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

European Journal of Medicinal Chemistry
Rukang ZhangCheng Luo

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.

Citations

Jan 17, 2020·Liver International : Official Journal of the International Association for the Study of the Liver·Nicolas PotéValérie Paradis
Nov 27, 2020·Journal of Experimental & Clinical Cancer Research : CR·Shejuan AnAmanda M Saratsis
Dec 3, 2020·Frontiers in Oncology·Donglu WuDa Liu

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