The primary goals of the Solid Tumors Program are to develop novel molecularly-targeted approaches for prevention and treatment of malignancies arising from mucocutaneous, urogenital, and gut epithelia and mesenchymal tissues and to design and conduct translational clinical trials based on findings in basic and/or population research studies. There are 27 full and 9 associate members in this program. Members have 126 active funded projects, which provide over $22 million in funding. Of these, 27 NCI grants account for $3.3 million. Program 3 researchers apply cellular, molecular biological, and genetic techniques to advance understanding of molecular pathogenesis. This new program evolved by integrating two original programs, the well-established Hormonal and Reproductive Cancers and The Gastrointestinal Malignancies Programs. The newly organized program incorporates research work reviewed favorably in the previous competing renewal into a research network optimally supportive for translational research, an area of previous concern. Research in this new program involves studies of normal and malignant cells, as well as inherited diseases that predispose to the development of epithelial malignancies by combined mechanisms of genetic instability and microenvironmental perturbations. Translational studies along with Program 2, Hematologic, have led us to discover, develop, and deliver new treatments for solid tumors, highlighted by molecular therapy of GISTs. Our members have defined new standards of care for total colonic surveillance in colorectal cancer, determined the role of stem cell transplant in poor-risk germ cell cancer, and improved prostate cancer therapy using high-dose calcitriol. We also have developed new murine conditional-knockout models of epithelial carcinogenesis, discovered Herstatin (an inhibitor of EGF and Her2/neu signal transduction) and are clarifying an essential role of IGF signaling and Fanconi pathway dysfunction in clonal progression of epithelial malignancies of the prostate and ovary. The program provides a successful framework that promotes interactions between basic scientists involved in research on epithelial cell survival, differentiation, and clonal evolution and clinicians treating these disorders who also develop translational clinical trials.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA069533-10
Application #
7311035
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2006-06-01
Budget End
2007-05-31
Support Year
10
Fiscal Year
2006
Total Cost
$15,829
Indirect Cost
Name
Oregon Health and Science University
Department
Type
DUNS #
096997515
City
Portland
State
OR
Country
United States
Zip Code
97239
Krey, Jocelyn F; Scheffer, Deborah I; Choi, Dongseok et al. (2018) Mass spectrometry quantitation of proteins from small pools of developing auditory and vestibular cells. Sci Data 5:180128
Rozanov, Dmitri V; Rozanov, Nikita D; Chiotti, Kami E et al. (2018) MHC class I loaded ligands from breast cancer cell lines: A potential HLA-I-typed antigen collection. J Proteomics 176:13-23
Winters-Stone, Kerri M; Wood, Lisa J; Stoyles, Sydnee et al. (2018) The Effects of Resistance Exercise on Biomarkers of Breast Cancer Prognosis: A Pooled Analysis of Three Randomized Trials. Cancer Epidemiol Biomarkers Prev 27:146-153
Pennock, Nathan D; Martinson, Holly A; Guo, Qiuchen et al. (2018) Ibuprofen supports macrophage differentiation, T cell recruitment, and tumor suppression in a model of postpartum breast cancer. J Immunother Cancer 6:98
Xu, Li; Gordon, Ryan; Farmer, Rebecca et al. (2018) Precision therapeutic targeting of human cancer cell motility. Nat Commun 9:2454
Chen, Emerson Y; Blanke, Charles D; Haller, Daniel G et al. (2018) A Phase II Study of Celecoxib With Irinotecan, 5-Fluorouracil, and Leucovorin in Patients With Previously Untreated Advanced or Metastatic Colorectal Cancer. Am J Clin Oncol 41:1193-1198
Lane, Ryan S; Femel, Julia; Breazeale, Alec P et al. (2018) IFN?-activated dermal lymphatic vessels inhibit cytotoxic T cells in melanoma and inflamed skin. J Exp Med 215:3057-3074
Smith, Nicholas R; Swain, John R; Davies, Paige S et al. (2018) Monoclonal Antibodies Reveal Dynamic Plasticity Between Lgr5- and Bmi1-Expressing Intestinal Cell Populations. Cell Mol Gastroenterol Hepatol 6:79-96
Langer, E M; Kendsersky, N D; Daniel, C J et al. (2018) ZEB1-repressed microRNAs inhibit autocrine signaling that promotes vascular mimicry of breast cancer cells. Oncogene 37:1005-1019
Sorace, Anna G; Partridge, Savannah C; Li, Xia et al. (2018) Distinguishing benign and malignant breast tumors: preliminary comparison of kinetic modeling approaches using multi-institutional dynamic contrast-enhanced MRI data from the International Breast MR Consortium 6883 trial. J Med Imaging (Bellingham) 5:011019

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