Targeting epigenetics and lncRNAs in liver disease: From mechanisms to therapeutics

Pharmacol Res. 2021 Oct:172:105846. doi: 10.1016/j.phrs.2021.105846. Epub 2021 Aug 24.

Abstract

Early onset and progression of liver diseases can be driven by aberrant transcriptional regulation. Different transcriptional regulation processes, such as RNA/DNA methylation, histone modification, and ncRNA-mediated targeting, can regulate biological processes in healthy cells, as well also under various pathological conditions, especially liver disease. Numerous studies over the past decades have demonstrated that liver disease has a strong epigenetic component. Therefore, the epigenetic basis of liver disease has challenged our knowledge of epigenetics, and epigenetics field has undergone an important transformation: from a biological phenomenon to an emerging focus of disease research. Furthermore, inhibitors of different epigenetic regulators, such as m6A-related factors, are being explored as potential candidates for preventing and treating liver diseases. In the present review, we summarize and discuss the current knowledge of five distinct but interconnected and interdependent epigenetic processes in the context of hepatic diseases: RNA methylation, DNA methylation, histone methylation, miRNAs, and lncRNAs. Finally, we discuss the potential therapeutic implications and future challenges and ongoing research in the field. Our review also provides a perspective for identifying therapeutic targets and new hepatic biomarkers of liver disease, bringing precision research and disease therapy to the modern era of epigenetics.

Keywords: DNA methylation; Epigenetics; Histone modification; Liver disease; LncRNAs; RNA methylation.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adenosine / analogs & derivatives
  • Animals
  • Epigenesis, Genetic
  • Humans
  • Liver Diseases / genetics*
  • Liver Diseases / therapy
  • RNA, Long Noncoding*
  • Risk Factors

Substances

  • RNA, Long Noncoding
  • N-methyladenosine
  • Adenosine