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Inhibitors of enzymes catalyzing modifications to histone lysine residues: structure, function and activity
- Source :
- Future Medicinal Chemistry. 8:879-897
- Publication Year :
- 2016
- Publisher :
- Future Science Ltd, 2016.
-
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.
- Subjects :
- 0301 basic medicine
Epigenetics in learning and memory
Epigenesis, Genetic
Histones
Structure-Activity Relationship
03 medical and health sciences
Drug Discovery
Humans
Epigenetics
Enzyme Inhibitors
Epigenomics
Histone Demethylases
Pharmacology
Molecular Structure
biology
Chemistry
Lysine
EZH2
DOT1L
030104 developmental biology
Histone
Biochemistry
Acetylation
Histone methyltransferase
biology.protein
Molecular Medicine
Subjects
Details
- ISSN :
- 17568927 and 17568919
- Volume :
- 8
- Database :
- OpenAIRE
- Journal :
- Future Medicinal Chemistry
- Accession number :
- edsair.doi.dedup.....c4aa3e463f53836dbe65b545c1a5d847
- Full Text :
- https://doi.org/10.4155/fmc-2016-0021