The objective of this study is to employ the Azoxymethane induced rat colon tumor model to screen for potential chemopreventive agents. This model induces adenomas and carcinomas in the colons of treated F344 male rats. The resulting tumors appear histologically similar to human tumors and furthermore exhibit Ki Ras mutations in approximately 50% of tumors similarly to humans. We will examine three individual agents for their chemopreventive activity (Cox 2 inhibitor, retinoid, ODC inhibitor) as well as combinations of agents NSAIDS or ODC inhibitor plus retinoids. The latter studies are based on our recent findings that some of the retinoids appear to be effective agents in the AOM tumor model. Should any of these agents or combinations of agents prove efficaceous in this model they will be advanced for further preclinical biological and toxicologic studies prior to their development in the clinic.

Agency
National Institute of Health (NIH)
Institute
Division of Cancer Prevention And Control (NCI)
Type
Research and Development Contracts (N01)
Project #
N01CN075102-002
Application #
6312250
Study Section
Project Start
1997-06-30
Project End
2001-06-29
Budget Start
2000-05-01
Budget End
2001-06-29
Support Year
Fiscal Year
2000
Total Cost
$36,390
Indirect Cost
Name
University of Toledo
Department
Pathology
Type
Schools of Medicine
DUNS #
807418939
City
Toledo
State
OH
Country
United States
Zip Code
43614
Tao, Lianhui; Wang, Wei; Kramer, Paula M et al. (2004) Modulation of DNA hypomethylation as a surrogate endpoint biomarker for chemoprevention of colon cancer. Mol Carcinog 39:79-84
Tao, Lianhui; Kramer, Paula M; Wang, Wei et al. (2002) Altered expression of c-myc, p16 and p27 in rat colon tumors and its reversal by short-term treatment with chemopreventive agents. Carcinogenesis 23:1447-54
Gunning, W T; Kramer, P M; Lubet, R A et al. (2000) Chemoprevention of vinyl carbamate-induced lung tumors in strain A mice. Exp Lung Res 26:757-72