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乙型肝炎病毒 X 基因(HBx)整合通过 HBx/Alu 核心序列/端粒下 DNA 的重组参与肝癌发生。

Involvement of hepatitis B virus X gene (HBx) integration in hepatocarcinogenesis via a recombination of HBx/Alu core sequence/subtelomeric DNA.

机构信息

Department of Cancer Research, Key Laboratory of Molecular Microbiology and Technology of Ministry of Education, College of Life Sciences, Nankai University, PR China.

出版信息

FEBS Lett. 2012 Sep 21;586(19):3215-21. doi: 10.1016/j.febslet.2012.06.039. Epub 2012 Jul 3.

DOI:10.1016/j.febslet.2012.06.039
PMID:22771476
Abstract

The significance of hepatitis B virus (HBV) DNA-based integration in hepatocarcinogenesis is poorly understood. In the present study, we investigated whether the integration of HBV X gene (HBx) is involved in the event. Our finding showed that the integration of HBx fragment (316-462 bp/262-462 bp) was able to transform human immortalized normal liver LO2 cells using a cell model of HBx-integration. We identified that the recombination, HBx/Alu core sequence/subtelomeric DNA, was required for the transformation, which could be detected in 5 out of 44 clinical HBx-positive hepatocellular carcinoma tissues. Thus, we conclude that HBx integration is involved in the hepatocarcinogenesis.

摘要

乙型肝炎病毒 (HBV) DNA 整合在肝癌发生中的意义尚未完全明确。本研究旨在探讨 HBV X 基因 (HBx) 的整合是否参与了这一事件。我们的研究结果表明,使用 HBx 整合细胞模型,能够将 HBx 片段(316-462bp/262-462bp)整合到永生化正常人类肝脏 LO2 细胞中,导致其转化。我们鉴定出重组、HBx/Alu 核心序列/端粒外 DNA 是转化所必需的,在 44 例 HBx 阳性肝细胞癌组织中有 5 例可检测到这种重组。因此,我们得出结论,HBx 整合参与了肝癌的发生。

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