4.2 Article

Association between mitochondrial DNA copy number, blood cell counts, and occupational benzene exposure

Journal

ENVIRONMENTAL AND MOLECULAR MUTAGENESIS
Volume 49, Issue 6, Pages 453-457

Publisher

WILEY
DOI: 10.1002/em.20402

Keywords

benzene; mitochondrial DNA; oxidative stress

Funding

  1. Intramural NIH HHS [ZIA CP010120-14, NIH0011547510] Funding Source: Medline
  2. NIEHS NIH HHS [R01 ES006721, P42 ES004705, P30ES01896, P30ES10126, P42ES04705, P30 ES001896, P42ES05948, P42 ES005948, R01ES06721, P30 ES010126] Funding Source: Medline

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Benzene is a recognized hematotoxicant and carcinogen that produces genotoxic damage. Benzene metabolites can produce reactive oxidative species. Mitochondrial DNA (mtDNA) copy number may be increased in response to oxidative stress to compensate for damaged mitochondria. We carried out a cross-sectional study of 40 benzene-exposed workers and 40 controls to evaluate the association between benzene exposure and mtDNA copy number. Copy number of mtDNA in leukocyte DNA was determined by real-time PCR. Compared with controls, the copy number of mtDNA increased by 4% and by 15% in workers exposed to <= 10 ppm (n = 20) and >10 ppm (n = 20) benzene, respectively. After adjusting for recent infection, the factor that was significantly correlated with mtDNA, the increase of mtDNA was statistically significant in the high exposed group (P = 0.016) with a significant linear trend (P = 0.024). To our best knowledge, this is the first report that benzene exposure was associated with increased mitochondria DNA copy number. Benzene exposure may induce mtDNA amplification, possibly in response to oxidative stress caused by benzene. The finding needs to be replicated by other studies.

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