This program-project grant seeks and enhanced understanding of the nature of the carcinogenic processes induced by chemicals. Three of the projects are directed primarily toward a better understanding of events related to the initiation of tumors by chemicals, two will provide a better understanding of the post- initiation stages of carcinogenesis, and the sixth has implications for both the initiation and post-initiation stages. The studies in the Millers' laboratory are directed particularly toward the identification of the electrophilic metabolites of chemical carcinogens that are of major importance to specific carcinogenic process and to the characterization of the reaction products of these metabolites with cellular macromolecules, especially DNA. Dr. Kasper's studies will provide a better biochemical understanding of the structures of the cytochromes P-450, NADPH-cytochrome P-450 oxidoreductase, and epoxide hydrolase and of the regulation of their activities in vivo at both the transcriptional and translational levels. These data are of great importance in view of the involvement of these enzymes in the activation and/or deactivation of a wide variety of chemical carcinogens. Dr. Fahl's research seeks a detailed understanding of the role of glutathione S-transferase-catalyzed reactions in reducing the effective levels of electrophiles formed from carcinogens in target cells and in thereby decreasing the susceptibility of the cells to mutagenesis or carcinogenesis. Dr Drinkwater is exploring genetic factors that predispose mice to the development of gross hepatomas through enhancing the rate of growth of microscopic foci of enzyme-altered cells and/or hepatomas. Dr. Pitot will analyze sequential changes in enzyme- altered hepatocytes during the progression stage of rat hepatocarcinogenesis. He will also study the regulation of transcription and the stability of specific mRNAs in hepatocytes. Dr. Poland will search for variants of the Ah receptor in human lymphoblastoid cell lines and examine the functional significance of these variants. This integrated research program will utilize chemical, biochemical, molecular biological, and biological approaches to develop a better understanding of chemical carcinogenesis.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA022484-14
Application #
3092998
Study Section
Cancer Special Program Advisory Committee (CAK)
Project Start
1978-04-01
Project End
1993-03-31
Budget Start
1991-04-01
Budget End
1992-03-31
Support Year
14
Fiscal Year
1991
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
Schools of Medicine
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Xia, Chuanwu; Rwere, Freeborn; Im, Sangchoul et al. (2018) Structural and Kinetic Studies of Asp632 Mutants and Fully Reduced NADPH-Cytochrome P450 Oxidoreductase Define the Role of Asp632 Loop Dynamics in the Control of NADPH Binding and Hydride Transfer. Biochemistry 57:945-962
Oberley, Christopher C; Bilger, Andrea; Drinkwater, Norman R (2015) Genetic background determines if Stat5b suppresses or enhances murine hepatocarcinogenesis. Mol Carcinog 54:959-70
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Xia, Chuanwu; Hamdane, Djemel; Shen, Anna L et al. (2011) Conformational changes of NADPH-cytochrome P450 oxidoreductase are essential for catalysis and cofactor binding. J Biol Chem 286:16246-60
Stein, Timothy J; Jochem, Adam; Holmes, Katie E et al. (2011) Effect of mutant ?-catenin on liver growth homeostasis and hepatocarcinogenesis in transgenic mice. Liver Int 31:303-12
Copp, Richard R; Peebles, Daniel D; Fahl, William E (2011) Synthesis and growth regulatory activity of a prototype member of a new family of aminothiol radioprotectors. Bioorg Med Chem Lett 21:7426-30
Figueiredo, Marxa L; Wentworth, Kristin M; Sandgren, Eric P (2010) Quantifying growth and transformation frequency of oncogene-expressing mouse hepatocytes in vivo. Hepatology 52:634-43

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