Epigenetic therapy: histone acetylation, DNA methylation and anti-cancer drug discovery
- PMID: 20025605
- DOI: 10.2174/156800909790192428
Epigenetic therapy: histone acetylation, DNA methylation and anti-cancer drug discovery
Abstract
Histone proteins are subject to a diverse range of post-translational modifications which, along with DNA methylation, play a major role in controlling gene expression, cell division, survival and differentiation. Alterations in these chromatin modifications are thought to contribute to important human diseases including cancer. Inhibition of the enzymes that introduce and remove these chromatin modifications is proving an effective approach to cancer therapy and inhibitors of histone deacetylases and DNA methyltransferases have been approved for use in haematological malignancies. Here we provide a background to the biology of chromatin modifications and review some of the evidence validating histone deacetylases and DNA methyltransferases as targets for anti-cancer drug discovery. We then focus on two of the key issues in this field; the identification of novel inhibitors to overcome shortcomings of first generation agents and the potential role of histone deacetylase and DNA methyltransferase inhibitors in combination therapies for oncology. Finally, we highlight some of the challenges that will need to addressed to further progress the development of epigenetic-based therapies for cancer.
Similar articles
-
Histone modification therapy of cancer.Adv Genet. 2010;70:341-86. doi: 10.1016/B978-0-12-380866-0.60013-7. Adv Genet. 2010. PMID: 20920755 Review.
-
New anti-cancer strategies: epigenetic therapies and biomarkers.Front Biosci. 2005 May 1;10:1897-931. doi: 10.2741/1668. Front Biosci. 2005. PMID: 15769674 Review.
-
Epigenetics in cancer: targeting chromatin modifications.Mol Cancer Ther. 2009 Jun;8(6):1409-20. doi: 10.1158/1535-7163.MCT-08-0860. Epub 2009 Jun 9. Mol Cancer Ther. 2009. PMID: 19509247 Review.
-
Epigenetic therapy of cancer with histone deacetylase inhibitors.J Cancer Res Ther. 2014 Jul-Sep;10(3):469-78. doi: 10.4103/0973-1482.137937. J Cancer Res Ther. 2014. PMID: 25313724 Review.
-
Inhibitors of DNA Methylation, Histone Deacetylation, and Histone Demethylation: A Perfect Combination for Cancer Therapy.Adv Cancer Res. 2016;130:55-111. doi: 10.1016/bs.acr.2016.01.007. Epub 2016 Mar 2. Adv Cancer Res. 2016. PMID: 27037751 Review.
Cited by
-
Inhibition of histone deacetylase activity in human endometrial stromal cells promotes extracellular matrix remodelling and limits embryo invasion.PLoS One. 2012;7(1):e30508. doi: 10.1371/journal.pone.0030508. Epub 2012 Jan 26. PLoS One. 2012. PMID: 22291969 Free PMC article.
-
Epigenetic regulation of mesenchymal stem cells: a focus on osteogenic and adipogenic differentiation.Stem Cells Int. 2011;2011:201371. doi: 10.4061/2011/201371. Epub 2011 Jul 11. Stem Cells Int. 2011. PMID: 21772852 Free PMC article.
-
PCI-24781 (abexinostat), a novel histone deacetylase inhibitor, induces reactive oxygen species-dependent apoptosis and is synergistic with bortezomib in neuroblastoma.J Cancer Ther Res. 2013 Dec 28;2:21. doi: 10.7243/2049-7962-2-21. J Cancer Ther Res. 2013. PMID: 25520806 Free PMC article.
-
Histone deacetylase inhibition redistributes topoisomerase IIβ from heterochromatin to euchromatin.Nucleus. 2011 Jan-Feb;2(1):61-71. doi: 10.4161/nucl.2.1.14194. Nucleus. 2011. PMID: 21647300 Free PMC article.
-
Polymer model integrates imaging and sequencing to reveal how nanoscale heterochromatin domains influence gene expression.Nat Commun. 2025 Apr 23;16(1):3816. doi: 10.1038/s41467-025-59001-z. Nat Commun. 2025. PMID: 40268925 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources