Carcinogenesis, Vol. 20, No. 9, 1747-1753,
September 1999
© 1999 Oxford University Press
Carcinogenesis |
Induction of melanoma in TPras transgenic mice
Arizona Cancer Center, University of Arizona, 1515 North Campbell Avenue, PO Box 245042, Tucson, AZ 85724-5024, USA
In order to study the oncogenesis of melanocytes, transgenic mouse lines were established that express a mutated human Ha-ras (TPras) gene in pigment producing cells. The ras transgenic mice exhibit an altered phenotype, including melanocytic hyperplasia and a muted agouti coat, indicative of hyperproliferative melanocytes. These mice and their wild-type littermates have been subjected to a variety of carcinogenesis protocols, including 7,12-dimethylbenz-[a]anthracene (DMBA), 12-O-tetradecanoylphorbol-13-acetate (TPA) and UV radiation exposure. Topical DMBA treatment of TPras mice resulted in a high incidence of melanomas. Metastatic lesions were observed in skin, lungs and lymph nodes. TPA treatment of TPras mice induced a small number of papillomas but no nevi or melanomas. UV light exposures induced papillomas in negative littermate and melanomas in some albino TPras mice. These results show that melanocytes expressing an activated Ha-ras in the TPras transgenic mice are susceptible to induction of melanoma by DMBA.
Abbreviations: DMBA, 7,12-dimethylbenz[a]anthracene; SCID, severe combined immunodeficient; TPA, 12-O-tetradecanoylphorbol-13-acetate.
1 To whom correspondence should be addressed Email: mbroome{at}azcc.arizona.edu
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