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Roles of N6‐methyladenosine epitranscriptome in non‐alcoholic fatty liver disease and hepatocellular carcinoma

Authors :
Yuyan Chen
Zhengyi Zhu
Lu Zhang
Jinglin Wang
Haozhen Ren
Source :
Smart Medicine, Vol 2, Iss 3, Pp n/a-n/a (2023)
Publication Year :
2023
Publisher :
Wiley-VCH, 2023.

Abstract

Abstract Non‐alcoholic fatty liver disease (NAFLD) is a typical chronic liver disease connected to a high risk of developing hepatocellular carcinoma (HCC). The development of NAFLD and HCC has been associated with changes in epigenetics, such as histone modifications and micro RNA (miRNA)‐mediated processes. Recently, in the realm of epitranscriptomics, RNA alterations have become important regulators. N6‐methyladenosine (m6A) is the most common and crucial alteration for controlling mRNA stability, splicing, and translation. It is particularly important for controlling liver disease progression and hepatic function. This review aims to conclude recent research on the functions of m6A epitranscriptome in the molecular mechanisms behind NAFLD and HCC development, with special attention to the effects of m6A alteration on how HCC develops and its possible roles in the progression of NAFLD to HCC. Additionally, the review discusses the possible effects of m6A alteration on the treatment and diagnostic of NAFLD and HCC. It is crucial to remember that m6A modification is a reversible action controlled via the coordinated functions of the proteins that write and delete, enabling quick adaptability to environmental changes. The review also discusses m6A‐binding proteins' function in mRNA alternative splicing, translation, and degradation and their ability to modulate mRNA stability and processing. Understanding RNA modification regulation and its part in the emergence of HCC and NAFLD may provide new avenues for diagnosing and treating these diseases.

Details

Language :
English
ISSN :
27511871
Volume :
2
Issue :
3
Database :
Directory of Open Access Journals
Journal :
Smart Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.5dc7e4e1381e449b81abfd66a4b13091
Document Type :
article
Full Text :
https://doi.org/10.1002/SMMD.20230008