Dynamic analysis of m6A methylation spectroscopy during progression and reversal of hepatic fibrosis

Author:

Cui Zhongqi1ORCID,Huang Nan1,Liu Li2,Li Xue1,Li Guohui3,Chen Yan1,Wu Qi1,Zhang Jie1,Long Shuping1,Wang Minyi1,Sun Fenyong1,Shi Yi2,Pan Qiuhui4

Affiliation:

1. Department of Clinical Laboratory, Shanghai Tenth People's Hospital, Tongji University, Shanghai 200072, China

2. Department of Clinical Laboratory, Shanghai Fourth People's Hospital affiliated to Tongji University School of Medicine, Shanghai 200081, China

3. Institute of Life Sciences, Jiangsu University, 301# Xuefu Road, Zhenjiang 212013, China

4. Department of Laboratory Medicine, Shanghai Children's Medical Center, Shanghai Jiaotong University School of Medicine, Shanghai 200127, China

Abstract

Aim: To dynamically analyze the differential m6A methylation during the progression and reversal of hepatic fibrosis. Materials & methods: We induced hepatic fibrosis in C57/BL6 mice by intraperitoneal injection of CCl4. The reversal model of hepatic fibrosis was established by stopping drug after continuous injection of CCl4. Dynamic m6A methylation was evaluated using MeRIP-Seq in the progression and reversal of hepatic fibrosis at different stages. Result: During the hepatic fibrosis, differential m6A methylation was mainly enriched in processes associated with oxidative stress and cytochrome metabolism, while differential m6A methylation was mainly enriched in processes associated with immune response and apoptosis in the hepatic fibrosis reversal. Conclusion: m6A methylation plays an important role in the progression and reversal of hepatic fibrosis.

Funder

National Natural Science Foundation of China

Shanghai Municipal Health Bureau

shanghai municipal health planning commission research fund

Publisher

Future Medicine Ltd

Subject

Cancer Research,Genetics

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