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Seeding and propagation of untransformed mouse mammary cells in the lung.

ABSTRACT: The acquisition of metastatic ability by tumor cells is considered a late event in the evolution of malignant tumors. We report that untransformed mouse mammary cells that have been engineered to express the inducible oncogenic transgenes MYC and Kras(D12), or polyoma middle T, and introduced into the systemic circulation of a mouse can bypass transformation at the primary site and develop into metastatic pulmonary lesions upon immediate or delayed oncogene induction. Therefore, previously untransformed mammary cells may establish residence in the lung once they have entered the bloodstream and may assume malignant growth upon oncogene activation. Mammary cells lacking oncogenic transgenes displayed a similar capacity for long-term residence in the lungs but did not form ectopic tumors.

SUBMITTER: Podsypanina K

PROVIDER: S-EPMC2694414 | biostudies-literature | 2008 Sep

REPOSITORIES: biostudies-literature

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Seeding and propagation of untransformed mouse mammary cells in the lung.

Podsypanina Katrina K Du Yi-Chieh Nancy YC Jechlinger Martin M Beverly Levi J LJ Hambardzumyan Dolores D Varmus Harold H

Science (New York, N.Y.) 20080828 5897

The acquisition of metastatic ability by tumor cells is considered a late event in the evolution of malignant tumors. We report that untransformed mouse mammary cells that have been engineered to express the inducible oncogenic transgenes MYC and Kras(D12), or polyoma middle T, and introduced into the systemic circulation of a mouse can bypass transformation at the primary site and develop into metastatic pulmonary lesions upon immediate or delayed oncogene induction. Therefore, previously untra ...[more]

PMID: 18755941

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