Focus on acetylation: the role of histone deacetylase inhibitors in cancer therapy and beyond

被引:35
作者
Konstantinopoulos, Panagiotis A. [1 ]
Karamouzis, Michalis V. [1 ]
Papavassiliou, Athanasios G. [1 ]
机构
[1] Univ Athens, Sch Med, Dept Biol Chem, GR-11527 Athens, Greece
关键词
acetylation; HAT; HDAC; HDAC inhibitors;
D O I
10.1517/13543784.16.5.569
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Reversal of tumorigenic epigenetic alterations is an exciting strategy for anticancer drug development. Pharmacologic inhibition of histone deacetylases (HDACs) induces differentiation, proliferation arrest and apoptosis of cancer cells. in addition to their effects on histones, HDAC inhibitors increase the acetylation level of several non-histone proteins, such as transcription factors, cytoskeletal proteins and molecular chaperones, which are crucial in tumorigenesis. Most importantly, the therapeutic potential of HDAC inhibitors goes well beyond carcinogenesis and may include neurodegenerative and inflammatory disorders. This editorial discusses the implication of HDACs in carcinogenesis, the molecular basis of the selectivity of HDAC inhibitors and their possible therapeutic role in non-malignant pathologic conditions.
引用
收藏
页码:569 / 571
页数:3
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