The overall goal of this Program is to advance understanding of the role played by cellular oxidative events in cancer biology and therapy. The influence of peroxidative events and experimental oxidative modulations on the biology of established tumors and the perturbations induced by treatment continue to be the focus of all projects. State-of-the-art techniques in antioxidant enzyme transfection, lipid membrane modification and analysis, radical detection by electron paramagnetic resonance (EPR), molecular biology of transcription factors and quantitation of cellular lipid peroxidation by multiple complementary approaches will be used. Four projects, each directed by established investigators in two departments, provide an integrated approach to the objectives. All projects have made progress during the 48 months of funding, including identification of superoxide dismutase as a cancer suppressor enzyme/gene, identification of a new mechanism for cancer drug resistance based on oxidation, demonstration that small molecule antioxidants protect membranes from oxidative stress of anticancer drugs, emphasis on bis-allylic positions as determinant of membranes and lipid oxidative susceptibility, and demonstration that apoptosis in HL60 cells requires a peroxidase. The proposed funding period will be characterized by emphasis on in vivo transfection studies, the role of nitric oxide in cancer therapy, a new estimation of cellular oxidative state, transcription factors, and the mechanism of apoptosis. The overall structure of the Program is similar to the last submission, The interaction of the projects is extensive. The Cores will continue to provide state-of-the-art expertise. In summary, this Program will take advantage of the natural interactions of the investigators in four related projects, each utilizing two scientific cores, to solve the important and underinvestigated role of oxidation and lipids in cancer therapeutics.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA066081-08
Application #
6752041
Study Section
Subcommittee G - Education (NCI)
Program Officer
Lees, Robert G
Project Start
1996-04-05
Project End
2006-06-30
Budget Start
2004-07-01
Budget End
2005-06-30
Support Year
8
Fiscal Year
2004
Total Cost
$1,573,172
Indirect Cost
Name
University of Iowa
Department
Radiation-Diagnostic/Oncology
Type
Schools of Medicine
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
Khoo, Nicholas K H; Hebbar, Sachin; Zhao, Weiling et al. (2013) Differential activation of catalase expression and activity by PPAR agonists: implications for astrocyte protection in anti-glioma therapy. Redox Biol 1:70-9
Carr, Wanakee J; Oberley-Deegan, Rebecca E; Zhang, Yuping et al. (2011) Antioxidant proteins and reactive oxygen species are decreased in a murine epidermal side population with stem cell-like characteristics. Histochem Cell Biol 135:293-304
Du, J; Liu, J; Smith, B J et al. (2011) Role of Rac1-dependent NADPH oxidase in the growth of pancreatic cancer. Cancer Gene Ther 18:135-43
Sun, Wenqing G; Weydert, Christine J; Zhang, Yuping et al. (2010) Superoxide Enhances the Antitumor Combination of AdMnSOD Plus BCNU in Breast Cancer. Cancers (Basel) 2:68-87
Simons, Andrean L; Mattson, David M; Dornfeld, Ken et al. (2009) Glucose deprivation-induced metabolic oxidative stress and cancer therapy. J Cancer Res Ther 5 Suppl 1:S2-6
Aykin-Burns, NĂ¹khet; Ahmad, Iman M; Zhu, Yueming et al. (2009) Increased levels of superoxide and H2O2 mediate the differential susceptibility of cancer cells versus normal cells to glucose deprivation. Biochem J 418:29-37
Sun, Wenqing; Kalen, Amanda L; Smith, Brian J et al. (2009) Enhancing the antitumor activity of adriamycin and ionizing radiation. Cancer Res 69:4294-300
Du, Changbin; Gao, Zhen; Venkatesha, Venkatasubbaiah A et al. (2009) Mitochondrial ROS and radiation induced transformation in mouse embryonic fibroblasts. Cancer Biol Ther 8:1962-71
Weydert, Christine J; Zhang, Yuping; Sun, Wenqing et al. (2008) Increased oxidative stress created by adenoviral MnSOD or CuZnSOD plus BCNU (1,3-bis(2-chloroethyl)-1-nitrosourea) inhibits breast cancer cell growth. Free Radic Biol Med 44:856-67
Coleman, Mitchell C; Asbury, Carla R; Daniels, David et al. (2008) 2-deoxy-D-glucose causes cytotoxicity, oxidative stress, and radiosensitization in pancreatic cancer. Free Radic Biol Med 44:322-31

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