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本文引用的文献

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Proliferation of primary human hepatocytes and prevention of hepatitis B virus reinfection efficiently deplete nuclear cccDNA in vivo.原代人肝细胞的增殖和乙型肝炎病毒再感染的有效预防可在体内有效耗尽核cccDNA。
Gut. 2018 Mar;67(3):542-552. doi: 10.1136/gutjnl-2016-312162. Epub 2017 Apr 20.
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The cancer epigenome: Concepts, challenges, and therapeutic opportunities.癌症表观基因组:概念、挑战与治疗机遇。
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PRMT5 restricts hepatitis B virus replication through epigenetic repression of covalently closed circular DNA transcription and interference with pregenomic RNA encapsidation.PRMT5 通过对共价闭合环状 DNA 转录的表观遗传抑制和对前基因组 RNA 衣壳形成的干扰来限制乙型肝炎病毒复制。
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Hepatitis B Reactivation Associated With Immune Suppressive and Biological Modifier Therapies: Current Concepts, Management Strategies, and Future Directions.与免疫抑制及生物调节剂治疗相关的乙型肝炎再激活:当前概念、管理策略及未来方向
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Hepatitis B virus X protein crosses out Smc5/6 complex to maintain covalently closed circular DNA transcription.乙型肝炎病毒X蛋白破坏Smc5/6复合物以维持共价闭合环状DNA转录。
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Hepatitis B Virus X Protein Promotes Degradation of SMC5/6 to Enhance HBV Replication.乙型肝炎病毒X蛋白促进SMC5/6降解以增强乙肝病毒复制。
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The molecular hallmarks of epigenetic control.表观遗传控制的分子特征。
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Establishment of an inducible HBV stable cell line that expresses cccDNA-dependent epitope-tagged HBeAg for screening of cccDNA modulators.建立一种可诱导的乙肝病毒(HBV)稳定细胞系,该细胞系表达依赖共价闭合环状DNA(cccDNA)的表位标签化HBeAg,用于筛选cccDNA调节剂。
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9
Histone H3 globular domain acetylation identifies a new class of enhancers.组蛋白H3球状结构域乙酰化鉴定出一类新的增强子。
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Combining Epigenetic and Immunotherapy to Combat Cancer.结合表观遗传学和免疫疗法对抗癌症。
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乙型肝炎病毒共价闭合环状DNA的表观遗传调控:对慢性乙型肝炎表观遗传治疗的意义

Epigenetic regulation of hepatitis B virus covalently closed circular DNA: Implications for epigenetic therapy against chronic hepatitis B.

作者信息

Hong Xupeng, Kim Elena S, Guo Haitao

机构信息

Department of Microbiology and Immunology, Georgetown University Medical Center, Washington, DC.

Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN.

出版信息

Hepatology. 2017 Dec;66(6):2066-2077. doi: 10.1002/hep.29479. Epub 2017 Nov 6.

DOI:10.1002/hep.29479
PMID:28833361
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5696023/
Abstract

Hepatitis B virus (HBV) infection represents a significant public health burden worldwide. Although current therapeutics manage to control the disease progression, lifelong treatment and surveillance are required because drug resistance develops during treatment and reactivations frequently occur following medication cessation. Thus, the occurrence of hepatocellular carcinoma is decreased, but not eliminated. One major reason for failure of HBV treatment is the inability to eradicate or inactivate the viral covalently closed circular DNA (cccDNA), which is a stable episomal form of the viral genome decorated with host histones and nonhistone proteins. Accumulating evidence suggests that epigenetic modifications of cccDNA contribute to viral replication and the outcome of chronic HBV infection. Here, we summarize current progress on HBV epigenetics research and the therapeutic implications for chronic HBV infection by learning from the epigenetic therapies for cancer and other viral diseases, which may open a new venue to cure chronic hepatitis B. (Hepatology 2017;66:2066-2077).

摘要

乙型肝炎病毒(HBV)感染是全球一项重大的公共卫生负担。尽管目前的治疗方法能够控制疾病进展,但由于治疗期间会产生耐药性且停药后常出现病毒再激活,因此需要终身治疗和监测。这样一来,肝细胞癌的发生率虽有所降低,但并未消除。HBV治疗失败的一个主要原因是无法根除或灭活病毒共价闭合环状DNA(cccDNA),它是病毒基因组的一种稳定的游离形式,由宿主组蛋白和非组蛋白修饰。越来越多的证据表明,cccDNA的表观遗传修饰有助于病毒复制及慢性HBV感染的转归。在此,我们通过借鉴癌症和其他病毒疾病的表观遗传疗法,总结HBV表观遗传学研究的当前进展及其对慢性HBV感染的治疗意义,这可能为治愈慢性乙型肝炎开辟新途径。(《肝脏病学》2017年;66卷:2066 - 2077页)