J4 ›› 2011, Vol. 37 ›› Issue (4): 571-576.

• 基础研究 •    下一篇

Smac过表达增强氯化镉对人肝癌细胞SMMC-7721的增殖抑制和促凋亡作用

 郭彩霞, 李艳博, 王斌, 于洋, 于永波, 段军超, 孙志伟   

  1. (首都医科大学公共卫生与家庭医学学院|北京 100069)
  • 收稿日期:2011-03-22 出版日期:2011-07-28 发布日期:2011-07-28
  • 通讯作者: 孙志伟 E-mail:Tel:010-83911507,E-mail:zwsun@ccmu.edu.cn);
  • 作者简介:郭彩霞(1981-)|女|山西省平遥县人|讲师|医学博士|主要从事肿瘤治疗和毒理学安全性评价方面的研究。
  • 基金资助:

    国家自然科学基金青年基金资助课题(30700672)

Enhancement of antiproliferative and proapoptotic effects of cadmium chloride when coupling with Smac over-expression in hepatocellular carcinoma cells

 GUO Cai-Xia, LI Yan-Bo, WANG Bin, YU Yiang, YU Yong-Bei, DUAN Jun-Chao, SUN Zhi-Wei   

  1. (School of Public Health and Family Medicine,Capital Medical University,Beijing 100069,China)  
  • Received:2011-03-22 Online:2011-07-28 Published:2011-07-28

摘要:

目的:研究Smac过表达联合氯化镉(CdCl2)对人肝癌细胞SMMC-7721增殖和凋亡的影响,为以Smac为基础的肿瘤基因治疗以及镉作为抗肝癌药物的开发提供实验依据。方法:实验共设立5组,分别为对照组、pcDNA3.1+组、pcDNA3.1+-hSmac组、CdCl2组以及CdCl2联合Smac组。对照组细胞不进行细胞转染、不染毒;pcDNA3.1+和pcDNA3.1+-hSmac组细胞采用脂质体介导的方法分别转染空载体pcDNA3.1+和携带Smac基因的重组质粒pcDNA3.1+-hSmac;CdCl2组给予不同浓度(10、20和30  μmol·L-1)CdCl2;CdCl2联合Smac组细胞首先将pcDNA3.1+-hSmac转染入SMMC-7721,然后给予CdCl2处理。采用MTT法检测Smac过表达联合CdCl2对细胞增殖的影响,AO/EB法和Annexin Ⅴ/PI双荧光标记流式细胞术(FCM)检测细胞凋亡。 结果:MTT结果显示,与对照组比较,除空载体pcDNA3.1+组无统计学意义外,其余各组细胞A490值均降低,抑制率均明显增加,差异具有统计学意义(P<0.01或P<0.001);单纯CdCl2组细胞抑制率随剂量增加而显著上升;分别与相应的单纯CdCl2组和pcDNA3.1+-hSmac组比较,CdCl2联合Smac组细胞的抑制率明显升高(P<0.001)。AO/EB染色荧光显微镜下观察显示,对照组细胞状态良好,而pcDNA3.1+-hSmac组、30  μmol·L-1 CdCl2组及CdCl2联合Smac组细胞出现凋亡形态学改变,且后者最为明显。FCM结果显示,pcDNA3.1+-hSmac组细胞凋亡率增加,分别与对照组和pcDNA3.1+组比较,差异均具有统计学意义(P<0.001)。CdCl2联合Smac组细胞凋亡率最高,显著高于单纯30  μmol·L-1 CdCl2组(P<0.001)。结论:CdCl2对SMMC-7721细胞具有毒性,可抑制细胞增殖,呈现剂量-效应系,可诱导细胞凋亡。Smac过表达可抑制SMMC-7721细胞增殖,诱导细胞凋亡,并可增强CdCl2对SMMC-7721细胞的增殖抑制和促凋亡作用。

关键词: 氯化镉;Smac;凋亡;增殖;肝肿瘤;SMMC-7721

Abstract:

Abstract:Objective
To study the effects of the cotreatment of cadmium chloride (CdCl2) and Smac over-expression on proliferation and apoptosis of hepatocellular carcinoma cells,SMMC-7721,and provide an experimental basis for the Smac-based tumor gene therapy and the development of cadmium as the antihepatoma drug.Methods SMMC-7721 were divided into five groups,which were control,pcDNA3.1+,pcDNA3.1+-hSmac,single CdCl2-treated and CdCl2 plus Smac groups respectively. The cells in control group had no transfection or CdCl2 treatment,while those in pcDNA3.1+ and pcDNA3.1+-hSmac groups were transfected with null vector pcDNA3.1+ or pcDNA3.1+-hSmac respectively through lipofectamine-mediated method,and those in CdCl2-treated groups were exposed to CdCl2 at the concentration of 10,20 and 30  μmol·L-1 respectively,and those in CdCl2 plus Smac groups were transfected with pcDNA3.1+-hSmac firstly,and then treated with CdCl2 after transfection for 24 h.MTT assay was used to determine the effect of Smac over-expression and CdCl2 on proliferation,and both AO/EB fluorescence staining and FCM with Annexin Ⅴ and PI double-staining methods for apoptosis.Results The  MTT results showed that compared with control group,except for  the null-vector pcDNA3.1+ group,the inhibitory rates in the rest groups were increased significantly (P<0.01 or P<0.001).In  single CdCl2-treated groups,the inhibitory rate was increased with the increasing of treatment doses,whereas,each Smac coupled group presented significantly higher inhibitory rate than the corresponding single CdCl2-treated group (P<0.001).AO/EB staining manifested that the  cells in control group were in good condition,while those in pcDNA3.1+-hSmac,30  μmol·L-1 CdCl2 treatment,and CdCl2 plus Smac groups appeared the  morphological changes of apoptosis,especially in the last group.Furthermore,the results acquired by FCM showed that the apoptotic rate in pcDNA3.1+-hSmac group was increased significantly when compared with control and pcDNA3.1+ groups respectively (P<0.001).However,the apoptotic rate in CdCl2 pluse Smac group was the highest,which was significantly higher than that in single 30  μmol·L-1 CdCl2-treated group (P<0.001).Conclusion CdCl2 has cytotoxicity to SMMC-7721 cells.It could inhibit cellular proliferation in a dose-dependent manner,and induce apoptosis.Smac over-expression  could inhibit cellular proliferation and slightly induce apoptosis independently.

Key words: cadmium chloride;Smac;apoptosis;proliferation;liver neoplasms;SMMC-7721

中图分类号: 

  • R994.6