The objective of the Tumor Microenvironment and Metastasis Program is to understand the molecular mechanisms involved in the regulation of the survival, differentiation and function of cells in tumors, the microenvironments responsible for invasion and metastasis, and signaling pathways employed. The program is supported by a Program Project grant focused on defining how signaling pathways in macrophages and carcinoma cells contribute to the motility and chemotatic behaviors that generate the invasive phenotype. The major disease site studied is breast but other cancers such as lung are also included. The program has three major goals: (1) Dissection of the role the microenvironment plays in tumor progression and metastasis: There is an emphasis on the interaction between tumor cells and tumor associated macrophages, cells that promote tumor progression and metastasis. These studies utilize, xenotransplants, mouse models, as well as human tumor xenotransplants into immunocompromised mice. Six distinct functions have been identified for macrophages in promoting malignancy. 2) The molecular mechanisms of growth factor and hormone action in regulating cell motility and proliferation. Investigators study the intrinsic mechanisms that feed downstream from receptors in regulating cell motility, chemotaxis, invasion as well as cell proliferation. There is a particular emphasis on signaling from the colony stimulating factor receptor in macrophages and the ErbB family of receptors in tumor cells and the studies utilize a combination of systems, including cell lines in culture and as xenografts, as well as mouse models of breast cancer. 3) Imaging and animal models. This is directed to the development of innovative optical technologies using multiphoton microscopy to image cells and their interactions within the tumor microenvironment in vivo coupled with innovative mouse genetics to label lineages and perturb signaling pathways. There are currently 21 program members from 10 departments, of whom 16 are primary members, supported by 17 NCI ($2.9M Direct) and 10 other NIH grants. There have been 8 new recruits to this program. Since the last CCSG review there have been 246 cancer-relevant research papers by members of this program of which 20% represent intraprogrammatic, and 21% represent interprogrammatic collaborations.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA013330-36
Application #
7680068
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
36
Fiscal Year
2008
Total Cost
$18,057
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
110521739
City
Bronx
State
NY
Country
United States
Zip Code
10461
Zamurrad, Sumaira; Hatch, Hayden A M; Drelon, Coralie et al. (2018) A Drosophila Model of Intellectual Disability Caused by Mutations in the Histone Demethylase KDM5. Cell Rep 22:2359-2369
Sparano, Joseph A (2018) Prognostic gene expression assays in breast cancer: are two better than one? NPJ Breast Cancer 4:11
Centini, Ryan; Tsang, Mark; Iwata, Terri et al. (2018) Loss of Fnip1 alters kidney developmental transcriptional program and synergizes with TSC1 loss to promote mTORC1 activation and renal cyst formation. PLoS One 13:e0197973
Nadaradjane, Celine; Yang, Chia-Ping Huang; Rodriguez-Gabin, Alicia et al. (2018) Improved Dose-Response Relationship of (+)-Discodermolide-Taxol Hybrid Congeners. J Nat Prod 81:607-615
Tiwari, Sangeeta; van Tonder, Andries J; Vilchèze, Catherine et al. (2018) Arginine-deprivation-induced oxidative damage sterilizes Mycobacterium tuberculosis. Proc Natl Acad Sci U S A 115:9779-9784
Celestrin, Kevin; Díaz-Balzac, Carlos A; Tang, Leo T H et al. (2018) Four specific immunoglobulin domains in UNC-52/Perlecan function with NID-1/Nidogen during dendrite morphogenesis in Caenorhabditis elegans. Development 145:
Haider, Afreen; Wei, Yu-Chen; Lim, Koini et al. (2018) PCYT1A Regulates Phosphatidylcholine Homeostasis from the Inner Nuclear Membrane in Response to Membrane Stored Curvature Elastic Stress. Dev Cell 45:481-495.e8
Cai, Ying; Lin, Jhih-Rong; Zhang, Quanwei et al. (2018) Epigenetic alterations to Polycomb targets precede malignant transition in a mouse model of breast cancer. Sci Rep 8:5535
Li, Ke; Baker, Nicholas E (2018) Regulation of the Drosophila ID protein Extra macrochaetae by proneural dimerization partners. Elife 7:
Xie, Xianhong; Xue, Xiaonan; Strickler, Howard D (2018) Generalized linear mixed model for binary outcomes when covariates are subject to measurement errors and detection limits. Stat Med 37:119-136

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