- TUMOR MICROENVIRONMENT AND METASTASIS PROGRAM Research in the Tumor Microenvironment and Metastasis (TMM) program is directed to defining the mechanisms by which the microenvironment initiates and sustains systemic dissemination of cancers based on interactions between tumor and stromal cells. Program goals include (i) identification of stromal cell types responsible for migratory and disseminating tumor cell phenotypes, (ii) development of in vitro models and cell lines to elucidate the mechanisms for stromal cell induction of tumor cell dissemination, and the discovery of prognostic markers based on these mechanisms, (iii) characterization of molecular mechanisms of growth factor and cytokine actions that regulate cell migration, dissemination, angiogenesis and invasion of distant sites by tumor cells through elucidating intrinsic regulatory, downstream mechanisms, (iv) elucidation of the role of surface molecules and their associated cytoskeletal proteins in tumor cell behavior and metastatic phenotype. A variety of systems are utilized, including cell lines in vitro, animal models in vivo and xenografts, transgenic mouse models of breast cancer and unique biophysical and cell biology tools. A unique aspect of this program is the development of innovative imaging technologies for the study of tumor microenvironment- driven metastasis in vivo that allows documentation of the longitudinal progression of cancers in all sites and stages. These studies encompass: (i) development of large-volume, high-resolution multiphoton intravital imaging to directly observe the initiation of tumors and their dissemination in order to elucidate the underlying mechanisms, (ii) the development of permanent imaging windows for primary and secondary sites for documentation of single cell phenotype, fate and contribution to metastasis, and (iii) the development of novel tumor indwelling microfluidic devices that deliver precise signals to the tumor microenvironment. The over- arching goal of this program, and a major focus since 2013, is the translation of basic mechanistic findings in the laboratory to mouse models with translation to correlative, preventive and therapeutic initiatives in the clinic. Ongoing clinical studies are focused on developing independent, novel correlates of risk of breast cancer progression and metastasis, along with pharmacological interventions in patients conducted by members of the Experimental Therapeutics program. Likewise, there are ongoing studies to translate MRI-based imaging technology from mouse models into imaging protocols in patients that will allow noninvasive in vivo assessment of metastatic risk and response to treatment. While a major focus of research has been on breast cancer, the TMM program now includes research in head and neck, thyroid, pancreatic and other cancers. There are 20 program members from 9 departments. Current NCI funding is 2.3M (dc); total peer-reviewed funding is 4.7M (dc). There have been 297 publications since July 2013 of which 23% represent intra- programmatic, 26% inter-programmatic, and 58% represent collaborations with investigators at other institutions.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA013330-48
Application #
9998885
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
1997-06-01
Project End
2022-06-30
Budget Start
2020-07-01
Budget End
2021-06-30
Support Year
48
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Type
DUNS #
081266487
City
Bronx
State
NY
Country
United States
Zip Code
10461
Mocholi, Enric; Dowling, Samuel D; Botbol, Yair et al. (2018) Autophagy Is a Tolerance-Avoidance Mechanism that Modulates TCR-Mediated Signaling and Cell Metabolism to Prevent Induction of T Cell Anergy. Cell Rep 24:1136-1150
Mao, Serena P H; Park, Minji; Cabrera, Ramon M et al. (2018) Loss of amphiregulin reduces myoepithelial cell coverage of mammary ducts and alters breast tumor growth. Breast Cancer Res 20:131
Guan, Fangxia; Tabrizian, Tahmineh; Novaj, Ardijana et al. (2018) Dietary Walnuts Protect Against Obesity-Driven Intestinal Stem Cell Decline and Tumorigenesis. Front Nutr 5:37
Yang, Chia-Ping Huang; Wang, Changwei; Ojima, Iwao et al. (2018) Taxol Analogues Exhibit Differential Effects on Photoaffinity Labeling of ?-Tubulin and the Multidrug Resistance Associated P-Glycoprotein. J Nat Prod 81:600-606
Chennamadhavuni, Divya; Saavedra-Avila, Noemi Alejandra; Carreño, Leandro J et al. (2018) Dual Modifications of ?-Galactosylceramide Synergize to Promote Activation of Human Invariant Natural Killer T Cells and Stimulate Anti-tumor Immunity. Cell Chem Biol 25:571-584.e8
Wang, Tao; Hosgood, H Dean; Lan, Qing et al. (2018) The Relationship Between Population Attributable Fraction and Heritability in Genetic Studies. Front Genet 9:352
Rocha, Agostinho G; Franco, Antonietta; Krezel, Andrzej M et al. (2018) MFN2 agonists reverse mitochondrial defects in preclinical models of Charcot-Marie-Tooth disease type 2A. Science 360:336-341
Limi, Saima; Senecal, Adrien; Coleman, Robert et al. (2018) Transcriptional burst fraction and size dynamics during lens fiber cell differentiation and detailed insights into the denucleation process. J Biol Chem 293:13176-13190
Cabahug-Zuckerman, Pamela; Stout Jr, Randy F; Majeska, Robert J et al. (2018) Potential role for a specialized ?3 integrin-based structure on osteocyte processes in bone mechanosensation. J Orthop Res 36:642-652
Vilchèze, Catherine; Copeland, Jacqueline; Keiser, Tracy L et al. (2018) Rational Design of Biosafety Level 2-Approved, Multidrug-Resistant Strains of Mycobacterium tuberculosis through Nutrient Auxotrophy. MBio 9:

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