Institute of Pharmaceutical Sciences, Albert-Ludwigs-Universität Freiburg, Hermann-Herder-Str. 9, 79104, Freiburg, Germany.
Chem Rec. 2018 Dec;18(12):1808-1817. doi: 10.1002/tcr.201800074. Epub 2018 Oct 5.
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.
随着溴结构域(BRD)抑制剂 JQ1 的出现,BRD4 作为一个新的药物靶点取得了显著的成功,产生了许多正在临床试验中的抗癌药物。但并非 BRD 作为药物靶点的所有巨大前景都可能成为现实。对正在进行的临床试验的初步评估表明,BET 抑制剂的治疗可能伴随着明显的毒性副作用,并且 BET 抑制剂与现有疗法相比的治疗益处的验证仍在进行中。可能克服 BRD 药物发现中可能存在的障碍的新策略包括与其他药物联合治疗、双重靶标抑制剂和蛋白水解靶向嵌合体(PROTAC)。此外,非 BET 蛋白似乎也是有前途的药物靶点。最近,BRD 已被确定为治疗疟疾等寄生虫病的潜在靶点。本文回顾了 BRD 药物发现的里程碑,并评估了有前途的新进展。