Therapeutic potential of ALKB homologs for cardiovascular disease

Biomed Pharmacother. 2020 Nov:131:110645. doi: 10.1016/j.biopha.2020.110645. Epub 2020 Sep 14.

Abstract

Cardiovascular diseases (CVDs) are the leading causes of human death. Recently, ALKB homologs, including ALKBH1-8 and FTO, have been found to have a variety of biological functions, such as histone demethylation, RNA demethylation, and DNA demethylation. These functions may regulate the physiological and pathological processes of CVDs, including inflammation, oxidative stress, cell apoptosis, and mitochondrial, endothelial, and fat metabolism dysfunction. In the present review, we summarize the biological functions of ALKB homologs and the relationship between the ALKB homologs and CVDs. Importantly, we discuss the roles of ALKB homologs in the regulation of oxidative stress, inflammation, autophagy, and DNA damage in CVDs, as well as the practical applications of ALKB homologs inhibitors or agonists in treating CVDs. In conclusion, the ALKBH family might be a promising target for CVDs therapy.

Keywords: ALKB homologs; Cardiovascular diseases; DNA demethylation; Oxidative stress; RNA demethylation; Therapy.

Publication types

  • Review

MeSH terms

  • AlkB Enzymes / administration & dosage*
  • AlkB Enzymes / chemistry*
  • AlkB Enzymes / metabolism
  • Animals
  • Cardiovascular Diseases / drug therapy*
  • Cardiovascular Diseases / metabolism
  • DNA Damage / drug effects
  • DNA Damage / physiology
  • DNA Methylation / drug effects
  • DNA Methylation / physiology
  • DNA Repair / drug effects
  • DNA Repair / physiology
  • Drug Delivery Systems / trends*
  • Humans
  • Oxidative Stress / drug effects
  • Oxidative Stress / physiology
  • Protein Structure, Secondary

Substances

  • AlkB Enzymes