HDAC modulation and cell death in the clinic

被引:74
作者
Dell'Aversana, Carmela [1 ]
Lepore, Ilaria [2 ]
Altucci, Lucia [1 ,2 ]
机构
[1] CNR IGB, I-80131 Naples, Italy
[2] Univ Naples 2, Dipartimento Patol Gen, I-80138 Naples, Italy
关键词
Histone deacetylases; Histone deacetylase inhibitors; Cancer; Clinical trials; HISTONE-DEACETYLASE INHIBITOR; SUBEROYLANILIDE HYDROXAMIC ACID; ACUTE MYELOID-LEUKEMIA; COLON-CANCER CELLS; PHASE-II TRIAL; REFRACTORY MULTIPLE-MYELOMA; CHRONIC LYMPHOCYTIC-LEUKEMIA; CLASSICAL HODGKINS LYMPHOMA; ACUTE MYELOGENOUS LEUKEMIA; TRAIL-INDUCED APOPTOSIS;
D O I
10.1016/j.yexcr.2012.01.025
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Histone acetyltransferases (HATs) and histone deacetylases (HDACs) are two opposing classes of enzymes, which finely regulate the balance of histone acetylation affecting chromatin packaging and gene expression. Imbalanced acetylation has been associated with carcinogenesis and cancer progression. In contrast to genetic mutations, epigenetic changes are potentially reversible. This implies that epigenetic alterations are amenable to pharmacological interventions. Accordingly, some epigenetic-based drugs (epidrugs) have been approved by the Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for cancer treatment. Here, we focus on the biological features of HDAC inhibitors (HDACis), analyzing the mechanism(s) of action and their current use in clinical practice. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:1229 / 1244
页数:16
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