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| Research article summary (published 27 Feb 2006): |
Metabolic transformation and mechanism of action of mononitroso caffeidine- a new interpretation.
Full Abstract
Although caffeine is not carcinogenic, its hydrolysed product, caffeidine causes human cancer, possibly through endogenous nitrosation to form mononitroso caffeidine (MNC). MNC undergoes enzymatic demethylation and reacts with cellular nucleophiles, notably DNA, via the formation of a putative imidazole diazonium ion. Its interaction with proteins has not been reported. The present work is based on the hypothesis that some active metabolites of MNC covalently interact with cellular DNA and/or proteins to initiate carcinogenesis. We report here the synthesis of a possible reactive metabolite of MNC, viz., N, 1-methyl-4(N-methyl-N-nitrosamino)-imidazole-5-carboxylic acid (MNIC). Its structure has been determined by uv, ir, nmr and mass spectral analyses and its interaction with egg albumin and human serum protein has been examined by uv and CD spectroscopy. We concluded that metabolic activation of MNC occurs through the formation of MNIC. Avoiding consumption of salted tea or coffee that prevents the intake of caffeidine will possibly eliminate the risk of MNC carcinogenicity.
Author information
Author/s: Panda, G S (GS); Bhattacharya, R K (RK); Choudhuri, S K (SK);
Affiliation: Department of Environmental Carcinogenesis and Toxicology, Chittaranjan National Cancer Institute, 37 S.P.Mukherjee Road, Calcutta-700 026, India.
Journal and publication information
Publication Type: Journal Article
Journal: Endocrine, metabolic & immune disorders drug targets (Endocr Metab Immune Disord Drug Targets), published in United Arab Emirates. (Language: eng)
Reference: 2006-Mar; vol 6 (issue 1) : pp 1-6
Dates: Created 2006/04/13; Completed 2006/05/01; Revised 2007/11/15;
PMID: 16611159, status: MEDLINE (last retrieval date: 2/18/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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