Literature DB >> 19107896

Urinary levels of oxidative DNA and RNA damage among workers exposed to polycyclic aromatic hydrocarbons in silicon production: comparison with 1-hydroxypyrene.

Caroline Marie1, Jean-Luc Ravanat, Carine Badouard, Marie Marques, Franck Balducci, Anne Maître.   

Abstract

Polycyclic aromatic hydrocarbons (PAH) are ubiquitous occupational and environmental pollutants and the urinary excretion of 1-hydroxypyrene (1-OHP) is classically measured for the determination of PAH exposure internal dose. Some of PAH are tumorigenic due to their metabolites ability to generate DNA adducts and oxidative DNA damage through the production of reactive oxygen species during metabolism. 8-hydroxy-7,8-dihydro-2'-deoxyguanosine (8-OHdGuo) is one of the major oxidative DNA lesions and its use as a potential biomarker of genotoxic PAH occupational exposure should be evaluated. Indeed conflicting results are frequently reported in occupational studies in terms of correlation between 8-OHdGuo urinary levels and PAH exposure. The aim of our study was therefore to determine the potential for PAH occupational exposure to increase urinary oxidative DNA damage. The population consisted of 68 male workers employed in silicon production. The urinary concentrations of 8-OHdGuo and its homologue in RNA, 8-hydroxy-7,8-dihydroguanosine (8-OHGuo) were determined using high performance liquid chromatography (HPLC) coupled to tandem mass spectrometry, whereas those of 1-OHP were measured using HPLC with fluorescence detection. Individual variation rates were calculated on a working day and a working week. The results indicated that, while 1-OHP levels strongly increased on a working day and even more on a working week, 8-OHdGuo and 8-OHGuo urinary levels did not show similar significant increases. Moreover, no correlation between 1-OHP and oxidative DNA and RNA lesions was found. Consequently, urinary 8-OHdGuo and 8-OHGuo did not seem to be relevant biomarkers of genotoxic PAH exposure in the case of the silicon plant studied. (c) 2008 Wiley-Liss, Inc.

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Year:  2009        PMID: 19107896     DOI: 10.1002/em.20439

Source DB:  PubMed          Journal:  Environ Mol Mutagen        ISSN: 0893-6692            Impact factor:   3.216


  6 in total

Review 1.  Current perspectives on the clinical implications of oxidative RNA damage in aging research: challenges and opportunities.

Authors:  Zhijie Xu; Jinzhou Huang; Ming Gao; Guijie Guo; Shuangshuang Zeng; Xi Chen; Xiang Wang; Zhicheng Gong; Yuanliang Yan
Journal:  Geroscience       Date:  2020-06-11       Impact factor: 7.713

2.  Relevance of urinary 3-hydroxybenzo(a)pyrene and 1-hydroxypyrene to assess exposure to carcinogenic polycyclic aromatic hydrocarbon mixtures in metallurgy workers.

Authors:  Damien Barbeau; Renaud Persoons; Marie Marques; Claire Hervé; Gilbert Laffitte-Rigaud; Anne Maitre
Journal:  Ann Occup Hyg       Date:  2014-02-06

3.  An oxygenated metabolite of benzo[a]pyrene increases hepatic β-oxidation of fatty acids in chick embryos.

Authors:  Ola Westman; Maria Larsson; Nikolaos Venizelos; Henner Hollert; Magnus Engwall
Journal:  Environ Sci Pollut Res Int       Date:  2014-01-03       Impact factor: 4.223

4.  Polycyclic aromatic hydrocarbon (PAH) exposure and oxidative stress for a rural population from the North China Plain.

Authors:  Qiaoyun Yang; Xinghua Qiu; Ran Li; Jin Ma; Keqiu Li; Guang Li
Journal:  Environ Sci Pollut Res Int       Date:  2015-02       Impact factor: 4.223

5.  Biomarkers of oxidative stress and its association with the urinary reducing capacity in bus maintenance workers.

Authors:  Jean-Jacques Sauvain; Ari Setyan; Pascal Wild; Philippe Tacchini; Grégoire Lagger; Ferdinand Storti; Simon Deslarzes; Michel Guillemin; Michel J Rossi; Michael Riediker
Journal:  J Occup Med Toxicol       Date:  2011-05-30       Impact factor: 2.646

6.  The extreme variety of genotoxic response to benzo[a]pyrene in three different human cell lines from three different organs.

Authors:  Camille Genies; Anne Maître; Emmanuel Lefèbvre; Amandine Jullien; Marianne Chopard-Lallier; Thierry Douki
Journal:  PLoS One       Date:  2013-11-08       Impact factor: 3.240

  6 in total

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