Shu Shaokun, Polyak Kornelia
Department of Medical Oncology, Dana-Farber Cancer Institute; Department of Medicine, Brigham and Women's Hospital; and Department of Medicine, Harvard Medical School, Boston, Massachusetts 02215.
Cold Spring Harb Symp Quant Biol. 2016;81:123-129. doi: 10.1101/sqb.2016.81.030908. Epub 2017 Jan 6.
Epigenetic regulators are emerging therapeutic targets in a wide variety of human cancers. BET bromodomain proteins have been identified as key regulators of oncogenic transcription factors including MYC; therefore, their inhibition might provide a way to block these "undruggable" targets. Several BET bromodomain inhibitors are in clinical development with promising preliminary findings. However, tumors acquire resistance to these agents in several different ways. In this review, we summarize the role that BET bromodomain proteins play in tumorigenesis as well as the molecular mechanisms underlying therapeutic responses and resistance to their inhibition with emphasis on BRD4 and breast cancer.
表观遗传调节因子正在成为多种人类癌症中的治疗靶点。BET溴结构域蛋白已被确定为包括MYC在内的致癌转录因子的关键调节因子;因此,抑制它们可能提供一种阻断这些“难以成药”靶点的方法。几种BET溴结构域抑制剂正在进行临床开发,初步结果很有前景。然而,肿瘤会通过几种不同的方式对这些药物产生耐药性。在本综述中,我们总结了BET溴结构域蛋白在肿瘤发生中的作用,以及治疗反应和对其抑制产生耐药性的分子机制,重点是BRD4和乳腺癌。