Therapeutic potential of selective histone deacetylase 3 inhibition

Eur J Med Chem. 2019 Jan 15:162:534-542. doi: 10.1016/j.ejmech.2018.10.072. Epub 2018 Nov 17.

Abstract

Histone deacetylases (HDACs) are closely related to the occurrence and development of a variety of diseases, such as tumor, inflammation, diabetes mellitus, cardiovascular and neurodegenerative diseases. Inhibition of HDACs by developing HDAC inhibitors has achieved significant progress in the treatment of diseases caused by epigenetic abnormalities, and especially in the cancer therapy. Isoform selective HDAC inhibitors are emphasized to be disease specific and have less off-target effects and better safety performances. HDAC3 has been illustrated to play specific role in the development of several diseases, and the discovery of HDAC3 selective inhibitors has exhibited potential in the targeted disease treatment. Herein, we summarize the current knowledge about the prospects of selective inhibition of HDAC3 for the drug development.

Keywords: Cardiovascular disease; Diabetes; HDAC3 selective inhibitor; Inflammation; Neurodegenerative disease; Tumor.

Publication types

  • Review

MeSH terms

  • Cardiovascular Diseases / drug therapy
  • Diabetes Mellitus / drug therapy
  • Histone Deacetylase Inhibitors / pharmacology*
  • Histone Deacetylase Inhibitors / therapeutic use
  • Histone Deacetylases / chemistry
  • Histone Deacetylases / drug effects*
  • Humans
  • Inflammation / drug therapy
  • Neoplasms / drug therapy
  • Neurodegenerative Diseases / drug therapy
  • Protein Isoforms

Substances

  • Histone Deacetylase Inhibitors
  • Protein Isoforms
  • Histone Deacetylases
  • histone deacetylase 3