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Ad-p53与Ad-p16联合对人肺腺癌GLC-82细胞作用的体外实验研究 *
引用本文:徐敏毅,林 晨,梁 萧,付 明,张雪艳,吴旻.Ad-p53与Ad-p16联合对人肺腺癌GLC-82细胞作用的体外实验研究 *[J].中国肿瘤生物治疗杂志,2000,7(2):86-89.
作者姓名:徐敏毅  林 晨  梁 萧  付 明  张雪艳  吴旻
作者单位: 
基金项目:* 本课题受863计划项目(Z20-01-02)资助
摘    要:探讨腺病毒介导的p53与p16基因的联合对人肺腺病GLC-82疗效提高的可能性。方法:将分别携有p53基因、p16基因重组腺病毒(Ad-p53与Ad-p16)联合使用,通过细胞生长和存活实验、克隆形成实验、流式细胞分析、TUNEL检测、RT-PCR分析、免疫组织化学实验,观察其对人肺腺癌GLC-82细胞的作用。结果:在总感染强度相同的前提下,Ad-p53与Ad-p16联合导入GLC-82细胞,对细胞生长存活及克隆形成能力的抑制、以及所造成的凋亡效果比施用单种基因的效果强,表明p53基因与p16基因在体外疗效上互为协同。结论: Ad-p53与Ad-p16联合,可以提高对人肺腺癌GLC-82细胞的疗效。

关 键 词:肿瘤基因治疗    联合治疗
收稿时间:1999/8/11 0:00:00
修稿时间:1999/11/29 0:00:00

The Experimental Studies of Ad-p53 and Ad-p16 in Combination on Human Lung Adenocarcinoma Cell Line GLC-82
Xu Minyi,Lin Chen,Liang Xiao,Fu Ming,Zhang Xueyan and Wu Min.The Experimental Studies of Ad-p53 and Ad-p16 in Combination on Human Lung Adenocarcinoma Cell Line GLC-82[J].Chinese Journal of Cancer Biotherapy,2000,7(2):86-89.
Authors:Xu Minyi  Lin Chen  Liang Xiao  Fu Ming  Zhang Xueyan and Wu Min
Institution:National Laboratory of Molecular Oncology, Cancer Institute, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100021;National Laboratory of Molecular Oncology, Cancer Institute, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100021;National Laboratory of Molecular Oncology, Cancer Institute, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100021;National Laboratory of Molecular Oncology, Cancer Institute, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100021;National Laboratory of Molecular Oncology, Cancer Institute, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100021;National Laboratory of Molecular Oncology, Cancer Institute, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100021
Abstract:To determine the effect of Ad-53 and Ad-16both alone and in combination on the growth of human lung adeuocarcinoma cell line GLC-82. Methods: Human lung adenocarcinoma cell line GLC-82 were trasferredvia an adenovirus-mediated p53 gene (Ad-p53), P16 gene Ad-p16 or both. Cell growth inhibition assay, colony formation, flow cytometry assay, TUNEL, RT-PCR and immunhistochemistry assays were used to evaluate the therapeutic efficiency of such strategy on trasferred cells. Results: in vitro experiments, at the same dose ofAd (multiplicity of infection), simultaneous transfer of Ad-p53 and Ad-p16 to GLC-82 cells caused stronger therapeutic efficacy than caused by single kind of Ad transfer, demonstrating that Ad-p53 treatment has synergistic efficacy with Ad-p16 treatment on GLC-82 cells. Conclusion: Ad-p53 for GLC-82 cells shows enhanced therapeutic efficiency when combined with Ad-p16.
Keywords:cancer gene therapy  combined therapy
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