Sahai Vaibhav, Redig Amanda J, Collier Katharine A, Eckerdt Frank D, Munshi Hidayatullah G
Department of Medicine, University of Michigan Medical Center, Ann Arbor, MI, USA.
Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA, USA.
Oncotarget. 2016 Aug 16;7(33):53997-54009. doi: 10.18632/oncotarget.9804.
There is increasing interest in inhibitors targeting BET (bromodomain and extra-terminal) proteins because of the association between this family of proteins and cancer progression. BET inhibitors were initially shown to have efficacy in hematologic malignancies; however, a number of studies have now shown that BET inhibitors can also block progression of non-hematologic malignancies. In this Review, we summarize the efficacy of BET inhibitors in select solid tumors; evaluate the role of BET proteins in mediating resistance to current targeted therapies; and consider potential toxicities of BET inhibitors. We also evaluate recently characterized mechanisms of resistance to BET inhibitors; summarize ongoing clinical trials with these inhibitors; and discuss potential future roles of BET inhibitors in patients with solid tumors.
由于溴结构域和额外末端(BET)蛋白家族与癌症进展之间的关联,针对BET蛋白的抑制剂越来越受到关注。BET抑制剂最初显示出对血液系统恶性肿瘤有效;然而,现在许多研究表明,BET抑制剂也可以阻断非血液系统恶性肿瘤的进展。在本综述中,我们总结了BET抑制剂在特定实体瘤中的疗效;评估BET蛋白在介导对当前靶向治疗耐药性中的作用;并考虑BET抑制剂的潜在毒性。我们还评估了最近发现的对BET抑制剂耐药的机制;总结了这些抑制剂正在进行的临床试验;并讨论了BET抑制剂在实体瘤患者中的潜在未来作用。