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Identification of catalytic and non‐catalytic activity inhibitors against PRC2‐EZH2 complex through multiple high‐throughput screening campaigns
Author(s) -
Zhou Yan,
Du DaoHai,
Wang Jia,
Cai XiaoQing,
Deng Alicia X.,
Nosjean Olivier,
Boutin Jean A.,
Renard Pierre,
Yang DeHua,
Luo Cheng,
Wang MingWei
Publication year - 2020
Publication title -
chemical biology and drug design
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.59
H-Index - 77
eISSN - 1747-0285
pISSN - 1747-0277
DOI - 10.1111/cbdd.13702
Subject(s) - prc2 , ezh2 , histone h3 , chemistry , histone , high throughput screening , psychological repression , mutant , acetylation , biology , biochemistry , gene , gene expression
Abstract Enhancer of zeste homolog 2 (EZH2) is the catalytic subunit of the polycomb repressive complex 2 (PRC2) along with embryonic ectoderm development (EED) and suppressor of zeste 12 (SUZ12), which implements transcriptional repression mainly by depositing trimethylation marks at lysine 27 of histone H3 (H3K27me3). Its catalytic activity is closely correlated with the stability of PRC2, and somatic activating mutation of EZH2 Y641F within the catalytic SET domain drives tumor aggressiveness, drug resistance, and poor prognosis. Here, we report two high‐throughput screening (HTS) campaigns targeting EZH2 Y641F and EZH2‐EED interaction, respectively. For the EZH2 Y641F mutant, the HTS campaign involved a library of 250,000 compounds using a homogenous time‐resolved fluorescence (HTRF) assay and identified 162 hits, while 60,160 compounds were screened against EZH2‐EED interaction with a fluorescence polarization (FP) assay resulting in 97 hits. Among the 162 EZH2 Y641F inhibitors, 38 also suppressed EZH2‐EED interaction and 80 showed inhibitory effects on the wide‐type (WT) EZH2. Meanwhile, 10 of the 97 EZH2‐EED interaction inhibitors were active against WT EZH2. These hit compounds provide useful tools for the development of novel PRC2‐EZH2 inhibitors targeting its catalytic and non‐catalytic activities.