The PPG has as its central aim the understanding of cell motility and invasion with its focus upon cellularinteractions in the tumor microenvironment. These interactions can only be effectively modeled in mice andCore C provides access to mouse models of breast cancer. It allows the rapid testing (in the context ofmouse breeding and genetic manipulation) of hypotheses about the importance of particular signalingmolecules in the process of tumor invasion and metastasis.. The core generates genetically manipulatedmice and provides access to techniques used by many investigators including, staging of mammary tumors,mammary fat pad transplantation, lung metastasis assays and intravenous injections. The PPG haspioneered the intravital imaging of different cell types within the tumor. This requires individual lineages tobe marked with fluorescent proteins expressed from lineage specific promoters. To date both macrophages,endothelial and tumor cells are labeled with GFP or CFP and each of these strains are crossed withmammary tumor bearing mice. Core C maintains all these colonies and performs the multiple crosses,providing genotyping and colony maintenance services. Such large-scale mouse breeding would beimpossible for any one laboratory. Furthermore, without this core, many of the members of the projectprogram who are cell biologists and biochemists, would find it very difficult to translate their fundamentalobservations in cultured cells into testable hypotheses about their role in tumor progression in vivo.
The specific aims are:1) Develop and maintain mice in which multiple cell lineages are marked by expression of fluorescentproteins. These are carried on both the MMTV-Polyoma and Her2/Neu mammary tumor-bearing mice.2) Genetically manipulate the mouse genome in ways relevant to the PPG and develop methodology toconditionally ablate specific genes in individual cell lineages.3) Provide assistance in tumor staging and metastasis assays.4) Provide other techniques relevant to the PPG such as bone marrow transplantation; mammarytransplantation, transgenic and gene targeting construct advice.Breast cancer is the most common cancer of women in Europe and the US causing great morbidity andmortality. Our studies have indicated an important role for the tumor microenvironment modulatingmetastasis. This complex interaction between cells can only be modeled in mice. Insight gained form thesestudies should help in the development of therapeutics that inhibit metastasis.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
2P01CA100324-06
Application #
7534112
Study Section
Special Emphasis Panel (ZCA1-RPRB-O (M1))
Project Start
2008-06-01
Project End
2013-05-31
Budget Start
2008-09-15
Budget End
2009-05-31
Support Year
6
Fiscal Year
2008
Total Cost
$304,044
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
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