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Publication : Muir-Torre-like syndrome in Fhit-deficient mice.

First Author  Fong LY Year  2000
Journal  Proc Natl Acad Sci U S A Volume  97
Issue  9 Pages  4742-7
PubMed ID  10758156 Mgi Jnum  J:61946
Mgi Id  MGI:1855807 Doi  10.1073/pnas.080063497
Citation  Fong LY, et al. (2000) Muir-torre-like syndrome in fhit-deficient mice. Proc Natl Acad Sci U S A 97(9):4742-7
abstractText  To investigate the role of the Fhit gene in carcinogen induction of neoplasia, we have inactivated one Fhit allele in mouse embryonic stem cells and produced (129/SvJ x C57BL/6J) F(1) mice with a Fhit allele inactivated (+/-). Fhit +/+ and +/- mice were treated intragastrically with nitrosomethylbenzylamine and observed for 10 wk posttreatment. A total of 25% of the +/+ mice developed adenoma or papilloma of the forestomach, whereas 100% of the +/- mice developed multiple tumors that were a mixture of adenomas, squamous papillomas, invasive carcinomas of the forestomach, as well as tumors of sebaceous glands. The visceral and sebaceous tumors, which lacked Fhit protein, were similar to those characteristic of Muir-Torre familial cancer syndrome.
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