Abstract
To overcome difficulties that hampered widespread application of a specific delivery system in cancer gene therapy and to inhibit the growth of solid liver cancer, we utilized a strain of Bifidobacterium longum as a delivery system to transport an endostatin gene that can inhibit growth of tumor. The B. longum strain with the endostatin gene (B. longum-En) was taken orally by tumor-bearing nude mice through drencher preparation. The results showed that B. longum-En could strongly inhibit the growth of solid liver tumor in nude mice and prolong the survival time of tumor-bearing nude mice. Furthermore, tumor growth was inhibited more efficiently when the B. longum-En treatment included selenium. Enriching the B. longum-En treatment with selenium improves the activity of NK and T cells and stimulates the activity of IL-2 and TNF-α in BALB/c mice. These results suggest that B. longum may be a highly specific and efficient vector for transporting anticancer genes in cancer gene therapy.
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Acknowledgements
We thank Dr Amy Lawton-Rauh and Dr Bao-Hua Song (Department of Genetics and Evolution, Max Planck Institute of Chemical Ecology, Beutenberg Campus) for reading this manuscript.
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Fu, GF., Li, X., Hou, YY. et al. Bifidobacterium longum as an oral delivery system of endostatin for gene therapy on solid liver cancer. Cancer Gene Ther 12, 133–140 (2005). https://doi.org/10.1038/sj.cgt.7700758
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DOI: https://doi.org/10.1038/sj.cgt.7700758
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