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

  • Rukang Zhang
  • , Jiang Wang
  • , Liang Zhao
  • , Shien Liu
  • , Daohai Du
  • , Hong Ding
  • , Shijie Chen
  • , Liyan Yue
  • , Yu Chih Liu
  • , Chenhua Zhang
  • , Hong Liu*
  • , Cheng Luo
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

13 Scopus citations

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.

Original languageEnglish
Pages (from-to)867-876
Number of pages10
JournalEuropean Journal of Medicinal Chemistry
Volume157
DOIs
StatePublished - 5 Sep 2018
Externally publishedYes

Keywords

  • Epigenetics
  • High throughput screening
  • Histone acetyltransferase
  • Inhibitor
  • MOF

Fingerprint

Dive into the research topics of 'Identification of novel inhibitors of histone acetyltransferase hMOF through high throughput screening'. Together they form a unique fingerprint.

Cite this