Emerging Epigenetic Targets and Therapies in Cancer Medicine
- 1 May 2012
- journal article
- review article
- Published by American Association for Cancer Research (AACR) in Cancer Discovery
- Vol. 2 (5) , 405-413
- https://doi.org/10.1158/2159-8290.cd-12-0076
Abstract
Abnormalities in the epigenetic regulation of chromatin structure and function can lead to aberrant gene expression and cancer development. Consequently, epigenetic therapies aim to restore normal chromatin modification patterns through the inhibition of various components of the epigenetic machinery. Histone deacetylase and DNA methyltransferase inhibitors represent the first putative epigenetic therapies; however, these agents have pleiotropic effects and it remains unclear how they lead to therapeutic responses. More recently, drugs that inhibit histone methyltransferases were developed, perhaps representing more specific agents. We review emerging epigenetic targets in cancer and present recent models of promising epigenetic therapies. Significance: The use of DNA methyltransferase and histone deacetylase inhibitors in patients has validated the use of drugs targeted to epigenetic enzymes and strengthened the need for development of additional therapies. In this review, we summarize recently discovered epigenetic abnormalities, their implications for cancer, and the approaches taken for discovering small-molecule inhibitors targeting various properties of the epigenetic machinery. Cancer Discov; 2(5); 405–13. ©2012 AACR.Keywords
This publication has 75 references indexed in Scilit:
- Menin-MLL inhibitors reverse oncogenic activity of MLL fusion proteins in leukemiaNature Chemical Biology, 2012
- NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression patternBlood, 2011
- H3K36 Methylation Antagonizes PRC2-mediated H3K27 MethylationJournal of Biological Chemistry, 2011
- Oncometabolite 2-Hydroxyglutarate Is a Competitive Inhibitor of α-Ketoglutarate-Dependent DioxygenasesCancer Cell, 2011
- Structural basis for G9a-like protein lysine methyltransferase inhibition by BIX-01294Nature Structural & Molecular Biology, 2009
- BRD–NUT oncoproteins: a family of closely related nuclear proteins that block epithelial differentiation and maintain the growth of carcinoma cellsOncogene, 2007
- NUP98–NSD1 links H3K36 methylation to Hox-A gene activation and leukaemogenesisNature Cell Biology, 2007
- The BCL6 proto-oncogene suppresses p53 expression in germinal-centre B cellsNature, 2004
- NUP98 is fused to the NSD3 gene in acute myeloid leukemia associated with t(8;11)(p11.2;p15)Blood, 2002
- NSD3, a New SET Domain-Containing Gene, Maps to 8p12 and Is Amplified in Human Breast Cancer Cell LinesGenomics, 2001