首页 | 本学科首页   官方微博 | 高级检索  
     

腺病毒介导多基因在胆管癌细胞中的表达
引用本文:王征旭,何振平,吴祖泽,马宽生,刘吉奎,张维维. 腺病毒介导多基因在胆管癌细胞中的表达[J]. 第三军医大学学报, 1999, 21(10): 742-745
作者姓名:王征旭  何振平  吴祖泽  马宽生  刘吉奎  张维维
作者单位:1. 第二军医大学东方肝胆外科医院,上海,200438
2. 第三军医大学附属西南医院肝胆外科中心,重庆,400038
3. 军事医学科学院放射医学研究所百环生物医学研究中心,北京,100000
4. 美国Baxter医疗用品公司基因治疗部
摘    要:研究腺病毒介导的多基因(GM-CSF,B7-1,p53、IL-2)在胆管癌细胞系QBC939中的表达及对其生长的影响。方法:构建同时含GM-CSF、B7-1、p53、IL-2 4种目的基因的重组腺病毒载体Ad-multigenes,应用流式细胞仪、ELISA、免疫组化等方法。

关 键 词:多基因腺病毒  胆管癌细胞系  基因表达  生长抑制

Expression of adenovirus-mediated GM-CSF, B7-1, p53 and IL-2 in cholangiocarcinoma cells line
Wang Zhengxu,He Zhengping,Wu Zuze,Ma Kuansheng,Liu Jikui,Zhang Weiwei. Expression of adenovirus-mediated GM-CSF, B7-1, p53 and IL-2 in cholangiocarcinoma cells line[J]. Acta Academiae Medicinae Militaris Tertiae, 1999, 21(10): 742-745
Authors:Wang Zhengxu  He Zhengping  Wu Zuze  Ma Kuansheng  Liu Jikui  Zhang Weiwei
Affiliation:Wang Zhengxu, He Zhengping, WuZuze, Ma Kuansheng, Liu Jikui, Zhang Weiwei (Department of Hepatobiliary Surgery,Southwest Hospital, Third Military Medical University,Chongqing,400038)
Abstract:Objective: To study the expression rate of adenovirus-mediated human genes of GM-CSF,B7-1, p53 and IL-2 in the cells of cholangiocarcinoma cell line QBC939 and their effects on the growth of the malignant cells. Methods: Recombinant adenovirus was constructed to contain human genes of GM-CSF,B7-1, p53 and IL-2 and the expression rate of the genes in the ce1ls of hurnan cholangiocarcinoma celI line QBC939 was detected with ELISA, immunohistochemistry and FACS. In addition, the growth of the malignant cells was deIineated. ResuIts: Adenovirus-mediated multigenes except IL-2 were expressed in high rate in the malignant cells and they inhibited the growth of the cells. Conclusion: Adenovirus-mediated human genes of GM-CSF, B7-1 and p53 can be expressed in cholangiocarcinoma cell line QBC939 and inhibit the growth of the cells.
Keywords:GM-CSF  B7-1  p53  IL-2  cholangiocarcinoma cell line  gene expression  growth inhibition
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