Visualization of tumors and metastases in live animals with bacteria and vaccinia virus encoding light-emitting proteins

被引:336
作者
Yu, YA
Shabahang, S
Timiryasova, TM
Zhang, Q
Beltz, R
Gentschev, I
Goebel, R
Szalay, AA [1 ]
机构
[1] Loma Linda Univ, Sch Med, Dept Biochem, Loma Linda, CA 92350 USA
[2] Loma Linda Univ, Sch Med, Ctr Mol Biol & Gene Therapy, Loma Linda, CA 92350 USA
[3] Genelux Corp, San Diego Sci Ctr, San Diego, CA 92109 USA
[4] Univ Wurzburg, Bioctr, Dept Microbiol, D-97074 Wurzburg, Germany
[5] Univ Wurzburg, DFG Res Ctr Expt Biomed, Rudolf Virchow Ctr, D-97074 Wurzburg, Germany
关键词
D O I
10.1038/nbt937
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
We have shown that bacteria injected intravenously into live animals entered and replicated in solid tumors and metastases. The tumor-specific amplification process was visualized in real time using luciferase-catalyzed luminescence and green fluorescent protein fluorescence, which revealed the locations of the tumors and metastases. Escherichia coli and three attenuated pathogens (Vibrio cholerae, Salmonella typhimurium, and Listeria monocytogenes) all entered tumors and replicated. Similarly, the cytosolic vaccinia virus also showed tumor-specific replication, as visualized by real-time imaging. These findings indicate that neither auxotrophic mutations, nor vaccinia virus deficient for the thymidine kinase gene, nor anaerobic growth conditions were required for tumor specificity and intratumoral replication. We observed localization of tumors by light-emitting microorganisms in immunocompetent and in immunocompromised rodents with syngeneic and allogeneic tumors. Based on their 'tumor-finding' nature, bacteria and viruses may be designed to carry multiple genes for detection and treatment of cancer.
引用
收藏
页码:313 / 320
页数:8
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