The Emerging Therapeutic Potential of Histone Methyltransferase and Demethylase Inhibitors

被引:136
作者
Spannhoff, Astrid [1 ,2 ]
Hauser, Alexander-Thomas [1 ]
Heinke, Ralf [3 ]
Sippl, Wolfgang [3 ]
Jung, Manfred [1 ]
机构
[1] Univ Freiburg, Inst Pharmaceut Sci, D-79104 Freiburg, Germany
[2] Univ Texas MD Anderson Canc Ctr, Virginia Harris Cockrell Canc Res Ctr, Smithville, TX 78957 USA
[3] Univ Halle Wittenberg, Inst Pharm, D-06120 Halle, Saale, Germany
关键词
enzymes; epigenetics; histone demethylases; histone methyltransferases; medicinal-chemistry; ADENOSYLMETHIONINE-DEPENDENT METHYLTRANSFERASES; PROTEIN ARGININE METHYLTRANSFERASES; LYSINE-SPECIFIC DEMETHYLASE-1; MECHANISM-BASED INACTIVATOR; DOMAIN-CONTAINING PROTEINS; LINKED MENTAL-RETARDATION; ANDROGEN-RECEPTOR; STRUCTURAL BASIS; S-ADENOSYLMETHIONINE; MONOAMINE-OXIDASE;
D O I
10.1002/cmdc.200900301
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
Epigenetics is defined as heritable changes to the trascriptome that are independent of changes in the genome. The biochemical modification that govern epigenetics are DNA methylation and posttranslational histone modifications. Among the histone modifications, acetylation and deacetylation are well characterized whereas the fields of histone methylation and especially demethylation are still in their infancy. This is particularly true with regard to drug discovery. There is strong evidence that these modifications play an important role in the maintenance of transcription as well as in the development of certain diseases. This article gives an overview of the mechanisms of action of histone methyltransferases and demethylases, their role in the formation of certain diseases, and available inhibitors. Special emphasis is placed on the strategies that led to the first inhibitors which are currently availabale and the screening approaches that were used in that process.
引用
收藏
页码:1568 / 1582
页数:15
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