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 #
5P30CA042014-14
Application #
6484694
Study Section
Project Start
2001-08-03
Project End
2002-04-30
Budget Start
Budget End
Support Year
14
Fiscal Year
2001
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Vahrenkamp, Jeffery M; Yang, Chieh-Hsiang; Rodriguez, Adriana C et al. (2018) Clinical and Genomic Crosstalk between Glucocorticoid Receptor and Estrogen Receptor ? In Endometrial Cancer. Cell Rep 22:2995-3005
Gupta, Sumati; Albertson, Daniel; Gaston, David et al. (2018) Comprehensive Genomic Sequencing of Urothelial Tumors Identifies Rare SMARCB1 (INI-1)-Deficient Carcinomas of the Urinary System. Clin Genitourin Cancer 16:e373-e382
Yazdimamaghani, Mostafa; Moos, Philip J; Ghandehari, Hamidreza (2018) Global gene expression analysis of macrophage response induced by nonporous and porous silica nanoparticles. Nanomedicine 14:533-545
Al-Agha, Abdulmoein Eid; Ahmed, Ihab Abdulhamed; Nuebel, Esther et al. (2018) Primary Ovarian Insufficiency and Azoospermia in Carriers of a Homozygous PSMC3IP Stop Gain Mutation. J Clin Endocrinol Metab 103:555-563
Petersen, Jenna; Koptiuch, Cathryn; Wu, Yelena P et al. (2018) Patterns of family communication and preferred resources for sharing information among families with a Lynch syndrome diagnosis. Patient Educ Couns 101:2011-2017
Flack, Caralyn E; Parkinson, John S (2018) A zipped-helix cap potentiates HAMP domain control of chemoreceptor signaling. Proc Natl Acad Sci U S A 115:E3519-E3528
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
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
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

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