guilin, Guangxi 541000, P.R. China; Department of General Surgery, First Central Hospital of Baoding, Baoding, Hebei 071000, P.R. China.

出版信息

Oncol Lett. 2017 Jan;13(1):141-150. doi: 10.3892/ol.2016.5380. Epub 2016 Nov 11.

Abstract

Ring1 and YY1 binding protein (RYBP), a member of the polycomb group proteins, has been implicated in transcription repression and tumor cell-specific apoptosis. Previously, RYBP has been reported as a putative tumor suppressor in cancer tissues by regulating mouse double minute 2 homolog-p53 signaling. However, the exact role and underlying mechanisms of RYBP in cancer remain to be fully elucidated. The present study investigated the expression profile of RYBP in hepatocellular carcinoma (HCC) and examined the association between the expression of RYBP and metastasis of HCC. It was found that RYBP was downregulated in HCC tissues, compared with matched adjacent non-tumor tissues, as detected by reverse transcription-quantitative polymerase chain reaction and immunohistochemistry. In addition, Kaplan-Meier survival analysis showed that the negative expression of RYBP was associated with decreased overall survival rates in patients with HCC. It was also found that RYBP was associated with zinc finger E-box binding homeobox 1 and zinc finger E-box binding homeobox 2, which were overexpressed in HCC and correlated with epithelial-mesenchymal transition. The results of the present study suggested the importance of RYBP in HCC and its possible mechanism in the metastasis of HCC.

摘要

环指蛋白1与YY1结合蛋白(RYBP)是多梳蛋白家族的成员之一,与转录抑制和肿瘤细胞特异性凋亡有关。此前,有报道称RYBP通过调节小鼠双微体2同源蛋白-p53信号通路,在癌组织中作为一种潜在的肿瘤抑制因子。然而,RYBP在癌症中的具体作用和潜在机制仍有待充分阐明。本研究调查了RYBP在肝细胞癌(HCC)中的表达谱,并检测了RYBP表达与HCC转移之间的关联。通过逆转录-定量聚合酶链反应和免疫组织化学检测发现,与配对的相邻非肿瘤组织相比,RYBP在HCC组织中表达下调。此外,Kaplan-Meier生存分析表明,RYBP的阴性表达与HCC患者总生存率降低相关。研究还发现,RYBP与锌指E盒结合同源框1和锌指E盒结合同源框2有关,这两种蛋白在HCC中过表达并与上皮-间质转化相关。本研究结果提示了RYBP在HCC中的重要性及其在HCC转移中的可能机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f2de/5244986/0afd2999414d/ol-13-01-0141-g00.jpg

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