Expression of Escherichia coli B nitroreductase in established human tumor xenografts in mice results in potent antitumoral and bystander effects upon systemic administration of the prodrug CB1954

被引:53
作者
Djeha, AH
Hulme, A
Dexter, MT
Mountain, A
Young, LS
Searle, PF
Kerr, DJ
Wrighton, CJ
机构
[1] Univ Keele, Cobra Therapeut Ltd, Keele ST5 5BG, Staffs, England
[2] Paterson Inst Canc Res, Sect Haemopoiet Cell & Gene Therapeut, Canc Res Campaign, Manchester M20 9BX, Lancs, England
[3] Univ Birmingham, Inst Canc Studies, Canc Res Campaign, Birmingham, W Midlands, England
关键词
gene-directed enzyme prodrug therapy; nitroreductase; CB1954; hepatocellular carcinoma; squamous carcinoma; naked DNA;
D O I
10.1038/sj.cgt.7700171
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Expression of the Escherichia coli enzyme nitroreductase (NTR) in mammalian cells enables them to activate the prodrug 5-(afiridin-1-yl)-2,4-dinitrobenzamide (CB1954), leading to interstrand DNA cross-linking and apoptosis in both proliferating and quiescent cells. In the work reported here, we used human hepatocellular carcinoma and squamous carcinoma cell lines constitutively expressing NTR to demonstrate that the ntr/CB1954 system results in potent, long-lasting antitumoral effects in mice. We also demonstrate that this enzyme/prodrug combination results in antitumoral effects in vivo when only a minority of tumor cells express the enzyme, using either cells constitutively expressing NTR or ntr gene delivery in situ.
引用
收藏
页码:721 / 731
页数:11
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