Literature DB >> 18821782

Identification of adducts formed in the reactions of 5'-acetoxy-N'-nitrosonornicotine with deoxyadenosine, thymidine, and DNA.

Pramod Upadhyaya1, Stephen S Hecht.   

Abstract

N'-Nitrosonornicotine (NNN) is the most prevalent of the carcinogenic tobacco-specific nitrosamines found in all tobacco products. Previous studies have demonstrated that cytochrome P450-mediated 5'-hydroxylation of NNN is a major metabolic pathway leading to mutagenic products, but to date, DNA adducts formed by this pathway have been only partially characterized, and there have been no studies reported on adducts formed with bases other than dGuo. Because adducts with dAdo and dThd have been identified in the DNA of the livers of rats treated with the structurally related carcinogen N-nitrosopyrrolidine, we investigated dAdo and dThd adduct formation from 5'-acetoxyNNN (3), a stable precursor to 5'-hydroxyNNN (2). Reaction of 3 with dAdo gave diastereomeric products, which were identified by their spectral properties and LC-ESI-MS/MS-SRM analysis as N(6)-[5-(3-pyridyl)tetrahydrofuran-2-yl]dAdo (9). This adduct was further characterized by NaBH(3)CN reduction to N(6)-[4-hydroxy-4-(3-pyridyl)but-1-yl]dAdo (17). A second dAdo adduct was identified, after NaBH(3)CN treatment, as 6-[2-(3-pyridyl)pyrrolidin-1-yl]purine-2'-deoxyriboside (18). Reaction of 3 with dThd, followed by NaBH(3)CN reduction, gave O(2)-[4-(3-pyridyl)-4-hydroxybut-1-yl]thymidine (11). Adducts 9, 11, 17, and 18 were all identified by LC-ESI-MS/MS-SRM comparison to synthetic standards. The reaction of 3 with calf thymus DNA was then investigated. The DNA was enzymatically hydrolyzed to deoxyribonucleosides, and the resulting mixture was treated with NaBH(3)CN and analyzed by LC-ESI-MS/MS-SRM. Adducts 11, 17, and 18, as well as the previously identified dGuo adducts, were identified. The results of this study provide a more comprehensive picture of DNA adduct formation by the quantitatively important 5'-hydroxylation pathway of NNN and will facilitate investigation of the presence of these adducts in laboratory animals treated with NNN or in people who use tobacco products.

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Year:  2008        PMID: 18821782      PMCID: PMC2646895          DOI: 10.1021/tx8002559

Source DB:  PubMed          Journal:  Chem Res Toxicol        ISSN: 0893-228X            Impact factor:   3.739


  27 in total

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Journal:  Chem Res Toxicol       Date:  1998-06       Impact factor: 3.739

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Journal:  Cancer Res       Date:  1978-11       Impact factor: 12.701

3.  Comparative metabolism of the tobacco-related carcinogens benzo[a]pyrene, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol, and N'- nitrosonornicotine in human hepatic microsomes.

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Journal:  Drug Metab Dispos       Date:  1997-02       Impact factor: 3.922

4.  Metabolism and pharmacokinetics of N'-nitrosonornicotine in the patas monkey.

Authors:  Pramod Upadhyaya; Cheryl L Zimmerman; Stephen S Hecht
Journal:  Drug Metab Dispos       Date:  2002-10       Impact factor: 3.922

5.  Identification of O2-substituted pyrimidine adducts formed in reactions of 4-(acetoxymethylnitrosamino)- 1-(3-pyridyl)-1-butanone and 4-(acetoxymethylnitros- amino)-1-(3-pyridyl)-1-butanol with DNA.

Authors:  Stephen S Hecht; Peter W Villalta; Shana J Sturla; Guang Cheng; Nanxiong Yu; Pramod Upadhyaya; Mingyao Wang
Journal:  Chem Res Toxicol       Date:  2004-05       Impact factor: 3.739

6.  Induction of oral cavity tumors in F344 rats by tobacco-specific nitrosamines and snuff.

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Journal:  Cancer Res       Date:  1986-08       Impact factor: 12.701

Review 7.  Tobacco-specific nitrosamines, an important group of carcinogens in tobacco and tobacco smoke.

Authors:  S S Hecht; D Hoffmann
Journal:  Carcinogenesis       Date:  1988-06       Impact factor: 4.944

8.  Dose-response study of the carcinogenicity of tobacco-specific N-nitrosamines in F344 rats.

Authors:  D Hoffmann; A Rivenson; S Amin; S S Hecht
Journal:  J Cancer Res Clin Oncol       Date:  1984       Impact factor: 4.553

9.  Mass spectrometric analysis of tobacco-specific nitrosamine-DNA adducts in smokers and nonsmokers.

Authors:  P G Foiles; S A Akerkar; S G Carmella; M Kagan; G D Stoner; J H Resau; S S Hecht
Journal:  Chem Res Toxicol       Date:  1991 May-Jun       Impact factor: 3.739

Review 10.  Human urinary carcinogen metabolites: biomarkers for investigating tobacco and cancer.

Authors:  Stephen S Hecht
Journal:  Carcinogenesis       Date:  2002-06       Impact factor: 4.944

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  9 in total

1.  Quantitation of pyridyloxobutyl-DNA adducts in tissues of rats treated chronically with (R)- or (S)-N'-nitrosonornicotine (NNN) in a carcinogenicity study.

Authors:  Lijiao Zhao; Silvia Balbo; Mingyao Wang; Pramod Upadhyaya; Samir S Khariwala; Peter W Villalta; Stephen S Hecht
Journal:  Chem Res Toxicol       Date:  2013-09-18       Impact factor: 3.739

2.  Analysis and Identification of 2'-Deoxyadenosine-Derived Adducts in Lung and Liver DNA of F-344 Rats Treated with the Tobacco-Specific Carcinogen 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanone and Enantiomers of its Metabolite 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol.

Authors:  Erik S Carlson; Pramod Upadhyaya; Peter W Villalta; Bin Ma; Stephen S Hecht
Journal:  Chem Res Toxicol       Date:  2018-04-19       Impact factor: 3.739

3.  Interstrand DNA-DNA cross-link formation between adenine residues and abasic sites in duplex DNA.

Authors:  Nathan E Price; Kevin M Johnson; Jin Wang; Mostafa I Fekry; Yinsheng Wang; Kent S Gates
Journal:  J Am Chem Soc       Date:  2014-02-20       Impact factor: 15.419

Review 4.  Evolution of research on the DNA adduct chemistry of N-nitrosopyrrolidine and related aldehydes.

Authors:  Stephen S Hecht; Pramod Upadhyaya; Mingyao Wang
Journal:  Chem Res Toxicol       Date:  2011-04-21       Impact factor: 3.739

Review 5.  Metabolism and DNA Adduct Formation of Tobacco-Specific N-Nitrosamines.

Authors:  Yupeng Li; Stephen S Hecht
Journal:  Int J Mol Sci       Date:  2022-05-04       Impact factor: 6.208

6.  Formation, repair, and genotoxic properties of bulky DNA adducts formed from tobacco-specific nitrosamines.

Authors:  Lisa A Peterson
Journal:  J Nucleic Acids       Date:  2010-09-05

7.  Quantitation of pyridyloxobutyl DNA adducts in nasal and oral mucosa of rats treated chronically with enantiomers of N'-nitrosonornicotine.

Authors:  Siyi Zhang; Mingyao Wang; Peter W Villalta; Bruce R Lindgren; Yanbin Lao; Stephen S Hecht
Journal:  Chem Res Toxicol       Date:  2009-05       Impact factor: 3.739

8.  DNA Adduct Formation from Metabolic 5'-Hydroxylation of the Tobacco-Specific Carcinogen N'-Nitrosonornicotine in Human Enzyme Systems and in Rats.

Authors:  Adam T Zarth; Pramod Upadhyaya; Jing Yang; Stephen S Hecht
Journal:  Chem Res Toxicol       Date:  2016-02-09       Impact factor: 3.739

9.  Identification of an N'-Nitrosonornicotine-Specific Deoxyadenosine Adduct in Rat Liver and Lung DNA.

Authors:  Yupeng Li; Stephen S Hecht
Journal:  Chem Res Toxicol       Date:  2021-03-11       Impact factor: 3.739

  9 in total

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