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N6-甲基腺苷RNA甲基化对病毒性肝炎的调控

Regulation of viral hepatitis by N6-methyladenosine RNA methylation.

作者信息

Moon Jae-Su, Siddiqui Aleem, Kim Geon-Woo

机构信息

Center for Rare Disease Therapeutic Technology, Therapeutics & Biotechnology Division, Korea Research Institute of Chemical Technology (KRICT), Daejeon, Korea.

Division of Infectious Diseases and Global Public Health, Department of Medicine, University of California San Diego, La Jolla, USA.

出版信息

Emerg Microbes Infect. 2025 Dec;14(1):2544726. doi: 10.1080/22221751.2025.2544726. Epub 2025 Aug 17.

Abstract

Recent studies have shown that the presence of an RNA modification, N6-methyladenosine (mA), in viral RNAs during infection significantly impacts the outcome of viral replication and pathogenesis. In particular, various functions of mA have been elucidated in hepatitis B virus (HBV), hepatitis C virus (HCV), and hepatitis delta virus (HDV). During viral infection, mA methylation not only directly affects the replication of these viruses but also regulates diverse cellular RNAs to control pathogenesis. This review aims to explore the functions of mA modification in the infectious processes and pathogenesis of HBV, HCV, and HDV. Understanding the role of mA methylation in these viral life cycles is essential for elucidating their pathogenesis and developing novel therapeutic strategies for HBV, HCV, and HDV infections.

摘要

最近的研究表明,感染期间病毒RNA中存在一种RNA修饰,即N6-甲基腺嘌呤(mA),会显著影响病毒复制和发病机制的结果。特别是,mA在乙型肝炎病毒(HBV)、丙型肝炎病毒(HCV)和丁型肝炎病毒(HDV)中的各种功能已得到阐明。在病毒感染期间,mA甲基化不仅直接影响这些病毒的复制,还调节多种细胞RNA以控制发病机制。本综述旨在探讨mA修饰在HBV、HCV和HDV感染过程及发病机制中的作用。了解mA甲基化在这些病毒生命周期中的作用对于阐明其发病机制以及开发针对HBV、HCV和HDV感染的新型治疗策略至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2d2b/12360054/4d9f01bfee75/TEMI_A_2544726_F0001_OC.jpg

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