Exogeneous cytosine deaminase gene expression in Bifidobacterium breve 1-53-8w for tumor-targeting enzyme/prodrug therapy

被引:28
作者
Hidaka, Ayurni [1 ]
Hamaji, Yoshinori [1 ]
Sasaki, Takayuki [1 ]
Taniguchi, Shun'ichiro [2 ]
Fujimori, Minoru [1 ]
机构
[1] Shinshu Univ, Sch Med, Dept Surg, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Grad Sch Med, Inst Aging & Adaptat, Dept Mol Oncol, Matsumoto, Nagano 3908621, Japan
基金
日本学术振兴会;
关键词
Bifidobacterium breve; plasmid; cytosine deaminase; enzyme/prodrug therapy; 5-fluorouracil (5-FU);
D O I
10.1271/bbb.70284
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Bifidobacteria are nonpathogenic, anaerobic domestic bacteria with health-promoting properties for the host. In our previous study, Bifidobacterium longum (B. longum) were found to be localized selectively and to proliferate within solid tumors after systemic application. Additionally, B. longum transformed by shuttle-plasmid including the cytosine deaminase (CD) gene expressed active CD, converted the prodrug 5-fluorocytosine (5-FC) to 5-fluorouracil (5-FU). We also demonstrated antitumor efficacy with a transformant of B. longum in rats. In this study, we found that Bifidobacterium breve (B. breve), the smallest species of human-derived bifidobacterium, expressed the exogenous transgene (CD), that CD enzymatic activity in the transformant of B. breve was much higher, and that the segregational stability of the plasmid was greater than that of B. longum. Thus, numerous transformants of B. breve were detected solely in the tumors after systemic administration. We consider the transformant of B. breve to be. more beneficial in our enzyme/prodrug therapy.
引用
收藏
页码:2921 / 2926
页数:6
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