EXPERIMENTAL THERAPEUTICS PROGRAM ABSTRACT The Experimental Therapeutics (ET) Program at Huntsman Cancer Institute (HCI) is the hub that connects and coordinates discoveries made in the basic sciences with translational research and clinical trials to improve diagnostics, disease management, and treatment outcomes for cancer patients. This broad-reaching program coordinates faculty from numerous and diverse departments conducting research on mechanisms underlying normal and abnormal cellular biochemistry, physiology, pharmacology, and molecular and cell biology with physician-scientists and clinical researchers. The overarching goal is to improve patient outcomes by identifying and validating novel treatment approaches, fostering translational research to adapt laboratory observations into novel interventions, and conducting clinical research to assess the effectiveness of new treatment approaches in humans. ET Program Aims encompass discovery and translation of HCI research into clinical practice through development of novel treatment interventions, original investigator-initiated trials (IITs), industry trials (including first-in-human trials), and trials in cooperation with the National Cancer Trials Network (NCTN), all with special emphasis on cancers of particular relevance in HCI?s catchment area?the State of Utah.
The Specific Aims are: 1) to develop new cancer therapies based on discoveries from HCI science, and 2) to develop innovative treatment interventions and conduct translational and clinical research, with special emphasis on cancers relevant to HCI?s catchment area. The ET Program?s 59 members belong to 15 departments within three University of Utah schools/colleges. Peer-reviewed cancer-related funding was $4.9M at the end of 2018, with $2.6M (53%) of that from the National Cancer Institute. Program members also hold $9.8M in industry funding. During the previous cycle, ET members published 970 peer-reviewed cancer research papers. Of these, 20% resulted from intra- programmatic collaborations, while 23% represent inter-programmatic collaborations. Further, the Program houses 288 interventional treatment trials that accrued 676 patients in 2018. The ET Program is instrumental to the success of HCI?s overall mission to improve the outcomes of cancer patients. In particular, we: 1) translate deep basic mechanistic understandings and pioneering preclinical translational research into original clinical trials, and 2) collect and conduct iterative analysis of specimens from patients on clinical trials to improve our understanding of disease mechanisms and therapeutic sensitivity or resistance in human beings. Going forward, the ET Program will strive to bring research full circle to fuel a virtuous cycle of discovery, preclinical translation, clinical testing, and bedside-to-bench analyses.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA042014-31
Application #
9935887
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2020-04-01
Budget End
2021-03-31
Support Year
31
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
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
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
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
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
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 :

Showing the most recent 10 out of 1193 publications