Transgenic Polyoma middle-T mice model premalignant mammary disease

Jeannie E. Maglione, Drew Moghanaki, Lawrence J.T. Young, Cathyryne K. Manner, Lesley G. Ellies, Sasha O. Joseph, Benjamin Nicholson, Robert Cardiff, Carol L. MacLeod

Research output: Contribution to journalArticle

181 Scopus citations

Abstract

Mice transgenic for the Polyomavirus middle T (PyV-mT) gene have been widely used to study mammary tumorigenesis and metastasis. Although numerous molecular insights were gained from the analysis of these transgenic malignant tumors, the early events leading to malignant transformation have not been systematically investigated nor has the biological potential of hyperplastic lesions been documented. This paper presents the first comprehensive histopathological characterization of transgenic PyV-mT hyperplasias together with classical transplantation experiments designed to test the growth potential of these lesions. Moreover, stable hyperplastic outgrowth lines were established as a tool to study premalignant PyV-mT-induced hyperplasias in detail. Each line has a different tumor latency, indicating that PyV-mT-induced hyperplasias, like early proliferative lesions seen in the human breast, are heterogeneous with respect to their malignant potential. Our results settle a controversy; they establish that PyV-mT gene expression alone is insufficient to induce tumors and that additional events are required for tumorigenesis and metastasis. These results support the use of PyV-mT transgenic mice as a model for investigating the multistep progression of malignant mammary tumorigenesis and metastasis.

Original languageEnglish (US)
Pages (from-to)8298-8305
Number of pages8
JournalCancer Research
Volume61
Issue number22
StatePublished - Nov 15 2001

ASJC Scopus subject areas

  • Oncology
  • Cancer Research

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    Maglione, J. E., Moghanaki, D., Young, L. J. T., Manner, C. K., Ellies, L. G., Joseph, S. O., Nicholson, B., Cardiff, R., & MacLeod, C. L. (2001). Transgenic Polyoma middle-T mice model premalignant mammary disease. Cancer Research, 61(22), 8298-8305.