ZHANG Ronggui, et al. Suicide gene therapy for mouse bladder cancer using HSV-tk/GCV system[J]. Journal of Chongqing Medical University, 2005,(4):513-515.
ZHANG Ronggui, et al. Suicide gene therapy for mouse bladder cancer using HSV-tk/GCV system[J]. Journal of Chongqing Medical University, 2005,(4):513-515. DOI: 10.13406/j.cnki.cyxb.2005.04.008.
目的:在体外和体内水平建立膀胱癌的单纯疱疹病毒-胸苷激酶/丙氧鸟苷(herpes simplex virus type thymidine Ki-nase/ganciclovir
HSV-tk/GCV)自杀基因系统
并验证该系统的有效性。方法:用逆转录病毒载体HSV-TK转染鼠膀胱癌细胞株T739
体外检测其对GCV的敏感性
在同基因鼠
分别建立T739和T739-TK膀胱癌腹腔肿瘤模型。当B超显示肿瘤直径约0.5
0
.8cm时
腹腔GCV给药6天
然后观察肿瘤大小变化及动物存活时间。结果:GCV对T739-TK细胞有显著杀伤作用
而对T739细胞的生长无影响
成功的建立了T739同基因鼠膀胱癌腹腔肿瘤模型
体内实验得到相应结果
转染了TK基因的T739鼠肿瘤明显变小
甚至消失
而未转染TK基因的T739鼠肿瘤继续增大
GCV对其无明显治疗作用
转染了TK基因的T739鼠存活时间显著延长。结论:在体外和体内水平
表达TK基因的肿瘤细胞均被GCV有效杀伤
这表明HSV-tk/GCV系统有可能成为基因治疗膀胱癌的有效方法。
Abstract
Objective:To establish a suicide gene therapy system HSV-tk/GCV for bladder cancer
a treatment in vitro as well as in vivo and to test its efficacy.Methods:Mouse bladder cancer cell line (T739) was transfected with retroviral vector HSV-tk gene.The sensitivity of T739-TK cells to GCV was detected in vitro.In the mouse model of bladder tumor
T739 or T739-TK was implanted beneath the peritoneum of syngeneic mice.When tumors grew to the size of 0.5~0.8cm
intraperitoneal administration of GCV was carried out for 6 days.Changes of tumor size and survival rate of mice were observed.Results:RT-PCR showed that TK gene was transferred into the T739 cell and expressed successfully. In vitro
T739-TK cells became sensitive to low concentrations of GCV.In vivo studies showed similar result.Significant tumor inhibition was found in the T739-TK group after administration of GCV
and the survival time of mice was prolonged.Conclusion:Tumor cells expressing HSV-tk gene were eradicated by administration of GCV in vitro as well as in vivo.