The Radiation and Free Radical Research Core (RFRRC) has been in operation since 1947, and became a developing HCCC core in 2000. The core progressed to a full HCCC-supported shared resource in 2005. It is directed by Dr. Douglas Spitz, who together with co-directors Drs. Frederick Domann, Garry Buettner, and Prabhat Goswami, oversees all core operations. All have considerable experience and international reputations in free radical-focused cancer research. The overall goal of the RFRRC is to provide state-of-the-art technologies to HCCC investigators doing both basic and translational studies, encompassing the roles of metabolic oxidative stress and redox signaling in cancer biology and therapy. The three basic services provided by this shared research resource are: 1) Ionizing radiation services, phosphorimaging, and cell-cycle analytical tools critical to understanding basic cellular behavior and responses to radiation and chemotherapy. 2) Electron paramagnetic resonance spectroscopy and other analytical chemistry detection methodologies for measuring free radicals, singlet oxygen, small molecule antioxidants, nitric oxide and the array of related oxidants and oxidative damage products. 3) Antioxidant enzyme services to provide easy access to technologies for modifying and measuring molecules responsible for pro-oxidant formation and oxidative damage. Major equipment available in the RFRRC includes several radiation sources, a Seahorse analyzer, various types of spectrophotometers, hypoxia chambers, and equipment for HPLC separation and analyte detection. The RFRRC provides HCCC members with easy access to specialized knowledge, reagents, equipment and resources in a highly collaborative and helpful environment. In the past calendar year, 40 HCCC members from all 4 Programs utilized this shared research resource. The long term goal of the RFRRC is to continue to facilitate research involving all aspects of redox cancer biology in the HCCC (and at other cancer centers nationally) for the purpose of developing novel analytic and therapeutic approaches, based on fundamental differences in oxidative metabolism in cancer cells.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Center Core Grants (P30)
Project #
2P30CA086862-16
Application #
9072954
Study Section
Subcommittee I - Transistion to Independence (NCI)
Project Start
Project End
Budget Start
2016-04-01
Budget End
2017-03-31
Support Year
16
Fiscal Year
2016
Total Cost
Indirect Cost
Name
University of Iowa
Department
Type
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52246
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Brandt, Kristin E; Falls, Kelly C; Schoenfeld, Joshua D et al. (2018) Augmentation of intracellular iron using iron sucrose enhances the toxicity of pharmacological ascorbate in colon cancer cells. Redox Biol 14:82-87

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