Core C is the animal core and provides essential services to all projects in the PPG. It provides access for PPG members to complex mouse genetic models of breast cancer and allows genetic investigation into the mechanisms of tumor progression and metastasis. The core has pioneered the lineage labeling of particular cell types and'has been essential to many of the major findings of the PPG, especially those involving macrophage-tumor cell interactions. In the next granting period, models of breast cancer will be maintained with lineage marked cells in order to study complex behaviors after genetic manipulation in vivo. The core has also developed lineages marked with photo-switchable fluorescent proteins that will be essential to fate mapping of macrophages and tumor cells in the next funding period. The Core has also developed novel macrophage restricted cre recombinases both constitutive and inducible, as well as new more efficient and restricted mammary epithelial specific cres. The core will also develop new methodologies with novel fluorescent proteins and lineage tracing methods during the next granting period.

Public Health Relevance

Breast cancer is one of the most common cancers of women in the US causing great morbidity and mortality. The studies in the PPG have indicated an important role for the tumor microenvironment and in particular macrophages in modulating metastasis. This complex interaction between cells can only be modeled in mice and the core provides access to all members of the PPG to test their hypotheses in complex genetic models. Insight gained form these studies should help in the development of therapeutics that inhibit metastasis.

National Institute of Health (NIH)
National Cancer Institute (NCI)
Research Program Projects (P01)
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Special Emphasis Panel (ZCA1-RPRB-C (J1))
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Albert Einstein College of Medicine
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Al-Dimassi, Saleh; Salloum, Gilbert; Saykali, Bechara et al. (2016) Targeting the MAP kinase pathway in astrocytoma cells using a recombinant anthrax lethal toxin as a way to inhibit cell motility and invasion. Int J Oncol 48:1913-20
Balsamo, Michele; Mondal, Chandrani; Carmona, Guillaume et al. (2016) The alternatively-included 11a sequence modifies the effects of Mena on actin cytoskeletal organization and cell behavior. Sci Rep 6:35298
Chitu, Violeta; Gokhan, Şölen; Nandi, Sayan et al. (2016) Emerging Roles for CSF-1 Receptor and its Ligands in the Nervous System. Trends Neurosci 39:378-93
Leung, E; Xue, A; Wang, Y et al. (2016) Blood vessel endothelium-directed tumor cell streaming in breast tumors requires the HGF/C-Met signaling pathway. Oncogene :
Knutsdottir, Hildur; Condeelis, John S; Palsson, Eirikur (2016) 3-D individual cell based computational modeling of tumor cell-macrophage paracrine signaling mediated by EGF and CSF-1 gradients. Integr Biol (Camb) 8:104-19
Pignatelli, Jeanine; Bravo-Cordero, Jose Javier; Roh-Johnson, Minna et al. (2016) Macrophage-dependent tumor cell transendothelial migration is mediated by Notch1/Mena(INV)-initiated invadopodium formation. Sci Rep 6:37874
Wang, Yarong; Wang, Haoxuan; Li, Jiufeng et al. (2016) Direct visualization of the phenotype of hypoxic tumor cells at single cell resolution in vivo using a new hypoxia probe. Intravital 5:
Pollard, Jeffrey W (2016) Defining Metastatic Cell Latency. N Engl J Med 375:280-2
Rodriguez-Tirado, Carolina; Kitamura, Takanori; Kato, Yu et al. (2016) Long-term High-Resolution Intravital Microscopy in the Lung with a Vacuum Stabilized Imaging Window. J Vis Exp :
Lewis, Claire E; Harney, Allison S; Pollard, Jeffrey W (2016) The Multifaceted Role of Perivascular Macrophages in Tumors. Cancer Cell 30:18-25

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