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机构地区:[1]广州医学院第二附属医院泌尿外科,510260 [2]武警广东总队医院内二科 [3]天津医科大学第二医院泌尿外科天津市泌尿外科研究所
出 处:《中华实验外科杂志》2009年第10期1244-1246,共3页Chinese Journal of Experimental Surgery
基 金:广州医学院第二附属医院博士启动基金资助项目(2008-2);天津市重大科技攻关计划资助项目(06YFSZSF03900)
摘 要:目的观察基因重组腺相关病毒自杀基因及内皮抑素(ES)联合基因体外治疗膀胱癌的效果。方法(1)通过基因重组腺相关病毒(rAAV)-增强绿色荧光蛋白(EGFP)转染膀胱肿瘤T24细胞,确定rAAV对T24细胞的转染效率;(2)通过rAAV-胸苷激酶(TK)-核糖体插入位点(IRES)-ES(简称rAAV—TIE)体外转染T24、HUVEC细胞,MTT法、流式细胞仪等方法来检测诱导凋亡作用。结果(1)rAAV—EGFP转染T24细胞后可以表达携带的外源基因EGFP,感染效率约为62%;(2)rAAV—TK、rAAV—TIE转染T24细胞72h后,流式细胞仪检测结果显示,rAAV—TK、rAAV—TIE两组凋亡率分别是37.02%和32.14%,明显高于空病毒转染组(7.90%)和空白对照组(0.30%)。结论rAAV—TIE可有效抑制膀胱癌的血管生成和肿瘤的生长,能够双靶点基因治疗膀胱肿瘤。Objective To investigate the effect of double targeting gene therapy by using recombinant adeno-associated virus-thymidine kinase (TK)-internal ribosome entry site (IRES)-endostatin (ES) (rAAV-TIE) in vitro. Methods ( 1 ) Bladder cancer cells of T24 were cultured and transfected by rAAV-EGFP, and the virus transfect efficacy was determined. (2) T24 and HUVEC were cultured and transfected by rAAV-ES, rAAV-MCS (blank virus) , and rAAV-TIE respectively. Seventy-two h later the levels of ES in the supernatants were measured by ELISA, and annexin V apoptosis test kit was used to examine the apoptosis. Results ( 1 ) Seventy-two h after transfection, ES could be detected in the supernatants of the T24 ceils transfected with rAAV-ES,and rAAV-TIE. (2) The apoptosis rate of the T24 cells transfected with rAAV-TK and rAAV-TIE was 34.12% and 36.91% respectively,significantly higher than that of the T24 ceils transfected with rAAV-MCS and of the control group (3.08% and 0.84% ,all P 〈 0.05). Conclusion rAAV-TIE inhibits the tumorigenesis and angiogenesis in bladder cancer effectively. Double targeting gene therapy against bladder cancer can be achieved by using rAAV.
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