Inhibition of histone deacetylases in cancer therapy: lessons from leukaemia

被引:207
作者
Ceccacci, Elena [1 ,2 ,3 ]
Minucci, Saverio [1 ,2 ,3 ]
机构
[1] European Inst Oncol, Dept Expt Oncol, Via Adamello 16, I-20139 Milan, Italy
[2] European Inst Oncol, Drug Dev Program, Via Adamello 16, I-20139 Milan, Italy
[3] Univ Milan, Dept Biosci, Via Celoria 26, I-20133 Milan, Italy
关键词
leukaemia; histone deacetylases; HDACi; cancer stem cells; APL; epigenetics; TRANS-RETINOIC ACID; ACETYLATION; HDAC1; DIFFERENTIATION; DISEASES; ROLES;
D O I
10.1038/bjc.2016.36
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Histone deacetylases (HDACs) are a key component of the epigenetic machinery regulating gene expression, and behave as oncogenes in several cancer types, spurring the development of HDAC inhibitors (HDACi) as anticancer drugs. This review discusses new results regarding the role of HDACs in cancer and the effect of HDACi on tumour cells, focusing on haematological malignancies, particularly acute myeloid leukaemia. Histone deacetylases may have opposite roles at different stages of tumour progression and in different tumour cell sub-populations (cancer stem cells), highlighting the importance of investigating these aspects for further improving the clinical use of HDACi in treating cancer.
引用
收藏
页码:605 / 611
页数:7
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