Identification of novel inhibitors of histone acetyltransferase hMOF through high throughput screening

被引:12
作者
Zhang, Rukang [1 ,2 ]
Wang, Jiang [1 ]
Zhao, Liang [1 ]
Liu, Shien [3 ]
Du, Daohai [1 ]
Ding, Hong [1 ]
Chen, Shijie [1 ]
Yue, Liyan [1 ]
Liu, Yu-Chih [4 ]
Zhang, Chenhua [4 ]
Liu, Hong [1 ]
Luo, Cheng [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, State Key Lab Drug Res, CAS Key Lab Receptor Res, 555 Zuchongzhi Rd, Shanghai 201203, Peoples R China
[2] Univ Chinese Acad Sci, 19 Yuquan Rd, Beijing 100049, Peoples R China
[3] WuXi AppTec, 288 Fute Zhong Rd, Shanghai 200131, Peoples R China
[4] Shanghai ChemPartner Co Ltd, 5 Bldg,998 Halei Rd, Shanghai 201203, Peoples R China
基金
中国国家自然科学基金;
关键词
High throughput screening; Epigenetics; Histone acetyltransferase; MOF; Inhibitor; GLOBAL GENE-EXPRESSION; CHROMATIN TRANSCRIPTION; BIOLOGICAL EVALUATION; LUNG-CANCER; PROTEIN; ACETYLATION; REPRESSES; GCN5; MOF; DESIGN;
D O I
10.1016/j.ejmech.2018.08.026
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The histone acetyltransferases (HATS) in mammals include GCN5 N-acetyltransferases, the MOZ, YBF2, SAS2, and TIP60 proteins, and the orphan HATs. The males absent on the first (MOF) is mainly related to acetylation of histone H4 Lys16 and has influence on downstream genes expression. However, the only inhibitor MG149 presented low activity against MOF. Besides, there was no high throughput screening platform on MOF, which limited the inhibitor discovery and functional study. In our study, we set up a high throughput screening platform based on amplified luminescent proximity homogeneous assay (ALPHA), which led us to a moderate inhibitor DC_M01. By chemical modification, we found DC_M01_7, which was the analog of DC_M01 with an IC50 value of 6 mu M. DC_M01_7 significantly inhibited HCT116 cells proliferation and could also inhibit histone 4 lysine 16 acetylation in HCT116 cells. To sum up, our work will probably assist the further development of more potent MOF inhibitors and the functional study of hMOF. (C) 2018 Published by Elsevier Masson SAS.
引用
收藏
页码:867 / 876
页数:10
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