Naphthalene genotoxicity: DNA adducts in primate and mouse airway explants.

Toxicol Lett

Center for Health and the Environment, University of California Davis, Davis, CA 95616, USA; Department of Anatomy, Physiology and Cell Biology, School of Veterinary Medicine, University of California Davis, Davis, CA 95616, USA. Electronic address:

Published: May 2019

AI Article Synopsis

  • The study investigates the potential of naphthalene (NA) to form DNA adducts, which are linked to cancer, in lung tissues from different species.
  • Despite low overall metabolism in primates, the research found that NA-DNA adducts were more prevalent in female mice and primates than males.
  • Additionally, a metabolic product of NA, 1,2-naphthoquinone (NQ), showed even greater potency in forming DNA adducts, indicating that NA could potentially contribute to cancer development through DNA damage.

Article Abstract

Naphthalene (NA) is a ubiquitous environmental pollutant and possible human carcinogen that forms tumors in rodents with tissue/regional and species selectivity. This study seeks to determine whether NA is able to directly adduct DNA in an ex vivo culture system. Metabolically active lung tissue was isolated and incubated in explant culture with carbon-14 labeled NA (0, 25, 250 μM) or 1,2-naphthoquinone (NQ), followed by AMS analyses of metabolite binding to DNA. Despite relatively low metabolic bioactivation in the primate airway, dose-dependent NA-DNA adduct formation was detected. More airway adducts were detected in female mice (4.7-fold) and primates (2.1-fold) than in males of the same species. Few adducts were detected in rat airway or nasal epithelium. NQ, which is a metabolic product of NA, proved to be even more potent, with levels of adduct formation 70-80-fold higher than seen when tissues were incubated with the parent compound NA. This is the first study to demonstrate NA-DNA adduct formation at a site of carcinogenesis, the mouse lung. Adducts were also detected in non-human primate lung and with a NQ metabolite of NA. Taken together, this suggests that NA may contribute to in vivo carcinogenesis through a genotoxic mechanism.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6459408PMC
http://dx.doi.org/10.1016/j.toxlet.2019.01.009DOI Listing

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