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Publication : FHIT gene therapy prevents tumor development in Fhit-deficient mice.

First Author  Dumon KR Year  2001
Journal  Proc Natl Acad Sci U S A Volume  98
Issue  6 Pages  3346-51
PubMed ID  11248081 Mgi Jnum  J:68073
Mgi Id  MGI:1932009 Doi  10.1073/pnas.061020098
Citation  Dumon KR, et al. (2001) FHIT gene therapy prevents tumor development in Fhit-deficient mice. Proc Natl Acad Sci U S A 98(6):3346-51
abstractText  The tumor suppressor gene FHIT spans a common fragile site and is highly susceptible to environmental carcinogens. FHIT inactivation and loss of expression is found in a large fraction of premaligant and malignant lesions. In this study, we were able to inhibit tumor development by oral gene transfer, using adenoviral or adenoassociated viral vectors expressing the human FHIT gene, in heterozygous Fhit(+/-) knockout mice, that are prone to tumor development after carcinogen exposure. We therefore suggest that FHIT gene therapy could be a novel clinical approach not only in treatment of early stages of cancer, but also in prevention of human cancer.
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