| Literature DB >> 33174480 |
Zhongqi Cui1, Nan Huang1, Li Liu2, Xue Li1, Guohui Li3, Yan Chen1, Qi Wu1, Jie Zhang1, Shuping Long1, Minyi Wang1, Fenyong Sun1, Yi Shi2, Qiuhui Pan4.
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.Entities:
Keywords: N6-methyladenosine; differentially methylated genes; hepatic fibrosis progression; hepatic fibrosis reversal
Year: 2020 PMID: 33174480 DOI: 10.2217/epi-2019-0365
Source DB: PubMed Journal: Epigenomics ISSN: 1750-192X Impact factor: 4.778