The role of the microenvironment in tumor progression is an emerging area of research that clearly has important clinical implications, both for diagnosis and treatment of human carcinoma. The conversion of normal epithelial cells to metastatic tumor cells is accepted as a multi-stage process that requires progressive genetic alterations within the epithelial tumor cell and has been the focus of intense investigation. However, the many other cell types in the tumor microenvironment are increasingly appreciated as components of a complex biological network, akin to an organ system, that are critical for tumor progression. The members of this Program Project Grant will use both human genetic approaches and mouse genetic models to study gene action from two cell types in the tumor microenvironment: tumor stromal fibroblasts and macrophages. The program consists of three interactive Projects supported by four Cores. Project 1 will use human genetic approaches and laser capture microdissection to analyze genetic alterations that occur in the stromal compartment of human breast cancer samples. Projects 1, 2 and 3 will develop and use mouse models to experimentally test the role of three genetic pathways: Pten, Rb/E2F and ras/ets-2 in the tumor microenvironment. This work will be supported by the Transgenic/Knockout Core, the Mouse Pathology Core, the Research Methods and Biostatistics Core and the Administrative Core. The major, immediate goals of this program are: 1) identification on a genome-wide scale of genetic alterations that occur in mammary tumor stromal cells isolated from human mammary tumor samples and the correlation of genetic changes found in mammary tumor stroma with clinical outcome of breast cancer patients; 2) experimental verification of the essential role of gene action from mammary stromal cells during mammary tumor progression. This involves creation of mouse models that allow gene action in cells of the microenvironment to be tested and that should more accurately reflect mammary tumor progression in humans at the genetic level. The long-term goal of this Program is to use the information gained from our increased understanding of the role of the tumor microenvironment in breast cancer progress to improve strategies for the diagnosis, prognostication and treatment of human breast cancer.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA097189-05
Application #
7484275
Study Section
Subcommittee G - Education (NCI)
Program Officer
Snyderwine, Elizabeth G
Project Start
2004-09-15
Project End
2011-07-31
Budget Start
2008-08-01
Budget End
2011-07-31
Support Year
5
Fiscal Year
2008
Total Cost
$1,677,075
Indirect Cost
Name
Ohio State University
Department
Biochemistry
Type
Schools of Medicine
DUNS #
832127323
City
Columbus
State
OH
Country
United States
Zip Code
43210
Sizemore, Steven T; Mohammad, Rahman; Sizemore, Gina M et al. (2018) Synthetic Lethality of PARP Inhibition and Ionizing Radiation is p53-dependent. Mol Cancer Res 16:1092-1102
Pitarresi, Jason R; Liu, Xin; Avendano, Alex et al. (2018) Disruption of stromal hedgehog signaling initiates RNF5-mediated proteasomal degradation of PTEN and accelerates pancreatic tumor growth. Life Sci Alliance 1:e201800190
Ahirwar, Dinesh K; Nasser, Mohd W; Ouseph, Madhu M et al. (2018) Fibroblast-derived CXCL12 promotes breast cancer metastasis by facilitating tumor cell intravasation. Oncogene 37:4428-4442
Rudolph, M; Sizemore, S T; Lu, Y et al. (2018) A hedgehog pathway-dependent gene signature is associated with poor clinical outcomes in Luminal A breast cancer. Breast Cancer Res Treat 169:457-467
Sizemore, Gina M; Balakrishnan, Subhasree; Thies, Katie A et al. (2018) Stromal PTEN determines mammary epithelial response to radiotherapy. Nat Commun 9:2783
Victor, Aaron R; Nalin, Ansel P; Dong, Wenjuan et al. (2017) IL-18 Drives ILC3 Proliferation and Promotes IL-22 Production via NF-?B. J Immunol 199:2333-2342
Liu, Huayang; Dowdle, James A; Khurshid, Safiya et al. (2017) Discovery of Stromal Regulatory Networks that Suppress Ras-Sensitized Epithelial Cell Proliferation. Dev Cell 41:392-407.e6
Tang, Xing; Srivastava, Arunima; Liu, Huayang et al. (2017) annoPeak: a web application to annotate and visualize peaks from ChIP-seq/ChIP-exo-seq. Bioinformatics 33:1570-1571
Sizemore, G M; Balakrishnan, S; Hammer, A M et al. (2017) Stromal PTEN inhibits the expansion of mammary epithelial stem cells through Jagged-1. Oncogene 36:2297-2308
Hammer, Anisha M; Sizemore, Gina M; Shukla, Vasudha C et al. (2017) Stromal PDGFR-? Activation Enhances Matrix Stiffness, Impedes Mammary Ductal Development, and Accelerates Tumor Growth. Neoplasia 19:496-508

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