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Toxicologic Pathology, Vol. 29, No. 1 suppl, 81-89 (2001)
DOI: 10.1080/019262301753178492

The rasH2 Transgenic Mouse: Nature of the Model and Mechanistic Studies on Tumorigenesis

Norikazu Tamaoki

Tokai University School of Medicine, Central Institute for Experimental Animals, 1430 Nogawa, Miyamae, Kawasaki, 216-0001, Japan

The rasH2 mouse is a hemizygous transgenic mouse carrying the c-Ha-ras oncogene and that gene's promotor/enhancer within the genetic background of a BALB/cByJ C57BL/6J F1 mouse. Approximately 3 copies of the transgene are integrated in a tandem array into chromosome number 15. The transgene is transmitted stably without point mutation in hot spots and is expressed in all tissues over 20 backcross generations. The homozygous c-Ha-ras genotype is lethal. Hemizygotes are selected by polymerase chain reaction (PCR) analysis of tail tips after birth. Spontaneous tumors in hemizygous transgenic mice are rare until 6 months of age. The observed rasH2 tumor spectrum, including lung adenoma/adenocarcinoma, forestomach and skin papillomas, Harderian gland adenoma, liver proliferative lesions, splenic hemangioma/sarcoma, and lymphoma is consistent with the BALB/c and C57BL/6 background. In the rasH2 mouse, point mutations of the transgene induced by genotoxins are reported frequently but not in all tumors. Elevated levels of transgene expression were detected in all genotoxin-induced tumors in the rasH2. Increased transgene expression was independent of the mutation rate in transgenic and endogenous ras genes. These observations suggest that the overexpression of transgenic c-Ha-ras is responsible for accelerated tumor development.

Key Words: Carcinogenesis • carcinogenicity testing • c-Ha-ras • oncogene expression • oncogene mutation • ras oncogene • transgenic mouse.


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