4.6 Article

Bromodomain Drug Discovery - the Past, the Present, and the Future

期刊

CHEMICAL RECORD
卷 18, 期 12, 页码 1808-1817

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/tcr.201800074

关键词

drug discovery; bromodomains; epigenetics; BET-inhibitors; PROTACs; dual target inhibitors

资金

  1. DFG (Medical Epigenetics, and Research Training Group 1976) [GU1225/3-1, CRC992]

向作者/读者索取更多资源

With the bromodomain (BRD) inhibitor JQ1, a remarkable success story of BRD4 as a novel drug target has been set off that yielded many anti-cancer drugs that are now in clinical trials. But not all of the great prospects of BRDs as drug targets may become true. First evaluations of ongoing clinical trials revealed that treatment with BET-inhibitors can be accompanied with significant toxic side effects and the validation of the therapeutic benefit of BET-inhibitors compared to existing therapies is still pending. New strategies that may overcome possible obstacles in BRD drug discovery include combination therapies with other agents, dual target inhibitors, and proteolysis targeting chimeras (PROTACs). Furthermore, non-BET proteins seem promising drug targets as well. Most recently, BRDs have been identified as putative targets to treat parasitic diseases such as malaria. Milestones in BRD drug discovery are reviewed and promising new developments are evaluated.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据