Make your best BET: The emerging role of BET inhibitor treatment in malignant tumors

被引:84
作者
Bechter, Oliver [1 ,2 ]
Schoffski, Patrick [1 ,2 ]
机构
[1] Univ Hosp Leuven, Leuven Canc Inst, Dept Gen Med Oncol, Leuven, Belgium
[2] KU, Dept Oncol, Leuven, Belgium
关键词
Bromodomain; BET inhibition; NUT carcinoma; MYC; BET inhibitor combination; CHROMATIN-REMODELING COMPLEX; BROMODOMAIN PROTEIN BRD4; DNA-DAMAGE; SELECTIVE-INHIBITION; NUCLEAR PROTEINS; DOSE-ESCALATION; GENE-EXPRESSION; ACUTE-LEUKEMIA; BREAST-CANCER; UP-REGULATION;
D O I
10.1016/j.pharmthera.2020.107479
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Bromodomains are protein-protein interaction modules with a great diversity in terms of number of proteins and their function. The bromodomain and extraterminal protein (BET) represents a distinct subclass of bromodomain proteins mainly involved in transcriptional regulation via their interaction with acetylated chromatin. In cancer cells BET proteins are found to be altered in many ways such as overexpression, mutations and fusions of BET proteins or their interference with cancer relevant signaling pathways and transcriptional programs in order to sustain cancer growth and viability. Blocking BET protein function with small molecules is associated with therapeutic activity. Consequently, a variety of small molecules have been developed and a number of phase I clinical trials have explored their tolerability and efficacy in patients with solid tumors and hematological malignancies. We will review the rational for applying BET inhibitors in the clinic and we will discuss the toxicity profile as well as efficacy of this new class of protein inhibitors. We will also highlight the emerging problem of treatment resistance and the potential these drugs might have when combined with other anti-cancer therapies. (C) 2020 Elsevier Inc. All rights reserved.
引用
收藏
页数:14
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