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本文引用的文献

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The microRNA-99 family modulates hepatitis B virus replication by promoting IGF-1R/PI3K/Akt/mTOR/ULK1 signaling-induced autophagy.微小RNA-99家族通过促进IGF-1R/PI3K/Akt/mTOR/ULK1信号诱导的自噬来调节乙型肝炎病毒复制。
Cell Microbiol. 2017 May;19(5). doi: 10.1111/cmi.12709. Epub 2017 Jan 5.
2
MicroRNA-939 restricts Hepatitis B virus by targeting Jmjd3-mediated and C/EBPα-coordinated chromatin remodeling.微小RNA-939通过靶向Jmjd3介导的和C/EBPα协调的染色质重塑来限制乙型肝炎病毒。
Sci Rep. 2016 Oct 25;6:35974. doi: 10.1038/srep35974.
3
MicroRNA miR-204 and miR-1236 inhibit hepatitis B virus replication via two different mechanisms.微小 RNA miR-204 和 miR-1236 通过两种不同的机制抑制乙型肝炎病毒的复制。
Sci Rep. 2016 Oct 13;6:34740. doi: 10.1038/srep34740.
4
Hepatitis B virus X induces inflammation and cancer in mice liver through dysregulation of cytoskeletal remodeling and lipid metabolism.乙型肝炎病毒X通过细胞骨架重塑和脂质代谢失调在小鼠肝脏中诱发炎症和癌症。
Oncotarget. 2016 Oct 25;7(43):70559-70574. doi: 10.18632/oncotarget.12372.
5
Impact of hepatitis B virus infection on hepatic metabolic signaling pathway.乙型肝炎病毒感染对肝脏代谢信号通路的影响。
World J Gastroenterol. 2016 Sep 28;22(36):8161-7. doi: 10.3748/wjg.v22.i36.8161.
6
miR-370 suppresses HBV gene expression and replication by targeting nuclear factor IA.miR-370 通过靶向核因子 IA 抑制 HBV 基因表达和复制。
J Med Virol. 2017 May;89(5):834-844. doi: 10.1002/jmv.24695. Epub 2016 Oct 3.
7
Epigenetically regulated miR-449a enhances hepatitis B virus replication by targeting cAMP-responsive element binding protein 5 and modulating hepatocytes phenotype.表观遗传调控的 miR-449a 通过靶向 cAMP 反应元件结合蛋白 5 并调节肝细胞表型来增强乙型肝炎病毒复制。
Sci Rep. 2016 May 3;6:25389. doi: 10.1038/srep25389.
8
Serum microRNA-125b correlates with hepatitis B viral replication and liver necroinflammation.血清 microRNA-125b 与乙型肝炎病毒复制和肝坏死性炎症相关。
Clin Microbiol Infect. 2016 Apr;22(4):384.e1-384.e10. doi: 10.1016/j.cmi.2015.12.024. Epub 2016 Jan 21.
9
MicroRNA-34c targets TGFB-induced factor homeobox 2, represses cell proliferation and induces apoptosis in hepatitis B virus-related hepatocellular carcinoma.微小RNA-34c靶向转化生长因子β诱导因子同源盒2,抑制乙型肝炎病毒相关肝细胞癌的细胞增殖并诱导其凋亡。
Oncol Lett. 2015 Nov;10(5):3095-3102. doi: 10.3892/ol.2015.3649. Epub 2015 Aug 27.
10
Hepatitis B Virus X Protein Induces Hepatic Steatosis by Enhancing the Expression of Liver Fatty Acid Binding Protein.乙型肝炎病毒X蛋白通过增强肝脏脂肪酸结合蛋白的表达诱导肝脂肪变性。
J Virol. 2015 Dec 4;90(4):1729-40. doi: 10.1128/JVI.02604-15. Print 2016 Feb 15.

微小RNA在肝细胞代谢及乙型肝炎病毒复制中的作用

The role of microRNAs in hepatocyte metabolism and hepatitis B virus replication.

作者信息

Deng Wanyu, Lu Mengji

机构信息

College of Life Science, Shangrao Normal University, Shangrao, 334001, China.

Institute of Virology, University Hospital of Essen, University of Duisburg-Essen, Essen, 45147, Germany.

出版信息

Virol Sin. 2016 Dec;31(6):472-479. doi: 10.1007/s12250-016-3924-0. Epub 2016 Dec 28.

DOI:10.1007/s12250-016-3924-0
PMID:28063013
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8193420/
Abstract

Though efficient vaccines against hepatitis B virus (HBV) and antiviral therapies are available, chronic HBV infection is still a global health problem. The process of HBV infection and HBV life cycle are extensively studied in last decades, however, the mechanisms of HBV-induced alterations of host cell metabolisms and host factors involved in modulating of viral replication are not fully understood. Thus, it is an important issue to examine these specific HBV-host interactions for development of novel strategies for antiviral therapies. Recently, microRNAs (miRNAs), a class of post-transcriptional regulatory small RNA, seem to be the relevant fine tuning factors of various cellular activities and pathways, including cell growth, metabolism, and viral replication. In this review, we summarize the up to date knowledge concerning the virus-host interactions and emphasizing on the role of miRNAs in regulation of HBV replication and host cell metabolism.

摘要

尽管有针对乙型肝炎病毒(HBV)的高效疫苗和抗病毒疗法,但慢性HBV感染仍然是一个全球性的健康问题。在过去几十年中,人们对HBV感染过程和HBV生命周期进行了广泛研究,然而,HBV诱导宿主细胞代谢改变的机制以及参与调节病毒复制的宿主因子尚未完全了解。因此,研究这些特定的HBV-宿主相互作用对于开发新的抗病毒治疗策略是一个重要问题。最近,微小RNA(miRNA),一类转录后调控的小RNA,似乎是各种细胞活动和途径(包括细胞生长、代谢和病毒复制)的相关微调因子。在这篇综述中,我们总结了关于病毒-宿主相互作用的最新知识,并着重阐述了miRNA在调节HBV复制和宿主细胞代谢中的作用。