Preventing cancer and reducing cancer morbidity and mortality are the unifying long-range goals of the Cancer Control and Population Sciences (CCPS) Program. This Program's shared vision is to generate outstanding science that improves cancer prevention and care through bold discovery and applications. Investigative work is within two broad areas: cancer genetics and epidemiology and behavioral and outcomes research. Research in both thematic areas aims at identifying efficient intervention targets and effective intervention techniques, including individualized and patient-centric approaches along the cancer control continuum. The following are key areas of programmatic strength and depth: ? Genetic risk prediction and gene localization/discovery ? The study of gene-environment interactions ? Development and testing of models for translation of discoveries into interventions, with the goal of assuring quality implementation and broad access The CCPS Program has made considerable progress in addressing its scientific and programmatic goals during the previous five years. Recent major scientific discoveries include 1) localization and discovery of predisposing genes for prostate cancer and melanoma, 2) seminal work on the role of gene-environment interactions involving inflammatory and metabolic pathways in breast and colorectal cancer etiology, and 3) characterization of behavioral and psychosocial outcomes of genetic risk communication interventions for hereditary breast and ovarian cancer and for melanoma. Led by Anita Kinney, PhD, RN, the CCPS Program includes 32 members from five schools/colleges and 12 departments. Between July 2003 and March 2009, this highly productive and collaborative group generated 443 cancer-relevant publications, of which 25% were intra- and 20% were inter-programmatic collaborations. Program direct cost peer-reviewed funding in 2008 was $11M, including $7.3M in NCI funding. The synergistic relationship between the Cancer Center and the CCPS Program is highly beneficial to both groups. CCPS members provide methodological expertise in both basic and applied research and participate in translational research activities that bridge basic discoveries with clinical and population applications. The Cancer Center provides appropriate supportive funding, access to Shared Resources and other Center facilities, facilitation of transdisciplinary collaborations, and funding for faculty recruitments. Over the next five years, CCPS anticipates facilitating more individualized approaches to cancer prevention and treatment through relevant research findings. In addition, CCPS foresees its research in prevention and control will lead to new discoveries aimed at reducing cancer disparities among underserved populations, including American Indian, Hispanic/Latino, elderiy, and rural peoples.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
5P30CA042014-25
Application #
8661125
Study Section
Subcommittee G - Education (NCI)
Project Start
Project End
Budget Start
2014-05-01
Budget End
2015-04-30
Support Year
25
Fiscal Year
2014
Total Cost
$33,462
Indirect Cost
$19,956
Name
University of Utah
Department
Type
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Wu, Yelena P; Aspinwall, Lisa G; Nagelhout, Elizabeth et al. (2018) Development of an Educational Program Integrating Concepts of Genetic Risk and Preventive Strategies for Children with a Family History of Melanoma. J Cancer Educ 33:774-781
Pishas, Kathleen I; Drenberg, Christina D; Taslim, Cenny et al. (2018) Therapeutic Targeting of KDM1A/LSD1 in Ewing Sarcoma with SP-2509 Engages the Endoplasmic Reticulum Stress Response. Mol Cancer Ther 17:1902-1916
Blackburn, Brenna E; Ganz, Patricia A; Rowe, Kerry et al. (2018) Reproductive and gynecological complication risks among thyroid cancer survivors. J Cancer Surviv 12:702-711
Ye, Zhizhou; Ayer, Donald E (2018) Ras Suppresses TXNIP Expression by Restricting Ribosome Translocation. Mol Cell Biol :
Kim, Hyung-Seok; McKnite, Autumn; Xie, Yuanyuan et al. (2018) Fibronectin type III and intracellular domains of Toll-like receptor 4 interactor with leucine-rich repeats (Tril) are required for developmental signaling. Mol Biol Cell 29:523-531
Spiker, William Ryan; Brodke, Darrel S; Goz, Vadim et al. (2018) Evidence of an Inherited Predisposition for Spinal Cord Tumors. Global Spine J 8:340-344
Faham, Najme; Zhao, Ling; Welm, Alana L (2018) mTORC1 is a key mediator of RON-dependent breast cancer metastasis with therapeutic potential. NPJ Breast Cancer 4:36
Fuller, Andrew K; Bice, Benjamin D; Venancio, Ashlee R et al. (2018) A Method to Define the Effects of Environmental Enrichment on Colon Microbiome Biodiversity in a Mouse Colon Tumor Model. J Vis Exp :
Wang, Sophia S; Carrington, Mary; Berndt, Sonja I et al. (2018) HLA Class I and II Diversity Contributes to the Etiologic Heterogeneity of Non-Hodgkin Lymphoma Subtypes. Cancer Res 78:4086-4096
Rengifo-Cam, William; Shepherd, Hailey M; Jasperson, Kory W et al. (2018) Colon Pathology Characteristics in Li-Fraumeni Syndrome. Clin Gastroenterol Hepatol 16:140-141

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