Centre for Cancer Therapeutics, Ottawa Hospital Research Institute, 501 Smyth Road, Ottawa, ON, Canada K1H 8L6.
J Oncol. 2010;2010:891059. doi: 10.1155/2010/891059. Epub 2010 Feb 22.
In sporadic epithelial ovarian cancer (EOC), the inactivation of BRCA1 through various mechanisms is a relatively common event. BRCA1 protein dysfunction results in the breakdown of various critical pathways in the cell, notably, the DNA damage response and repair pathway. Tumors from patients with BRCA1 germline mutations have an increased sensitivity to DNA damaging chemotherapeutic agents, such as cisplatin, due to defective DNA repair. Thus, inhibiting BRCA1 in sporadic EOC using novel targeted therapies is an attractive strategy for the treatment of advanced or recurrent EOC. Several classes of small molecule inhibitors that affect BRCA1 have now been tested in preclinical and clinical studies suggesting that this is a rational therapeutic approach. The aim of this paper is to provide an understanding of how BRCA1 has evolved into a promising target for the treatment of sporadic disease and to outline the main potential small molecule inhibitors of BRCA1 in EOC.
在散发性上皮性卵巢癌(EOC)中,BRCA1 通过各种机制失活是一个相对常见的事件。BRCA1 蛋白功能障碍导致细胞内各种关键途径的崩溃,特别是 DNA 损伤反应和修复途径。由于 DNA 修复缺陷,来自具有 BRCA1 种系突变的患者的肿瘤对 DNA 损伤化疗药物(如顺铂)具有更高的敏感性。因此,使用新型靶向治疗抑制散发性 EOC 中的 BRCA1 是治疗晚期或复发性 EOC 的一种有吸引力的策略。现已在临床前和临床研究中测试了几类影响 BRCA1 的小分子抑制剂,这表明这是一种合理的治疗方法。本文的目的是提供对 BRCA1 如何演变为治疗散发性疾病的有前途的靶标的理解,并概述 EOC 中 BRCA1 的主要潜在小分子抑制剂。