Assays for pharmacodynamic analysis of histone deacetylase inhibitors

被引:13
作者
Chung, Eun Joo [1 ]
Lee, Min-Jung [1 ]
Lee, Sunmin [1 ]
Trepel, Jane B. [1 ]
机构
[1] NCI, Ctr Canc Res, NIH, Med Oncol Branch, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
acetylation; anticancer drugs; epigenetic therapy; histone deacetylase inhibitors; pharmacodynamic assays; transcription;
D O I
10.1517/17425255.2.2.213
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
Histone deacetylase inhibitors (HDACls) are a promising new class of targeted anticancer drugs. The pharmacodynamic (PD) assessment of whether a drug has hit its target is critically important to the successful development of any molecular targeted therapy. In the case of HDACls there are many issues to be considered in PD development and implementation. Although originally it was thought that measurement of core histone hyperacetylation in peripheral blood mononuclear cells might suffice as a PD marker, as the field is evolving it is becoming evident that other measures may be essential, and are likely to be tumour context specific. This paper provides an overview of the assays that have been performed thus far in HDACl clinical trials, with an analysis of relative strengths and weaknesses, and a delineation of the complexity of HDACl PD analysis. Consideration is given to where new approaches are needed and potential approaches for future monotherapy and combination therapy trials are suggested.
引用
收藏
页码:213 / 230
页数:18
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