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

作者：Kim Young Hun; Kim Minsung; Yoo Miyoun; Kim Ji Eun; Lee Heung Kyoung; Heo Jung Nyoung; Lee Chong Ock; Yoo Minjin; Jung Kwan Young; Yun Chang Soo; Moon Sung Woong; Chang Hye Kyung; Chung Chul Woong; Pyo Suhkneung; Choi Sang Un^*; Park Chi Hoon^*

来源：Biochemical and Biophysical Research Communications, 2018, 503(2): 882-887.

DOI：10.1016/j.bbrc.2018.06.091

• Aristoyagonine
• Bromodomain inhibitor
• Natural compound
• Cancer
• Mid-throughput screening

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 brd4 in tumorigenesis, much research has been undertaken to develop brd4 inhibitors with therapeutic potential. As a result, various scaffolds for bromodomain inhibitors 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 bromodomain inhibitor 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 Brd4 inhibitors 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 cancer cells. This is the first paper to describe a natural compound as a Brd4 bromodomain inhibitor.

• 出版日期2018-9-5