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丙型肝炎病毒NS5A蛋白的过表达通过有丝分裂细胞周期失调诱导染色体不稳定。

Overexpression of hepatitis C virus NS5A protein induces chromosome instability via mitotic cell cycle dysregulation.

作者信息

Baek Kwan-Hyuck, Park Hye-Young, Kang Chang-Mo, Kim So-Jung, Jeong Sook-Jung, Hong Eun-Kyung, Park Joong-Won, Sung Young-Chul, Suzuki Tetsuro, Kim Chang-Min, Lee Chang-Woo

机构信息

Research Institute, National Cancer Center, Goyang, South Korea.

出版信息

J Mol Biol. 2006 May 26;359(1):22-34. doi: 10.1016/j.jmb.2006.03.020. Epub 2006 Mar 29.

Abstract

Hepatocellular carcinoma (HCC) is a common primary cancer associated with high incidences of genetic variations including chromosome instability. Moreover, it has been demonstrated that hepatitis C virus (HCV) is one of the major causes of HCC. However, no previous work has assessed whether HCV proteins are associated with the induction of chromosome instability. Here, we found that liver cell lines constitutively expressing full-length or truncated versions of the HCV genome show a high incidence of chromosome instability. In particular, the overexpression of HCV NS5A protein in cultured liver cells was found to promote chromosome instability and aneuploidy. Further experiments showed that NS5A-induced chromosome instability is associated with aberrant mitotic regulations, such as, an unscheduled delay in mitotic exit and other mitotic impairments (e.g. multi-polar spindles). Thus, our results indicate that HCV NS5A protein may be directly involved in the induction of chromosome instability via mitotic cell cycle dysregulation, and provide novel insights into the molecular mechanisms of HCV-associated hepatocarcinogenesis.

摘要

肝细胞癌(HCC)是一种常见的原发性癌症,与包括染色体不稳定性在内的高频率基因变异有关。此外,已有研究表明丙型肝炎病毒(HCV)是HCC的主要病因之一。然而,此前尚无研究评估HCV蛋白是否与染色体不稳定性的诱导有关。在此,我们发现持续表达HCV基因组全长或截短版本的肝细胞系显示出高频率的染色体不稳定性。特别是,在培养的肝细胞中,HCV NS5A蛋白的过表达被发现会促进染色体不稳定性和非整倍体形成。进一步的实验表明,NS5A诱导的染色体不稳定性与异常的有丝分裂调控有关,例如有丝分裂退出的意外延迟和其他有丝分裂缺陷(如多极纺锤体)。因此,我们的结果表明,HCV NS5A蛋白可能通过有丝分裂细胞周期失调直接参与染色体不稳定性的诱导,并为HCV相关肝癌发生发展的分子机制提供了新的见解。

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