Inhibitors of enzymes catalyzing modifications to histone lysine residues: structure, function and activity

Future Med Chem. 2016 May;8(8):879-97. doi: 10.4155/fmc-2016-0021. Epub 2016 May 13.

Abstract

Gene expression is partly controlled by epigenetic mechanisms including histone-modifying enzymes. Some diseases are caused by changes in gene expression that can be mitigated by inhibiting histone-modifying enzymes. This review covers the enzyme inhibitors targeting histone lysine modifications. We summarize the enzymatic mechanisms of histone lysine acetylation, deacetylation, methylation and demethylation and discuss the biochemical roles of these modifications in gene expression and in disease. We discuss inhibitors of lysine acetylation, deacetylation, methylation and demethylation defining their structure-activity relationships and their potential mechanisms. We show that there are potentially indiscriminant off-target effects on gene expression even with the use of selective epigenetic enzyme inhibitors.

Keywords: DOT1L; G9a; HDAC inhibitor; LSD1; epigenetics; histone; lysine acetyltransferase inhibitor; lysine demethylase inhibitor; lysine methyltransferase inhibitor; structure–activity relationship.

Publication types

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

MeSH terms

  • Enzyme Inhibitors / chemistry
  • Enzyme Inhibitors / pharmacology*
  • Epigenesis, Genetic / drug effects*
  • Histone Demethylases / antagonists & inhibitors*
  • Histone Demethylases / genetics
  • Histone Demethylases / metabolism
  • Histones / chemistry
  • Histones / metabolism*
  • Humans
  • Lysine / metabolism*
  • Molecular Structure
  • Structure-Activity Relationship

Substances

  • Enzyme Inhibitors
  • Histones
  • Histone Demethylases
  • Lysine