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8-Hydroxydeoxyguanosine as a biomarker of oxidative DNA damage in workers exposed to low-dose benzene

The present study aims to investigate the relation between exposure to low-dose benzene and the occurrence of oxidative DNA damage in gasoline station workers, as well as the possible role of interfering or confounding factors. Urine levels of 8-OHdG were evaluated by a competitive immunoassay in a...

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Autores principales: Fenga, Concettina, Gangemi, Silvia, Teodoro, Michele, Rapisarda, Venerando, Golokhvast, Kirill, Docea, Anca Oana, Tsatsakis, Aristidis M., Costa, Chiara
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615153/
https://www.ncbi.nlm.nih.gov/pubmed/28959652
http://dx.doi.org/10.1016/j.toxrep.2017.05.008
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author Fenga, Concettina
Gangemi, Silvia
Teodoro, Michele
Rapisarda, Venerando
Golokhvast, Kirill
Docea, Anca Oana
Tsatsakis, Aristidis M.
Costa, Chiara
author_facet Fenga, Concettina
Gangemi, Silvia
Teodoro, Michele
Rapisarda, Venerando
Golokhvast, Kirill
Docea, Anca Oana
Tsatsakis, Aristidis M.
Costa, Chiara
author_sort Fenga, Concettina
collection PubMed
description The present study aims to investigate the relation between exposure to low-dose benzene and the occurrence of oxidative DNA damage in gasoline station workers, as well as the possible role of interfering or confounding factors. Urine levels of 8-OHdG were evaluated by a competitive immunoassay in a group of 80 men, employed in gasoline stations located in East Sicily and compared with a control group (n = 63) of male office employees not occupationally exposed to benzene. Information regarding socio-demographic characteristics, lifestyle and job-related records were provided through a questionnaire. Significantly higher (p < 0.05) urinary t,t,-MA and 8-OHdG levels were observed in gasoline station attendants compared to subjects not exposed to benzene. Pearson’s test demonstrated a strong correlation (r = 0.377, p < 0.001) between 8-OHdG and benzene exposure level. 8-OHdG significantly correlated also with job seniority, (r = 0.312, p < 0.01), whereas the relation with age resulted weaker (r = 0.242, p < 0.05). Multiple linear regression analysis, performed to exclude a role for confounding factors, showed that variables like gender, smoking habit, alcohol consumption and BMI did not have a significant influence on the measured biomarkers. No subject enrolled in the study presented signs or symptoms of work-related disease or other illness linked to oxidative stress. These results suggest that low-level chronic exposure to benzene among gasoline station attendants can determine oxidative damage on DNA, as indicated by alteration of 8-OHdG which may represent a non-invasive biomarker of early genotoxic damage in exposed subjects.
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spelling pubmed-56151532017-09-28 8-Hydroxydeoxyguanosine as a biomarker of oxidative DNA damage in workers exposed to low-dose benzene Fenga, Concettina Gangemi, Silvia Teodoro, Michele Rapisarda, Venerando Golokhvast, Kirill Docea, Anca Oana Tsatsakis, Aristidis M. Costa, Chiara Toxicol Rep Article The present study aims to investigate the relation between exposure to low-dose benzene and the occurrence of oxidative DNA damage in gasoline station workers, as well as the possible role of interfering or confounding factors. Urine levels of 8-OHdG were evaluated by a competitive immunoassay in a group of 80 men, employed in gasoline stations located in East Sicily and compared with a control group (n = 63) of male office employees not occupationally exposed to benzene. Information regarding socio-demographic characteristics, lifestyle and job-related records were provided through a questionnaire. Significantly higher (p < 0.05) urinary t,t,-MA and 8-OHdG levels were observed in gasoline station attendants compared to subjects not exposed to benzene. Pearson’s test demonstrated a strong correlation (r = 0.377, p < 0.001) between 8-OHdG and benzene exposure level. 8-OHdG significantly correlated also with job seniority, (r = 0.312, p < 0.01), whereas the relation with age resulted weaker (r = 0.242, p < 0.05). Multiple linear regression analysis, performed to exclude a role for confounding factors, showed that variables like gender, smoking habit, alcohol consumption and BMI did not have a significant influence on the measured biomarkers. No subject enrolled in the study presented signs or symptoms of work-related disease or other illness linked to oxidative stress. These results suggest that low-level chronic exposure to benzene among gasoline station attendants can determine oxidative damage on DNA, as indicated by alteration of 8-OHdG which may represent a non-invasive biomarker of early genotoxic damage in exposed subjects. Elsevier 2017-05-31 /pmc/articles/PMC5615153/ /pubmed/28959652 http://dx.doi.org/10.1016/j.toxrep.2017.05.008 Text en © 2017 Published by Elsevier Ireland Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Fenga, Concettina
Gangemi, Silvia
Teodoro, Michele
Rapisarda, Venerando
Golokhvast, Kirill
Docea, Anca Oana
Tsatsakis, Aristidis M.
Costa, Chiara
8-Hydroxydeoxyguanosine as a biomarker of oxidative DNA damage in workers exposed to low-dose benzene
title 8-Hydroxydeoxyguanosine as a biomarker of oxidative DNA damage in workers exposed to low-dose benzene
title_full 8-Hydroxydeoxyguanosine as a biomarker of oxidative DNA damage in workers exposed to low-dose benzene
title_fullStr 8-Hydroxydeoxyguanosine as a biomarker of oxidative DNA damage in workers exposed to low-dose benzene
title_full_unstemmed 8-Hydroxydeoxyguanosine as a biomarker of oxidative DNA damage in workers exposed to low-dose benzene
title_short 8-Hydroxydeoxyguanosine as a biomarker of oxidative DNA damage in workers exposed to low-dose benzene
title_sort 8-hydroxydeoxyguanosine as a biomarker of oxidative dna damage in workers exposed to low-dose benzene
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5615153/
https://www.ncbi.nlm.nih.gov/pubmed/28959652
http://dx.doi.org/10.1016/j.toxrep.2017.05.008
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