Cancer treatment of the future: Inhibitors of histone methyltransferases

被引:71
作者
Spannhoff, Astrid [1 ]
Sippl, Wolfgang [2 ]
Jung, Manfred [1 ]
机构
[1] Univ Freiburg, Inst Pharmaceut Sci, D-79104 Freiburg, Germany
[2] Univ Halle Wittenberg, Inst Pharm, D-06120 Halle, Germany
关键词
Histone; Arginine methyltransferase; Lysine methyltransferase; Cancer treatment; Epigenetics; PRMT; PROTEIN ARGININE-METHYLTRANSFERASE; ANDROGEN-RECEPTOR; LYSINE METHYLATION; DEACETYLASE INHIBITORS; EXPRESSION; PROSTATE; DNA; PROLIFERATION; DEMETHYLATION; GENE;
D O I
10.1016/j.biocel.2008.07.024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer in humans is the result of a multi-step process. This process often involves the activation of oncogenes and/or the inactivation Of tumor suppressor genes. These two steps arise not only due to mutations, but Call also be the result of a translocation or an altered transcription rate. One important mechanism is the occurrence of epigenetic alterations like promotor methylation (which may lead to tumor suppressor silencing) or decreased histone acetylation (which may lead to tumor suppressor silencing) or proteins involved in apoptosis). Today, histone acetylation and DNA methylation are epigenetic modifications which have been linked closely to the pathology of human cancers and inhibitors of both enzyme classes for clinical use are at hand. In contrast,other fields of epigenetics still lack of similarly thorough knowledge. This is especially true for the group of histone methyltransferases and their inhibitors. Since connections between historic methylation patterns and cancer progression have been recognized. histone methyltransferases represent promising targets for future cancer treatment. (C) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4 / 11
页数:8
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