卵巢癌
合成致死
癌症
医学
生物信息学
聚ADP核糖聚合酶
奥拉帕尼
DNA损伤修复
DNA修复
癌症研究
生物
内科学
遗传学
DNA
聚合酶
出处
期刊:Journal of Cancer Science & Therapy
[OMICS Publishing Group]
日期:2013-01-01
卷期号:05 (11)
被引量:24
标识
DOI:10.4172/1948-5956.1000234
摘要
Ovarian cancer continues to be the main cause of death among all gynecological tumors.After standard treatments, most of patients are destined to recur within a short period, thus new therapies are urgently needed.The increasing knowledge of molecular mechanisms in ovarian cancer pathogenesis allowed identifying several targeted agents that are now entering in clinical practice.The family of poly(ADP-ribose) polymerase inhibitors represents a widely investigated and promising alternative for the targeted therapy of ovarian malignancies.PARP inhibitors exploit the synthetic lethality concept to prevent the repair of DNA damage, causing cancer cell death.This review describes the molecular mechanisms at the basis of PARP inhibition, particularly in BRCA-related ovarian malignancies and analyzes the main agents under investigations in preclinical and clinical studies.
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