The fundamental research areas of the Cell response and Regulation Program concern the biochemical mechanisms of signal transduction and the functional changes such signals induce. The major focus of this program is to understand how cells interact with their environment and how cells influence one another's function. This is a key aspect of growth control that affects metastasis and tumorigenesis. This broad Program has three subdivisions, which provides close interactions among program members. The subprograms are: 1) intracellular signal transduction, 2) cellular structure and function, 3) intercellular interactions. This Program of the Cancer Center is designed to explore new avenues of research to uncovered processes relevant to cancer tumorigenesis, and abnormal cell function. Thus, one goal of this program is to provide a sound biologic foundation for cancer-related research at the University of Utah by incorporating existing research programs and the expertise of the principal investigators into an integrated cancer-focus group. The second function of this Program is to act as an organized ancillary service for the clinical programs. The bench-to-bedside transfer of knowledge is fostered not only by the laboratory-based investigators of these physician scientists but also by their extended interaction with other basic scientists of this and other Cancer Center members. This program has 27 primary investigators, of which seven are physicians. The Departmental affiliations of Program members include Biochemistry, Biology, Bioengineering, Experimental Pathology, Human Genetics, Medicine, Oncological Sciences, Neurology, and Pharmacology and Toxicology. One member, Mark Keating, is a members of the Howard Hughes Medical Institute. Funding for these investigators arises from diverse, extramural sources that includes various institutes of the NIH, NSF, the American Chemical Society, the American Lung Association. There are over 300 publications from Program members work over the last funding period, showing that this is a productive group of investigators.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA042014-13
Application #
6334945
Study Section
Project Start
2000-07-25
Project End
2001-04-30
Budget Start
Budget End
Support Year
13
Fiscal Year
2000
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Tavtigian, Sean V; Greenblatt, Marc S; Harrison, Steven M et al. (2018) Modeling the ACMG/AMP variant classification guidelines as a Bayesian classification framework. Genet Med 20:1054-1060
Rogers, R Aaron; Fleming, Aaron M; Burrows, Cynthia J (2018) Unusual Isothermal Hysteresis in DNA i-Motif pH Transitions: A Study of the RAD17 Promoter Sequence. Biophys J 114:1804-1815
Rogers, R Aaron; Fleming, Aaron M; Burrows, Cynthia J (2018) Rapid Screen of Potential i-Motif Forming Sequences in DNA Repair Gene Promoters. ACS Omega 3:9630-9635
Wei, Xiaomu; Calvo-Vidal, M Nieves; Chen, Siwei et al. (2018) Germline Lysine-Specific Demethylase 1 (LSD1/KDM1A) Mutations Confer Susceptibility to Multiple Myeloma. Cancer Res 78:2747-2759
Sample, Danielle C; Samadder, N Jewel; Pappas, Lisa M et al. (2018) Variables affecting penetrance of gastric and duodenal phenotype in familial adenomatous polyposis patients. BMC Gastroenterol 18:115
Barrott, Jared J; Illum, Benjamin E; Jin, Huifeng et al. (2018) Paracrine osteoprotegerin and ?-catenin stabilization support synovial sarcomagenesis in periosteal cells. J Clin Invest 128:207-218
Madsen, Michael J; Knight, Stacey; Sweeney, Carol et al. (2018) Reparameterization of PAM50 Expression Identifies Novel Breast Tumor Dimensions and Leads to Discovery of a Genome-Wide Significant Breast Cancer Locus at 12q15. Cancer Epidemiol Biomarkers Prev 27:644-652
Delker, Don A; Wood, Austin C; Snow, Angela K et al. (2018) Chemoprevention with Cyclooxygenase and Epidermal Growth Factor Receptor Inhibitors in Familial Adenomatous Polyposis Patients: mRNA Signatures of Duodenal Neoplasia. Cancer Prev Res (Phila) 11:4-15
Trott, Daniel W; Henson, Grant D; Ho, Mi H T et al. (2018) Age-related arterial immune cell infiltration in mice is attenuated by caloric restriction or voluntary exercise. Exp Gerontol 109:99-107
Wu, Yelena P; Parsons, Bridget G; Mooney, Ryan et al. (2018) Barriers and Facilitators to Melanoma Prevention and Control Behaviors Among At-Risk Children. J Community Health 43:993-1001

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