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整合素靶向性病毒载体对肿瘤细胞基因转导的促进作用
引用本文:高建青,陈海靓,中川晋作,水口裕之,梁文权. 整合素靶向性病毒载体对肿瘤细胞基因转导的促进作用[J]. 药学学报, 2006, 41(11): 1116-1120
作者姓名:高建青  陈海靓  中川晋作  水口裕之  梁文权
作者单位:1. 浙江大学,药物制剂研究所,浙江,杭州,310031
2. 日本大阪大学,药学研究科,日本,大阪,565-0871
3. 日本国立生物医学创新研究所,日本,大阪,567-0085
摘    要:在进行基因导入研究及临床试验中,目前采用的载体通常包括了病毒及非病毒两大类。对于非病毒载体用于基因转染有许多报道。而腺病毒作为基因载体,因其具有的高效转导能力及对分裂或非分裂细胞均能转导等优点而被广泛应用于针对疾病的基因治疗中。对腺病毒进入细胞机制进行的深入研究结果发现,腺病毒与细胞结合的第一步是与细胞表面的柯萨奇腺病毒受体(coxsackie adenovirus receptor,CAR)结合,第二步是利用其在五角体基(pentonbase)中的RGD序列和细胞表面的整合素结合,

关 键 词:重组腺病毒  肿瘤细胞  基因表达  整合素
文章编号:0513-4870(2006)11-1116-05
收稿时间:2006-01-05
修稿时间:2006-01-05

Gene expression of tumor cells both in vitro and in vivo enhanced by integrin-targeting adenovirus vector
GAO Jian-qing,CHEN Hai-liang,NAKAGAWA Shinsaku,MIZUGUCHI Hiroyuki,LIANG Wen-quan. Gene expression of tumor cells both in vitro and in vivo enhanced by integrin-targeting adenovirus vector[J]. Acta pharmaceutica Sinica, 2006, 41(11): 1116-1120
Authors:GAO Jian-qing  CHEN Hai-liang  NAKAGAWA Shinsaku  MIZUGUCHI Hiroyuki  LIANG Wen-quan
Affiliation:1. Institute of Pharmaceutics, Zhejiang University, Hangzhou 310031, China ; 2. Graduate School of Pharmaceutical Sciences, Osaka University, suita 565-0871, Japan ; 3. National Institute of Biomedical Innovation, Osaka 567-0085, Japan
Abstract:Aim To construct an efficient recombinant viral vector for gene therapy.Methods(First-generation) adenovirus(Ad) vector was modified with the RGD peptide inserted into the fiber.Both in vitro and in vivo experiments of gene expression in different tumor cells with conventional and recombinant vectors were conducted.RT-PCR was used for detecting the expression of coxackievirus and adenovirus receptor and integrin at the surface of Meth-A cells.Results Fiber-mutant adenovirus vector showed a notably enhanced gene expression in A2058,B16BL6,OV-HM,and Meth-A tumor cells compared with that of conventional ones.In vivo study carried out using Meth-A tumor-bearing mice also demonstrated that the intra-tumoral injection of recombinant adenovirus induced strong gene expression in these CAR-deficient tumor cells. Conclusion The recombinant vector can be a promising one for effective cancer gene therapy.
Keywords:recombinant adenovirus vector   tumor cell   gene expression   integrin
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