癌变·畸变·突变 ›› 2019, Vol. 31 ›› Issue (3): 203-207.doi: 10.3969/j.issn.1004-616x.2019.03.006

• 论著 • 上一篇    下一篇

氟达拉滨与TRAIL联用诱导肺癌细胞凋亡及其作用机制

王子依1,2, 张露露2, 孙震晓1, 刘长振2   

  1. 1. 北京中医药大学生命科学学院, 北京 100029;
    2. 中国中医科学院医学实验中心, 中医药防治重大疾病基础研究北京重点实验室, 北京 100700
  • 收稿日期:2019-03-01 修回日期:2019-05-05 出版日期:2019-05-31 发布日期:2019-05-31
  • 通讯作者: 刘长振,Email:lcz0220@163.com;孙震晓,E-mail:sunzxcn@hotmail.com E-mail:lcz0220@163.com;sunzxcn@hotmail.com
  • 作者简介:王子依,E-mail:875103325@qq.com。
  • 基金资助:
    国家自然科学基金项目(31170829,81171762,81550017,81473418);北京市自然科学基金资助项目(7172150);中国中医科学院自主选题项目(ZZ2015015)

Fludarabine combined with TRAIL induced apoptosis in lung cancer A549 cells

WANG Ziyi1,2, ZHANG Lulu2, SUN Zhenxiao1, LIU Changzhen2   

  1. 1. School of Life Science, Beijing University of Chinese Medicine, Beijing 100029;
    2. Beijing Key Laboratory of Chinese Medicine on Prevention and Treatment for Major Disease Experimental Research Center, China Academy of Chinese Medical Sciences, Beijing 100700, China
  • Received:2019-03-01 Revised:2019-05-05 Online:2019-05-31 Published:2019-05-31

摘要: 目的:研究氟达拉滨(Fludarabine)在低浓度下与TRAIL联合处理是否能够诱导人肺癌A549细胞发生凋亡,并探讨其作用机制。方法:实验设对照组、Fludarabine组、TRAIL组、Fludarabine和TRAIL联合组,CCK-8法检测Fludarabine与TRAIL联合处理时对A549细胞及人脐静脉内皮细胞(HUVEC,人正常细胞作为对照)增殖活力的影响,流式细胞术检测A549细胞凋亡情况,Western blot法检测凋亡相关蛋白Survivin、Bcl-2、Bcl-xl、caspase-8、caspase-3、JNK和p38的表达情况。结果:25、50 μmol/LFludarabine或50 ng/mL TRAIL单独处理时对A549及HUVEC细胞增殖活力均无明显影响(P均>0.05),两者联合处理后对A549细胞增殖活力抑制率分别为30.9%和44.9%。Fludarabine或TRAIL单独使用时对A549细胞凋亡无明显影响,联合处理时可使A549细胞凋亡率达到89.3%。与对照组、Fludarabine组和TRAIL组相比,Fludarabine与TRAIL联合处理可使A549细胞中Survivin、Bcl-2、Bcl-xl表达降低(P均<0.05),促进caspase-8及caspase-3的激活,并能促进JNK和p38的磷酸化(P均>0.05)。结论:Fludarabine与TRAIL联合处理可促进A549细胞凋亡。

关键词: 氟达拉滨, 肿瘤坏死因子相关凋亡诱导配体, A549, 细胞凋亡

Abstract: OBJECTIVE:This study aimed to investigate whether Fludarabine,at a low-concentration, would enhance induction of apoptosis in A549 cells by TRAIL. METHODS: A549 cultures were organized into different groups:control, Fludarabine, TRAIL, and Fludarabine plus TRAIL. The CCK-8 method was used to detect effect of Fludarabine and/or TRAIL on A549 and human umbilical vein endothelial cells (HUVEC). Flow cytometry was used to detect apoptosis rates. Western Blot was used to detect apoptosis-related proteins Survivin,Bcl-2,Bcl-xl,caspase-8,caspase-3,and the expression of JNK and p38. RESULTS: Fludarabine(25 or 50 μmol/L) or TRAIL alone had no significant effects on viability of A549 and HUVEC cells, or apoptosis in A540 cells. The inhibition rates from combined treatment of Fludarabine (25 or 50 μmol/L) and TRAIL were 30.9% and 44.9%, respectively, in A549 cells and the effect was concentration dependent. The combined treatment also caused apoptosis in 89.3% of A549 cells, as well as decreased expression of Survivin,Bcl-2 and Bcl-xl,promoted the activation of caspase-8 and caspase-3,and promoted the phosphorylation of JNK and p38. CONCLUSION:Fludarabine combined with TRAIL specifically induced apoptosis in A549 cells.

Key words: Fludarabine, tumor necrosis factor-related apoptosis-inducing ligand, A549, apoptosis

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