首页 | 本学科首页   官方微博 | 高级检索  
检索        

肿瘤坏死因子相关配体与阿司匹林合用对肝癌SMMC-7721细胞凋亡的影响
引用本文:李小安,房殿春,司佩任,张汝刚,杨柳芹.肿瘤坏死因子相关配体与阿司匹林合用对肝癌SMMC-7721细胞凋亡的影响[J].中华肝脏病杂志,2003,11(11):676-679.
作者姓名:李小安  房殿春  司佩任  张汝刚  杨柳芹
作者单位:400038,重庆,第三军医大学西南医院全军消化专科中心
基金项目:全军“十五”科研基金资助项目(01MA172)
摘    要:目的 观察肿瘤坏死因子相关的凋亡诱导配体(TRAIL)与阿司匹林合用对肝癌SMMC-772l细胞的作用。方法 氨甲喋呤法检测SMMC-772l细胞存活分数;流式细胞仪检测SMMC-772l细胞的凋亡率和细胞周期;WesternBlot法检测凋亡相关基因的表达。结果 单用300ng/ml TRAIL、3、10mmol/L阿司匹林SMMC-772l细胞存活分数分别为82.76%、81.34%和71.29%,合用的存活分数分别为43.5%、37.8%。3、l0mmol/L阿司匹林与300ng/ml TRAIL合用诱导的细胞凋亡率明显大于单用两药诱导的细胞凋亡率之和(单用300ng/ml TRAIL、3mmol/L和10mmol/L阿司匹林凋亡率分别为21.25%、1.89%和6.08%,合用的凋亡率分别34.76%,38.56%)并使G0/Gl期细胞增加l3、10mmol/L的阿司匹林使SMMC-772l细胞Bcl-2的表达明显减弱,但对Bax的表达无影响。结论 TRAlL与阿司匹林合用对肝癌SMMC-772l细胞有明显的协同杀伤作用,其机制可能与阿司匹林抑制Bcl-2的表达有关。

关 键 词:肿瘤坏死因子  阿司匹林  肝癌  SMMC-772l细胞  细胞凋亡  凋亡诱导配体
修稿时间:2002年11月12

Cooperative anti-tumor effect of aspirin and TNF-related apoptosis-inducing ligand
LI Xiao-an,FANG Dian-chun,SI Pei-ren,ZHANG Ru-gang,YANG Liu-qin.Cooperative anti-tumor effect of aspirin and TNF-related apoptosis-inducing ligand[J].Chinese Journal of Hepatology,2003,11(11):676-679.
Authors:LI Xiao-an  FANG Dian-chun  SI Pei-ren  ZHANG Ru-gang  YANG Liu-qin
Institution:Department of Gastroenterology, Southwest Hospital, Third Military Medical University, Chongqing 400038, China.
Abstract:Objective To observe the anti-tumor effect of combination TNF-related apoptosis-inducing ligand (TRAIL) with aspirin on liver cancer cell line, SMMC-7721. Methods The survival fraction of SMMC-7721 cells was measured by MTT assay, apoptosis rate and cell cycle was determined by flow cytometry, and the expression of apoptosis-related gene was identified by western blot. Results The survival fraction of SMMC-7721 cells treated with 300 ng/ml TRAIL, 3 mmol/L or 10 mmol/L aspirin alone was 82.76%, 81.34% and 71.29% respectively, and the survival fractions of SMMC-7721 cells treated with TRAIL and 3 mmol/L or 10 mmol/L aspirin were 43.54% and 37.8% respectively. The apoptosis rates of SMMC-7721 cells induced by TRAIL and 3 mmol/L or10 mmol/L aspirin were higher than that induced by TRAIL or aspirin alone (34.76% and 38.56% vs 21.25%, 1.89% and 6.08%), and G0/G1 arrest was observed under TRAIL and aspirin. The expression of Bcl-2 in SMMC-7721 cells treated by 3 mmol/L or 10 mmol/L aspirin decreased markedly, but no effect on Bax. Conclusion The cooperative anti-tumor effect of aspirin and TRAIL may be related to the inhibition of the expression of Bcl-2 by aspirin.
Keywords:Carcinoma  hepatocellular  TNF-related apoptosis-inducing ligand  Aspirin  Apoptosis-related gene
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号