A natural compound, aristoyagonine, is identified as a potent bromodomain inhibitor by mid-throughput screening

Abstract Bromodomain-containing protein 4 ( Brd4) is known to play a key role in tumorigenesis. It binds acetylated histones to regulate the expression of numerous genes. Because of the importance of brd4in tumorigenesis, much research has been undertaken to develop brd4inhibitors with therapeutic potential. As a result, various scaffolds for bromodomaininhibitors have been identified. To discover new scaffolds, we performed mid-throughput screening using two different enzyme assays, alpha-screen and ELISA. We found a novel bromodomaininhibitor with a unique scaffold, aristoyagonine. This natural compound showed inhibitory activity in vitro and tumor growth inhibition in a Ty82-xenograft mouse model. In addition, we tested Brd4inhibitors in gastric cancer cell lines, and found that aristoyagonine exerted cytotoxicity not only in I-BET-762-sensitive cancer cells, but also in I-BET-762- resistant cancercells. This is the first paper to describe a natural compound as a Brd4 bromodomaininhibitor.