Salmonella-mediated tumor-targeting TRAIL gene therapy significantly suppresses melanoma growth in mouse model

被引:57
作者
Chen, Jianxiang [1 ,2 ]
Yang, Bingya [1 ,2 ]
Cheng, Xiawei [1 ,2 ]
Qiao, Yiting [1 ,2 ]
Tang, Bo [1 ,2 ,3 ,4 ]
Chen, Guo [1 ,2 ]
Wei, Jing [1 ,2 ]
Liu, Xiufeng [1 ,2 ]
Cheng, Wei [1 ,2 ]
Du, Pan [1 ,2 ]
Huang, Xiaofeng [1 ,2 ]
Jiang, Wenhui [1 ,2 ]
Hu, Qingang [1 ,2 ]
Hu, Yiqiao [1 ,2 ]
Li, Jiahuang [1 ,2 ]
Hua, Zi-Chun [1 ,2 ,3 ,4 ]
机构
[1] Nanjing Univ, Affiliated Stomatol Hosp, State Key Lab Pharmaceut Biotechnol, Nanjing, Jiangsu, Peoples R China
[2] Nanjing Univ, Affiliated Stomatol Hosp, Sch Stomatol, Nanjing, Jiangsu, Peoples R China
[3] Nanjing Univ, Changzhou High Tech Res Inst, Changzhou, Peoples R China
[4] Jiangsu TargetPharma Labs, Changzhou, Peoples R China
关键词
ATTENUATED SALMONELLA; STREPTOCOCCUS-MUTANS; SOLID TUMORS; EXPRESSION; CANCER; HYPOXIA; TYPHIMURIUM; DELIVERY; PROMOTER; VNP20009;
D O I
10.1111/j.1349-7006.2011.02147.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Attenuated Salmonella typhimurium (S. typhimurium) strains can selectively grow and express exogenous genes in tumors for targeted therapy. We engineered S. typhimurium strain VNP20009 to secrete tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) under the control of a hypoxia-induced nirB promoter and examined the efficacy of Salmonella-mediated targeted expression of TRAIL in mice bearing melanoma tumor and in TRAIL-resistant RM-1 tumor. We found that VNP preferentially accumulated in tumor tissues and the nirB promoter effectively drove targeted expression of TRAIL. Compared with recombinant TRAIL protein and VNP20009 combination therapy, VNP20009 expressing TRAIL significantly suppressed melanoma growth but failed to suppress RM-1 tumor growth. Furthermore, we confirmed that VNP20009 expressing TRAIL yielded its antitumor effect by inducing melanoma apoptosis. Our findings indicate that Salmonella-mediated tumor-targeted therapy with TRAIL could reduce tumor growth and extend host survival. (Cancer Sci 2012; 103: 325333)
引用
收藏
页码:325 / 333
页数:9
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