cccDNA
表观遗传学
乙型肝炎病毒
肝细胞癌
病毒学
乙型肝炎
组蛋白
病毒
表观遗传疗法
环状DNA
病毒复制
免疫学
医学
生物
DNA甲基化
癌症研究
DNA
基因组
乙型肝炎表面抗原
遗传学
基因
基因表达
作者
Xupeng Hong,Elena S. Kim,Haitao Guo
出处
期刊:Hepatology
[Wiley]
日期:2017-11-06
卷期号:66 (6): 2066-2077
被引量:148
摘要
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. (H epatology 2017;66:2066–2077)
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