聚adp核糖聚合酶抑制剂在卵巢癌中的临床应用

Dimple R. Bhatia, Sudeep Gupta
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引用次数: 0

摘要

聚(adp -核糖)聚合酶(PARP)抑制剂是近年来卵巢癌最有前途的靶向治疗方法。大约30%至50%的这些癌症的特征是由于肿瘤抑制基因BRCA1或BRCA2突变导致的异常DNA修复途径。PARP抑制剂治疗BRCA缺陷肿瘤的方法利用了一种针对同源重组DNA修复途径缺陷的合成致死策略。这篇简短的综述概述了BRCAness在维持基因组完整性方面的作用,PARP在DNA修复中的作用,PARP抑制剂作为单一疗法或与其他疗法联合使用的效用,对PARP抑制剂的耐药机制以及PARP抑制剂在卵巢癌治疗中的临床应用的生物标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Utility of Poly (ADP-Ribose) Polymerase Inhibitors in Ovarian Cancer
Inhibitors of the enzyme poly (ADP-ribose) polymerase (PARP) are the most promising class of targeted therapies in ovarian cancers in recent times. Approximately 30% to 50% of these cancers are characterized by aberrant DNA repair pathways due to mutations in tumor suppressor genes: BRCA1 or BRCA2. Therapeutic approach with PARP inhibitors in BRCA deficient tumors exploits a synthetic lethal strategy targeting the deficiency in homologous recombination DNA repair pathway. This short review provides an overview of BRCAness in maintaining genomic integrity, the role of PARP in DNA repair, utility of PARP inhibitors as monotherapy or in combination with other therapies, mechanisms of resistance to PARP inhibitors and biomarkers for clinical utility of PARP inhibitors in management of ovarian cancer.
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