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p16基因重组质粒的构建及其对人肺癌细胞的抑制作用
引用本文:付晓颖,曹世龙,冉瑞琼,邵东敏,张颂文,申宗候,顾建新.p16基因重组质粒的构建及其对人肺癌细胞的抑制作用[J].中国肿瘤生物治疗杂志,1998,5(1):9-12.
作者姓名:付晓颖  曹世龙  冉瑞琼  邵东敏  张颂文  申宗候  顾建新
作者单位:第二军医大学免疫学教研室!上海200433,第二军医大学免疫学教研室!上海200433,第二军医大学免疫学教研室!上海200433,河南省人民医院生物治疗中心!郑州450003,河南省人民医院生物治疗中心!郑州450003,河南省人民医院生物治疗中心!郑州450003,河南省人民医院生物治疗中心!郑州45
基金项目:自然科学基金(39600181)资助
摘    要:表达大肠杆菌胞嘧啶脱胺酶(CD)基因的重组腺病毒AdCD体外转染小鼠黑色素瘤细胞B16F10,结果显示转染了CD基因的B16F10细胞对5-氟胞嘧啶(5FC)的敏感性显著提高.将经AdCD/5FC系统处理的B16F10细胞上清倍比稀释后.加至野生型B16F10细胞中,发现当上清仅占6.25%时即可对野生型B16F10细胞发挥明显的杀伤作用,提示AdCD/5FC介导的旁观者效应可能是通过5FC经CD酶代谢产生的毒性产物扩散而实现的.本实验还观察了CD基因体内转染后的杀伤效果,荷瘤小鼠经注射AdCD并连续10天给予5FC治疗后,与PBS、对照病毒AdLacZ/5FC治疗小鼠比较,小鼠肿瘤生长明显受到抑制,小鼠存活期明显延长.

关 键 词:基因治疗  胞嘧啶脱胺酶  自杀基因  5氟胞嘧啶  腺病毒  黑色素瘤
收稿时间:8/8/1997 12:00:00 AM
修稿时间:1997/10/24 0:00:00

Construction of p16 Gene Recombinant Expression Vector and Its Antitumorigenic Effects on Human Lung Adenocarcinoma Cells
Fu Xiaoying,Cao Shilong,Ran Ruiqiong,Shao Dongmin,Zhang Songwen,Shen Zonghou and Gu Jianxin.Construction of p16 Gene Recombinant Expression Vector and Its Antitumorigenic Effects on Human Lung Adenocarcinoma Cells[J].Chinese Journal of Cancer Biotherapy,1998,5(1):9-12.
Authors:Fu Xiaoying  Cao Shilong  Ran Ruiqiong  Shao Dongmin  Zhang Songwen  Shen Zonghou and Gu Jianxin
Institution:Cancer Hospital, Shanghai Medical University, Shanghai 200032;Cancer Hospital, Shanghai Medical University, Shanghai 200032;Cancer Hospital, Shanghai Medical University, Shanghai 200032;Cancer Hospital, Shanghai Medical University, Shanghai 200032;Cancer Hospital, Shanghai Medical University, Shanghai 200032;Cancer Hospital, Shanghai Medical University, Shanghai 200032;Cancer Hospital, Shanghai Medical University, Shanghai 200032
Abstract:Escherichia coli cytosine deaminase ( CD) gene was transfected into murine B16F10 melanoma cells by recombinant adenovirus AdCD in vitro . The tumor cells infected with AdCD were more sensitive to 5-fluorocytosine (5FC) than cells infected with a control adenovirus AdLacZ. The supernatant from B16F10 cells treated with AdCD/5FC was transferred to uninfected cells, and we found that only 6. 25 % of the supernatant could significantly inhibit the growth of wild type B16F10 cells. When AdCD was directly injected into established subcutaneous B16F10 tumors in mice followed by intraperitoneal injection of 5FC for 10 days, a significant reduction in tumor size and prolongation of survival period were observed. These studies not only explored the cytotoxic effects of AdCD/5FC on B16F10 melanoma cells in vitro and in vivo but also elucidated the mechanisms of its bvstander effect.
Keywords:gene therapy  cytosine deaminase  suicide gene  5-fluorocytosine  melanoma  adenovirus
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