| Literature DB >> 30145373 |
Rukang Zhang1, Jiang Wang2, Liang Zhao2, Shien Liu3, Daohai Du2, Hong Ding2, Shijie Chen2, Liyan Yue2, Yu-Chih Liu4, Chenhua Zhang4, Hong Liu5, Cheng Luo6.
Abstract
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 μM. 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.Entities:
Keywords: Epigenetics; High throughput screening; Histone acetyltransferase; Inhibitor; MOF
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Year: 2018 PMID: 30145373 DOI: 10.1016/j.ejmech.2018.08.026
Source DB: PubMed Journal: Eur J Med Chem ISSN: 0223-5234 Impact factor: 6.514