The most important objective in this research is to study the metabolism of N?G?-monomethyl-L-arginine, an endogenously synthesized compound, and to identify one of the metabolites as N-methylurea, a compound which can be nitrosated to give rise to 1-N-methyl,1-N-nitrosourea, one of the most potent carcinogens known. This will be pursued with the following aims: (1) to study the metabolic pathways of N?G?-monomethyl-L-arginine which involve hydrolytic cleavage, oxidative demethylation, and decarboxylation; (2) to investigate the possible formation of N-methylurea from N?G?-monomethyl-L-arginine; (3) to further purify protein methylase I which methylates the guanadine group of protein-bound arginine residues; and (4) to investigate the possible antitumor effects of N?G?-monomethyl-L-arginine on tumor cells in tissue or cell culture. (K)

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA012226-14
Application #
3163620
Study Section
Physiological Chemistry Study Section (PC)
Project Start
1976-06-01
Project End
1986-11-30
Budget Start
1984-12-01
Budget End
1985-11-30
Support Year
14
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Temple University
Department
Type
Schools of Medicine
DUNS #
City
Philadelphia
State
PA
Country
United States
Zip Code
19122
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Suh, B; Lee, H W; Hong, S Y et al. (1986) A new HPLC analytical method for o-hydroxyhippuric acid in uremic serum. J Biochem Biophys Methods 13:211-20
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Jun, G J; Ro, J Y; Kim, M H et al. (1986) Studies on the distribution of O6-methylguanine-DNA methyltransferase in rat. Biochem Pharmacol 35:377-84

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