6YQN

Crystal structure of the first bromodomain of human BRD4 in complex with the dual inhibitor TW9

6YQN の概要

• エントリーDOI: 10.2210/pdb6yqn/pdb
• 分子名称: Bromodomain-containing protein 4, 1,2-ETHANEDIOL, ~{N}-(2-aminophenyl)-4-[2-[(9~{S})-7-(4-chlorophenyl)-4,5,13-trimethyl-3-thia-1,8,11,12-tetrazatricyclo[8.3.0.0^{2,6}]t rideca-2(6),4,7,10,12-pentaen-9-yl]ethanoylamino]benzamide, ... (4 entities in total)
• 機能のキーワード: bromodomain, brd4(bd1), dual bromodomain hdac inhibitor, structural genomics consortium, sgc, gene regulation
• 由来する生物種: Homo sapiens (Human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 15833.64

構造登録者

Joerger, A.C.,Balourdas, D.I.,Weiser, T.,Chatterjee, D.,Knapp, S.,Structural Genomics Consortium (SGC) (登録日: 2020-04-17, 公開日: 2020-05-06, 最終更新日: 2024-01-24)

主引用文献

Zhang, X.,Zegar, T.,Weiser, T.,Hamdan, F.H.,Berger, B.T.,Lucas, R.,Balourdas, D.I.,Ladigan, S.,Cheung, P.F.,Liffers, S.T.,Trajkovic-Arsic, M.,Scheffler, B.,Joerger, A.C.,Hahn, S.A.,Johnsen, S.A.,Knapp, S.,Siveke, J.T.
Characterization of a dual BET/HDAC inhibitor for treatment of pancreatic ductal adenocarcinoma.
Int.J.Cancer, 147:2847-2861, 2020

PubMed Abstract: Pancreatic ductal adenocarcinoma (PDAC) is resistant to virtually all chemo- and targeted therapeutic approaches. Epigenetic regulators represent a novel class of drug targets. Among them, BET and HDAC proteins are central regulators of chromatin structure and transcription, and preclinical evidence suggests effectiveness of combined BET and HDAC inhibition in PDAC. Here, we describe that TW9, a newly generated adduct of the BET inhibitor (+)-JQ1 and class I HDAC inhibitor CI994, is a potent dual inhibitor simultaneously targeting BET and HDAC proteins. TW9 has a similar affinity to BRD4 bromodomains as (+)-JQ1 and shares a conserved binding mode, but is significantly more active in inhibiting HDAC1 compared to the parental HDAC inhibitor CI994. TW9 was more potent in inhibiting tumor cell proliferation compared to (+)-JQ1, CI994 alone or combined treatment of both inhibitors. Sequential administration of gemcitabine and TW9 showed additional synergistic antitumor effects. Microarray analysis revealed that dysregulation of a FOSL1-directed transcriptional program contributed to the antitumor effects of TW9. Our results demonstrate the potential of a dual chromatin-targeting strategy in the treatment of PDAC and provide a rationale for further development of multitarget inhibitors.

PubMed: 32599645
DOI: 10.1002/ijc.33137

実験手法

X-RAY DIFFRACTION (1.05 Å)