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作 者:臧光祥[1] 孙宏晨[1] 穆亚冰[1] 张泽兵[1] 柯小亮[1] 刘金钟[1] 苏涛[2]
机构地区:[1]吉林大学口腔医学院病理科,吉林长春130041 [2]湖州师范学院医学院
出 处:《口腔医学研究》2007年第5期481-484,共4页Journal of Oral Science Research
基 金:国家自然基金(编号:30672338);吉林省国际合作基金(编号:20050702-6)
摘 要:目的:探讨以凋亡基因TRAIL为靶基因,腺病毒(Ad)为载体,人端粒酶(TERT)启动子引导的重组基因治疗药物AdTERT-TRAIL诱导人鳞状细胞癌细胞(TCa8113)凋亡的作用。方法:含有绿色荧光蛋白基因(EGFP)的腺病毒载体(AdTERT-EGFP)转染TCa8113细胞,确定重组腺病毒载体转染效率;AdTERT-EGFP为对照组,AdTERT-TRAIL为实验组感染TCa8113细胞,采用RT-PCR方法检测TRAIL的表达。应用倒置显微镜观察细胞形态,应用MTT检测细胞的存活率,流式细胞仪检测细胞凋亡率。结果:AdTERT-EGFP在1000p/cell时转染效率为100%。RT-PCR可检测到594bp的TRAIL基因。细胞转染AdTERT-TRAIL和AdTERT-EGFP后,随时间细胞存活率逐渐下降,但AdTERT-TRAIL组较AdTERT-EGFP组下降更快,统计学分析有显著意义(P<0.001)。AdTERT-TRAIL和AdTERT-EGFP均能诱导TCa8113细胞凋亡,而AdTERT-TRAIL组引起细胞凋亡的程度明显比AdTERT-EGFP组大,统计学有显著差异(P<0.0001)。结论:AdTERT-TRAIL在体外能明显抑制TCa8113细胞的活性,并能促进其凋亡。Objective:To study the apoptotic effect on the squamous cell carcinoma cell line TCa8113 induced by recombined adenovirus vector containing TRAIL gene and TERT promoter.Methods:The TCa8113 cell line was firstly infected with AdTERT-EGFP containing enhanced green fluorescence protein gene(EGFP),in order to obtain the definite titre of this adenovirus vector.Then,the TCa8113 cell line was infected with AdTERT-TRAIL,and the expression of TRAIL gene was detected by means of RT-PCR,the activity of TCa8113 cell line was evaluated by MTT and the apoptosis were detected by flow cytometer.Results:The proper titre was 1000p/cell,and TCa8113 cell line could be infected 100% in this titre.TRAIL gene was detected by RT-PCR after the cells were infected with AdTERT-TRAIL.The activity of TCa8113 decreased in both groups,but the AdTERT-TRAIL group decreased more sharply than AdTERT-EGFP group,the statistic analysis is significant(P〈0.001).Both AdTERT-TRAIL and AdTERT-EGFP could lead to apoptosis of TCa8113 cells,but the AdTERT-TRAIL function more efficiently than AdTERT-EGFP.Especially there was remarkable statistic difference between two groups(P〈0.001).Conclusion:AdTERT-TRAIL could effectively decrease the activity of TCa8113 cells and induce apoptosis.
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