? This application in response to the RFA for the Tumor Microenvironment Network (TMEN) will focus on? mouse models of cancer initiation and progression, particularly in the breast and lung and involving both? transplantable and autochthonous (i.e. spontaneous endogenous) tumors. The applicant group is? multidisciplinary, involving investigators expert in mouse models, cancer cell biology, molecular imaging and? proteomics. The individual subprojects will focus on specific components of the tumor microenvironment;? cells, secreted factors and extracellular matrix (collectively termed stroma), as well as on the nature of the? immune response to cancer.? We will investigate the following topics:-? 1. stromal influences on why and how tumor cells initially become invasive and metastatic as a? consequence of stromal effects at the site of the primary tumor.? 2. microenvironmental effects that can suppress or enhance the seeding, survival and growth of metastases? at secondary sites.? 3. the identity and origins of stromal cells (mesenchymal and hematopoietic) induced at, or recruited to, the? site of a primary tumor, how they are recruited, and how they affect the progression of the tumor? 4. the nature of immune surveillance of autochthonous tumors? 5. the nature of different tumor extracellular matrices (ECMs) and interactions of both tumor and stromal? cells with ECM? 6. we will further develop novel imaging probes and methods to detect, track and ablate different subsets of? stromal cells in mouse models of cancer.? 7. we will use lentiviral-mediated RNA interference both to initiate autochthonous tumors and to manipulate? the functions of both tumor and stromal cells.? It is becoming increasingly recognized that tumor cells do not progress to malignancy in isolation - the? microenvirnment of the tumor can either enhance or suppress tumor growth and progression. This program? will provide new information and novel technological approaches to questions concerning the effects of the? surrounding microenvironment in which tumors develop. It is expected that new insights from this research? will offer novel approaches to intervene in the progression of tumors to malignancy.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Specialized Center--Cooperative Agreements (U54)
Project #
5U54CA126515-03
Application #
7491219
Study Section
Special Emphasis Panel (ZCA1-SRRB-3 (O1))
Program Officer
Mohla, Suresh
Project Start
2006-09-30
Project End
2011-08-31
Budget Start
2008-09-01
Budget End
2009-08-31
Support Year
3
Fiscal Year
2008
Total Cost
$1,145,130
Indirect Cost
Name
Massachusetts Institute of Technology
Department
Internal Medicine/Medicine
Type
Schools of Arts and Sciences
DUNS #
001425594
City
Cambridge
State
MA
Country
United States
Zip Code
02139
Naba, Alexandra; Pearce, Oliver M T; Del Rosario, Amanda et al. (2017) Characterization of the Extracellular Matrix of Normal and Diseased Tissues Using Proteomics. J Proteome Res 16:3083-3091
Ragelle, Héloïse; Naba, Alexandra; Larson, Benjamin L et al. (2017) Comprehensive proteomic characterization of stem cell-derived extracellular matrices. Biomaterials 128:147-159
Gocheva, Vasilena; Naba, Alexandra; Bhutkar, Arjun et al. (2017) Quantitative proteomics identify Tenascin-C as a promoter of lung cancer progression and contributor to a signature prognostic of patient survival. Proc Natl Acad Sci U S A 114:E5625-E5634
Engblom, Camilla; Pfirschke, Christina; Zilionis, Rapolas et al. (2017) Osteoblasts remotely supply lung tumors with cancer-promoting SiglecFhigh neutrophils. Science 358:
Naba, Alexandra; Clauser, Karl R; Mani, D R et al. (2017) Quantitative proteomic profiling of the extracellular matrix of pancreatic islets during the angiogenic switch and insulinoma progression. Sci Rep 7:40495
Pucci, Ferdinando; Garris, Christopher; Lai, Charles P et al. (2016) SCS macrophages suppress melanoma by restricting tumor-derived vesicle-B cell interactions. Science 352:242-6
Pfirschke, Christina; Engblom, Camilla; Rickelt, Steffen et al. (2016) Immunogenic Chemotherapy Sensitizes Tumors to Checkpoint Blockade Therapy. Immunity 44:343-54
Naba, Alexandra; Clauser, Karl R; Ding, Huiming et al. (2016) The extracellular matrix: Tools and insights for the ""omics"" era. Matrix Biol 49:10-24
Pucci, Ferdinando; Rickelt, Steffen; Newton, Andita P et al. (2016) PF4 Promotes Platelet Production and Lung Cancer Growth. Cell Rep 17:1764-1772
Naba, Alexandra; Clauser, Karl R; Hynes, Richard O (2015) Enrichment of Extracellular Matrix Proteins from Tissues and Digestion into Peptides for Mass Spectrometry Analysis. J Vis Exp :e53057

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