betway必威登陆网址 (betway.com )学报››2022,Vol. 43››Issue (10): 788-791.DOI:10.3969/j.issn.2097-0005.2022.10.013

• 综述 •上一篇下一篇

BIM缺失与非小细胞肺癌患者抗肿瘤治疗研究进展

张岱1,2(), 李炫宗2, 黄彩梅3, 王琳琳1,2()

  1. 1.山东大学, 山东 济南 250012
    2.山东省肿瘤医院, 山东 济南 250117
    3.betway必威登陆网址 (betway.com ), 山东 济南 250117
  • 收稿日期:2022-04-15出版日期:2022-10-25发布日期:2022-11-19
  • 通讯作者:王琳琳
  • 作者简介:张岱,硕士研究生,研究方向:肿瘤学,E-mail:zhangdai07@163.com。。

Research progress of BIM deletion polymorphism and anti-tumor therapy in NSCLC patients

Dai ZHANG1,2(), Xuanzong LI2, Caimei HUANG3, Linlin WANG1,2()

  1. 1.Shandong University,Jinan 250012,China
    2.Shandong Cancer Hospital,Jinan 250117,China
    3.Shandong First Medical University & Shandong Academy of Medical Sciences,Jinan 250117,China
  • Received:2022-04-15Online:2022-10-25Published:2022-11-19
  • Contact:Linlin WANG

摘要:

BIM属于Bcl‐2家族,是促进细胞凋亡的关键因子。BIM缺失能导致促凋亡结构域BH3缺失,从而阻碍细胞凋亡。已有研究报道,BIM缺失及表达下降可能引起患者对肿瘤治疗的抵抗。本文旨在对BIM缺失与非小细胞肺癌(non?small cell lung cancer, NSCLC)治疗疗效的关系相关进展进行综述。

关键词:非小细胞肺癌,BIM缺失,抗肿瘤治疗,凋亡

Abstract:

BIM belongs to bcl-2 family and is a key factor promoting apoptosis. Loss of BIM can lead to loss of the pro-apoptotic domain BH3, thus inhibiting apoptosis. It has been reported that the loss and decreased expression of BIM may lead to the resistance of patients to tumor therapy. This article aims to review the relationship between BIM deletion polymorphism and therapeutic efficacy of non-small cell lung cancer (NSCLC).

Key words:non?small cell lung cancer,BIM deletion polymorphism,antitumor therapy,apoptosis