Antitumor activity of the dual BET and CBP/EP300 inhibitor NEO2734.
Ontology highlight
ABSTRACT: Bromodomain and extra-terminal domain (BET) proteins, cyclic adenosine monophosphate response element-binding protein (CBP), and the E1A-binding protein of p300 (EP300) are important players in histone acetylation. Preclinical evidence supports the notion that small molecules targeting these proteins individually or in combination can elicit antitumor activity. Here, we characterize the antitumor activity of the pan BET/CBP/EP300 inhibitor NEO2734 and provide insights into its mechanism of action through bromodomain-binding assays, in vitro and in vivo treatments of cancer cell lines, immunoblotting, and transcriptome analyses. In a panel of 60 models derived from different tumor types, NEO2734 exhibited antiproliferative activity in multiple cell lines, with the most potent activity obser
SUBMITTER: Spriano F
PROVIDER: S-EPMC7479962 | biostudies-literature | 2020 Sep
REPOSITORIES: biostudies-literature
ACCESS DATA