Inhibition of the HIF1α-p300 interaction by quinone- and indandione-mediated ejection of structural Zn(II)

被引:34
|
作者
Jayatunga, Madura K. P. [1 ]
Thompson, Sam [1 ]
McKee, Tawnya C. [2 ]
Chan, Mun Chiang [1 ]
Reece, Kelie M. [3 ]
Hardy, Adam P. [1 ]
Sekirnik, Rok [1 ]
Seden, Peter T. [1 ]
Cook, Kristina M. [3 ]
McMahon, James B. [2 ]
Figg, William D. [3 ]
Schofield, Christopher J. [1 ]
Hamilton, Andrew D. [1 ]
机构
[1] Univ Oxford, Chem Res Lab, Dept Chem, Oxford OX1 3TA, England
[2] Ctr Canc Res, Mol Targets Lab, Frederick Natl Lab Canc Res, Frederick, MD 21702 USA
[3] NCI, Mol Pharmacol Sect, Oncol Branch, Ctr Canc Res,NIH, Bethesda, MD 20892 USA
基金
美国国家卫生研究院; 英国惠康基金;
关键词
Hypoxia; HIF; p300/CBP; Zinc ejection; Electrophile; Quinone; HYPOXIA-INDUCIBLE TRANSCRIPTION; ENDOTHELIAL GROWTH-FACTOR; SMALL-MOLECULE INHIBITOR; DNA-BINDING; FACTOR-I; FACTOR; 1-ALPHA; TUMOR-GROWTH; PROTEIN; HIF-1; HYDROQUINONE;
D O I
10.1016/j.ejmech.2014.06.006
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Protein-protein interactions between the hypoxia inducible factor (HIF) and the transcriptional coactivators p300/CBP are potential cancer targets due to their role in the hypoxic response. A natural product based screen led to the identification of indandione and benzoquinone derivatives that reduce the tight interaction between a HIF-1 alpha fragment and the CH1 domain of p300. The indandione derivatives were shown to fragment to give ninhydrin, which was identified as the active species. Both the naphthoquinones and ninhydrin were observed to induce Zn(II) ejection from p300 and the catalytic domain of the histone demethylase KDM4A. Together with previous reports on the effects of related compounds on HIF-1 alpha and other systems, the results suggest that care should be taken in interpreting biological results obtained with highly electrophilic/thiol modifying compounds. (C) 2014 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:509 / 516
页数:8
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