临床肿瘤学杂志

• 综述与讲座 • 上一篇    下一篇

PARP抑制剂的临床研究进展

王均惠1,陈建新2,解方为1   

  1. 1 南京军区福州总医院肿瘤科 2 衢州市人民医院肿瘤内科
  • 收稿日期:2015-04-12 修回日期:2015-05-21 出版日期:2015-08-31 发布日期:2015-08-31
  • 通讯作者: 解方为

Clinical development of poly(ADP-ribose) polymerase inhibitors

WANG Junhui, CHEN Jianxin, XIE Fangwei.   

  1. Department of Oncology, Fuzhou General Hospital of Nanjing Military Command
  • Received:2015-04-12 Revised:2015-05-21 Online:2015-08-31 Published:2015-08-31
  • Contact: XIE Fangwei

摘要: 肿瘤细胞对化疗药物耐药是导致化疗失败的重要原因。肿瘤细胞DNA修复基因的过表达引起DNA损伤后修复并最终导致了耐药性的产生。聚腺苷酸二磷酸核糖基聚合酶(PARP)是具有碱基切除修复功能的DNA单链损伤修复酶,由于其在肿瘤细胞内过表达并在肿瘤细胞DNA损伤修复过程中发挥着重要作用,被认为是肿瘤靶向治疗领域的重要靶点。近年来关于PARP抑制剂的研究屡见报道,发现PARP抑制剂不仅对放化疗具有一定的增敏效果,且在特定基因型瘤种中还具有显著的单独抗肿瘤效应。本文旨在对近年来PARP抑制剂的最新临床研究进展进行综述。

Abstract: Chemo-resistance is one of the most importance reasons to explain the failure of chemotherapy. The over expression of DNA repairing gene in cancer cells lead to the chemoresistance. Poly(ADP-ribose) polymerase(PARP) is one of the DNA repairing enzymes by excising base which has been supposed to be one of the target of molecular targeting therapy. Recently plenty of PARP-related researches had been reported, which suggested that PARP inhibitors could sensitize chemotherapeutics as well as the antitumor effect alone. The text below will summarize the updating clinical researches of PARP inhibitors in recent 5 years.

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