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PMID: 9679770 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Identification of inbred mouse strains harboring genetic modifiers of mammary tumor age of onset and metastatic progression.

International journal of cancer ·Vol. 77 ·No. 4 ·1998-08-12 ·Pages 640-4

Lifsted T, Le Voyer T, Williams M, Muller W, Klein-Szanto A, Buetow KH, Hunter KW

Abstract

Metastasis is one of the most important and complex processes in human neoplastic disease. A large number of both positive and negative events must occur to permit a tumor cell to colonize a distant site successfully. To identify mouse strains that harbor dominant genetic modifiers of this process, a strain survey was initiated utilizing a transgenic mouse mammary tumor model that exhibits a high incidence of pulmonary metastases. The transgenic animal was bred to 27 different inbred strains of mice and scored for the metastatic organ tropism and metastatic density. Thirteen strains were identified that had a statistically significant reduction in the numbers of pulmonary metastases. In addition, 10 strains were identified that altered the kinetics of induction of the primary mammary tumor. These strains will likely provide useful model systems for the analysis of genetic interactions in the initiation and progression of mammary adenocarcinomas.

MeSH Terms
Age of Onset Animals Disease Progression Female Genes, Dominant Lung Neoplasms/secondary Male Mammary Neoplasms, Animal/genetics,secondary Mice Mice, Inbred Strains/genetics Mice, Transgenic/genetics Transgenes
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Lifsted T
Division of Population Science, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Le Voyer T
Williams M
Muller W
Klein-Szanto A
Buetow K H
Hunter K W
Article Info
Journal
International journal of cancer
Abbr.
Int J Cancer
ISSN
0020-7136
Published
1998-08-12
Pages
640-4
Language
English
Region
United States
NLM ID
0042124
Subset
IM
Grants
NCI NIH HHS · CA06927 · United States
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