| Literature DB >> 32396836 |
Ali Bayoumi1, Henning Grønbæk2, Jacob George1, Mohammed Eslam3.
Abstract
Despite decades of research, effective therapies for metabolic (dysfunction)-associated fatty liver disease (MAFLD) are lacking. An increasing body of evidence suggests that epigenetic dysregulation is frequent in MAFLD, and orchestrates many aspects of its development and progression. Furthermore, the high plasticity of epigenetic modifications in response to environmental cues renders epigenetics a novel area for therapeutic drug discovery. Over recent years, several epigenetics-based drugs and diagnostic biomarkers have entered clinical development and/or obtained regulatory approval. Here, we review recent advances in our understanding of epigenetic regulation and programming during MAFLD, including DNA methylation, histone modifications, chromatin remodelling, transcriptional control, and noncoding (nc)RNAs. We also discuss the potential translational implications and challenges of epigenetics in the context of MAFLD.Entities:
Keywords: DNA methylation; MAFLD; NAFLD; epigenetics; fibrosis
Mesh:
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Year: 2020 PMID: 32396836 DOI: 10.1016/j.tig.2020.03.003
Source DB: PubMed Journal: Trends Genet ISSN: 0168-9525 Impact factor: 11.639