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构建fas基因真核表达载体逆转胃癌耐药细胞MDR表型
http://www.100md.com 1999年4月15日 《世界华人消化杂志》 1999年第4期
fas基因;基因转导;多药耐药性;胃肿瘤,项目负责人,Correspondenceto,ConstructionofeukaryoticexpressionvectorpBK-fasandMDRreversaltestofdrug-resistantgastriccancercells,,Abstract,,AIM,METHODS,RESULTS,CONCLUS
     第四军医大学西京医院消化疾病研究所 陕西省西安市 710033

    时永全,男,1973-11-03生,河南省上蔡县人,汉族. 1996年第四军医大学毕业,医学学士,现为西京医院消化内科硕士研究生,研究肿瘤相关基因的克隆与肿瘤基因治疗.

    项目负责人
樊代明,710033,陕西省西安市,第四军医大学西京医院消化疾病研究所.

    Correspondence to
Dai-Ming Fan, Institute of Digestive Diseases, Xijing Hospital, 15 Changle West Road, Xi'an 710033,Shaanxi Province, China

    Tel. +86·29·3375229

    收稿日期 1998-11-26

    

    Construction of eukaryotic expression vector pBK-fas and MDR reversal test of drug-resistant gastric cancer cells


    Yong-Quan Shi, Bing Xiao, Ji-Yan Miao, Yan-Qiu Zhao, Han You and Dai-Ming Fan

    Institute of Digestive Diseases, Xijing Hospital, 15 Changle West Road, Xi'an 710033, Shaanxi Province, China

    


    Abstract

    AIM To get fas overexpressing drug-resistant gastric cancer cells by gene transduction, to compare the expressing level of fas in gene transfected and non-transfected cells, and to observe drug sensitizing effect of fas gene in transfected cells.

    METHODS
With molecular cloning technique, the full length cDNA of fas was inserted into the multiple cloning site of the expressing vector pBK-CMV. Drug-resistant gastric cancer cell strain SGC7901/VCR was transpected with recombinant plasmids, and positive clones were selected by G418. Then the expressing levels of fas gene was determined by means of Northern blot and Western blot, and MTT assay was used to detect drug sensitivity of gene transfected cells. ......

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