国际肿瘤学杂志 ›› 2017, Vol. 44 ›› Issue (11): 856-859.doi: 10.3760/cma.j.issn.1673-422X.2017.11.013

• 综述 • 上一篇    下一篇

碱基切除修复及其靶向治疗策略

张天棋,王红兵   

  1. 221000 徐州医科大学研究生学院(张天棋);徐州医科大学附属医院肿瘤科(王红兵)
  • 收稿日期:2017-08-07 出版日期:2017-11-08 发布日期:2017-11-24
  • 通讯作者: 王红兵 E-mail:594466160@qq.com

Base excision repair and targeted therapy strategies

Zhang Tianqi, Wang Hongbing   

  1. Graduate School, Xuzhou Medical University, Xuzhou 221000, China
  • Received:2017-08-07 Online:2017-11-08 Published:2017-11-24
  • Contact: Wang Hongbing E-mail:594466160@qq.com

摘要: 碱基切除修复(BER)是DNA氧化损伤修复的重要通路,该通路的突变造成基因不稳定而增加癌症风险。大量研究已证明,BER通路的关键蛋白,如DNA糖基化酶、脱嘌呤/嘧啶核酸内切酶1、DNA聚合酶等,在多种肿瘤中异常表达。此外这些蛋白的单核苷酸多态性影响肿瘤细胞的修复活性,有望成为肿瘤诊断、治疗及预后评估的重要指标。

关键词: 基因修复, 多态性, 基因组不稳定性, 碱基切除修复

Abstract: Base excision repair (BER) is an important pathway for DNA oxidative damage repair, and mutations in this pathway cause gene instability and increase cancer risk. A large number of studies have shown that abnormal expression of key proteins in the BER pathway in a variety of tumors, such as DNA glycosylase, apurinic/apyrimidinic endonuclease 1, DNA polymerase and so on. Single nucleotide polymorphisms of these proteins affect the repair activity of tumor cells, and are expected to be important indicators for the diagnosis, treatment and evaluation of prognosis.

Key words: DNA repair, Polymorphism, Genomic instability, Base excision repair