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本文引用的文献

1
Hepatitis B virus X protein represses miRNA-148a to enhance tumorigenesis.乙型肝炎病毒 X 蛋白抑制 microRNA-148a 以增强肿瘤发生。
J Clin Invest. 2013 Feb;123(2):630-45. doi: 10.1172/JCI64265. Epub 2013 Jan 16.
2
miR-101 is down-regulated by the hepatitis B virus x protein and induces aberrant DNA methylation by targeting DNA methyltransferase 3A.miR-101 受乙型肝炎病毒 x 蛋白下调,并通过靶向 DNA 甲基转移酶 3A 诱导异常的 DNA 甲基化。
Cell Signal. 2013 Feb;25(2):439-46. doi: 10.1016/j.cellsig.2012.10.013. Epub 2012 Nov 1.
3
Role of miR-148a in hepatitis B associated hepatocellular carcinoma.miR-148a 在乙型肝炎相关肝细胞癌中的作用。
PLoS One. 2012;7(4):e35331. doi: 10.1371/journal.pone.0035331. Epub 2012 Apr 9.
4
Histone H3 lysine 56 methylation regulates DNA replication through its interaction with PCNA.组蛋白 H3 赖氨酸 56 甲基化通过与 PCNA 的相互作用调节 DNA 复制。
Mol Cell. 2012 Apr 13;46(1):7-17. doi: 10.1016/j.molcel.2012.01.019. Epub 2012 Mar 1.
5
Role of epigenetic aberrations in the development and progression of human hepatocellular carcinoma.表观遗传异常在人类肝细胞癌发生发展中的作用。
Cancer Lett. 2014 Jan 28;342(2):223-30. doi: 10.1016/j.canlet.2012.01.038. Epub 2012 Feb 2.
6
Inhibition of PP1 phosphatase activity by HBx: a mechanism for the activation of hepatitis B virus transcription.HBx 抑制 PP1 磷酸酶活性:乙型肝炎病毒转录激活的一种机制。
Sci Signal. 2012 Jan 3;5(205):ra1. doi: 10.1126/scisignal.2001906.
7
DNA methylation: superior or subordinate in the epigenetic hierarchy?DNA甲基化:在表观遗传层级中是处于上位还是下位?
Genes Cancer. 2011 Jun;2(6):607-17. doi: 10.1177/1947601910393957.
8
Epigenetic repression of E-cadherin expression by hepatitis B virus x antigen in liver cancer.乙型肝炎病毒 x 抗原在肝癌中通过表观遗传抑制 E-钙黏蛋白的表达。
Oncogene. 2012 Feb 2;31(5):563-72. doi: 10.1038/onc.2011.255. Epub 2011 Jun 27.
9
Hepatitis B virus X protein activates CD59 involving DNA binding and let-7i in protection of hepatoma and hepatic cells from complement attack.乙型肝炎病毒 X 蛋白通过 DNA 结合和 let-7i 激活 CD59,从而保护肝癌和肝细胞免受补体攻击。
Carcinogenesis. 2011 Aug;32(8):1190-7. doi: 10.1093/carcin/bgr106. Epub 2011 Jun 10.
10
Hepatitis B virus X gene and hepatocarcinogenesis.乙型肝炎病毒 X 基因与肝癌发生。
J Gastroenterol. 2011 Aug;46(8):974-90. doi: 10.1007/s00535-011-0415-9. Epub 2011 Jun 8.

乙型肝炎病毒 X 蛋白诱导的异常表观遗传修饰导致人类肝细胞癌的发病机制。

Hepatitis B virus X protein-induced aberrant epigenetic modifications contributing to human hepatocellular carcinoma pathogenesis.

机构信息

Institute of Immunology, PLA, Third Military Medical University, Chongqing, People's Republic of China.

出版信息

Mol Cell Biol. 2013 Aug;33(15):2810-6. doi: 10.1128/MCB.00205-13. Epub 2013 May 28.

DOI:10.1128/MCB.00205-13
PMID:23716588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3719687/
Abstract

Hepatocellular carcinoma (HCC) remains one of the most prevalent malignant diseases worldwide, and the majority of cases are related to hepatitis B virus (HBV) infection. Interactions between the HBV-encoded X (HBx) protein and host factors are known to play major roles in the onset and progression of HBV-related HCC. These dynamic molecular mechanisms are extremely complex and lead to prominent changes in the host genetic and epigenetic architecture. This review summarizes the current knowledge about HBx-induced epigenetic changes, including aberrations in DNA methylation, histone modifications, and microRNA expression, and their roles in HBV-infected liver cells and HBV-related HCC. Moreover, the HBx-mediated epigenetic control of HBV covalently closed circular DNA (cccDNA) is also discussed. Although this field of study is relatively new, the accumulated evidence has indicated that the epigenetic events induced by HBx play important roles in the development of HBV-related HCC. Ongoing research will help to identify practical applications of the HBV-related epigenetic signatures as biomarkers for early HCC detection or as potential targets to prevent and treat HBV-related HCC.

摘要

肝细胞癌 (HCC) 仍然是全球最常见的恶性疾病之一,大多数病例与乙型肝炎病毒 (HBV) 感染有关。已知乙型肝炎病毒编码 X (HBx) 蛋白与宿主因子之间的相互作用在乙型肝炎病毒相关 HCC 的发病和进展中起主要作用。这些动态的分子机制非常复杂,导致宿主遗传和表观遗传结构的显著变化。本综述总结了目前关于 HBx 诱导的表观遗传变化的知识,包括 DNA 甲基化、组蛋白修饰和 microRNA 表达的异常,以及它们在 HBV 感染的肝细胞和 HBV 相关 HCC 中的作用。此外,还讨论了 HBx 介导的 HBV 共价闭合环状 DNA (cccDNA) 的表观遗传调控。尽管这一研究领域相对较新,但积累的证据表明,HBx 诱导的表观遗传事件在乙型肝炎病毒相关 HCC 的发展中起重要作用。正在进行的研究将有助于确定 HBV 相关表观遗传特征作为早期 HCC 检测的生物标志物或预防和治疗 HBV 相关 HCC 的潜在靶点的实际应用。