Rational Combinations Using HDAC Inhibitors

被引:203
作者
Bots, Michael [1 ]
Johnstone, Ricky W. [1 ,2 ]
机构
[1] Peter MacCallum Canc Ctr, CancerTherapeut Program, Melbourne, Vic 3002, Australia
[2] Univ Melbourne, Melbourne, Vic 3010, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
HISTONE-DEACETYLASE INHIBITORS; ACUTE MYELOID-LEUKEMIA; BREAST-CANCER CELLS; VALPROIC ACID; CLINICAL-IMPLICATIONS; PROTEASOME INHIBITOR; DNA METHYLATION; RETINOIC ACID; BCR-ABL; THERAPEUTIC ACTIVITIES;
D O I
10.1158/1078-0432.CCR-08-2786
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
In addition to well-characterized genetic abnormalities that lead to cancer onset and progression, it is now recognized that alterations to the epigenome may also play a significant role in oncogenesis. As a result, epigenetic-modulating agents such as histone deacetylase inhibitors (HDACi) have attracted enormous attention as anticancer drugs. In numerous in vitro and preclinical settings, these compounds have shown their vast potential as single agent anticancer therapies, but unfortunately equivalent responses have not always been observed in patients. Given the pleiotropic effects HDACi have on malignant cells, their true therapeutic potential most likely lies in combination with other anticancer drugs. In this review we will focus on the anticancer effects of HDACi when combined with other cancer therapeutics with an emphasis on those combinations based on a strong molecular rationale.
引用
收藏
页码:3970 / 3977
页数:8
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