Apoptosis of bladder transitional cell carcinoma T24 cells induced by adenovirus-mediated inducible nitric oxide synthase gene transfection

被引:0
|
作者
Jing Tan [1 ,2 ]
Qing Zeng [1 ,2 ]
Xian-Zheng Jiang [1 ,2 ]
Le-Ye He [1 ,2 ]
Jin-Rong Wang [1 ,2 ]
Kun Yao [1 ,2 ]
Chang-Hui Wang [1 ,2 ]
机构
[1] Department of Urology,The Third Xiangya Hospital of Central South University
[2] Department of Urology,The Third Xiangya Hospital,Yue-lu District
关键词
Bladder cancer; T24 cell line; iNOS gene; gene therapy;
D O I
暂无
中图分类号
R737.14 [膀胱肿瘤];
学科分类号
100214 ;
摘要
Objectives:To investigate the effects of adenovirus-mediated inducible nitric oxide synthase gene transfection on bladder transitional cell carcinoma T24 cells,and to provide novel insights and approaches to clinical therapies against bladder transitional cell carcinoma.Methods:Firstly,construct recombinant adenovirus vector pAd-iNOS of iNOS,followed by transfection of pAd-iNOS into HECK293 packaging cells.Thirdly,harvest recombinant adenovirus rAd-iNOS after amplification and purification procedures.Finally,transfect the recombinant adenovirus rAd-iNOS into human bladder carcinoma T24 cells and examine the effect of rAd-iNOS transfection on apoptosis of T24and possible mechanism.Results:As shown by this study,the recombinant adenovirus rAd-iNOS was constructed successfully.The virus titer was 5.8×108PFU/mL and recombinant was verified by PCR analysis.Transfection of adenovirus rAd-iNOS into T24 cells could induce secretion of high NO concentration,P53 protein expression upregulation,as well as promotion of T24 cell apoptosis.Conclusions:The transfection of human bladder carcinoma T24 cells from recombinant adenovirus rAdiNOS was confirmed to induce intracellular iNOS over-expression,high production of NO,up-regulation of intracellular P53 expression and promotion of cell apoptosis.
引用
收藏
页码:593 / 599
页数:7
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