Role of oxidants in DNA damage: hydroxyl radical mediates the synergistic DNA damaging effects of asbestos and cigarette smoke

• Published in: The Journal of clinical investigation 1987-10, Vol.80 (4), p.1090-1095
• Main Authors: JACKSON, J. H, SCHRAUFSTATTER, I. U, HYSLOP, P. A, VOSBECK, K, SAUERHEBER, R, WEITZMAN, S. A, COCHRANE, C. G
• Format: Article
• Language: English
• Subjects: Asbestos - pharmacology; Bacteriophages - genetics; Benzoates - pharmacology; Benzoic Acid; Biological and medical sciences; Catalase - metabolism; Dihydropyridines - pharmacology; Dimethyl Sulfoxide - pharmacology; DNA - drug effects; Drug Synergism; Electron Spin Resonance Spectroscopy; Hydroxides; Hydroxyl Radical; Mannitol - pharmacology; Medical sciences; Nucleic Acid Conformation - drug effects; Phenanthrolines - pharmacology; Smoking; Superoxide Dismutase - metabolism; Thiazoles - pharmacology; Tobacco, tobacco smoking; Toxicology
• ISSN: 0021-9738; 1558-8238
• DOI: 10.1172/JCI113165

The mechanism by which cigarette smoking and asbestos exposure synergistically increase the incidence of lung cancer is unknown. We hypothesized that cigarette smoke and asbestos might synergistically increase DNA damage. To test this hypothesis we exposed isolated bacteriophage PM2 DNA to cigarette smoke and/or asbestos, and assessed DNA strand breaks as an index of DNA damage. Our results supported our hypothesis. 78 +/- 12% of the DNA exposed to both cigarette smoke and asbestos developed strand breaks, while only 9.8 +/- 7.0 or 4.3 +/- 3.3% of the DNA exposed to cigarette smoke or asbestos, respectively, developed strand breaks under the conditions of the experiment. Our experimental evidence suggested that cigarette smoke and asbestos synergistically increased DNA damage by stimulating .OH formation. First, significant amounts of .OH were detected by electron paramagnetic resonance (EPR) in DNA mixtures containing both cigarette smoke and asbestos, but no .OH was detected in mixtures containing cigarette smoke alone or asbestos alone. Second, the .OH scavengers, dimethylsulfoxide (DMSO), mannitol, or Na benzoate decreased both .OH detection by EPR and strand breaks in DNA mixtures exposed to cigarette smoke and asbestos. Third, the H2O2 scavenger, catalase, and the iron chelators, 1,10-phenanthroline and desferrithiocin, decreased both .OH detection and strand breaks in DNA mixtures exposed to cigarette smoke and asbestos. These latter findings suggest that iron contained in asbestos may catalyze the formation of .OH from H2O2 generated by cigarette smoke. In summary, our study indicates that cigarette smoke and asbestos synergistically increase DNA damage and suggests that this synergism may involve .OH production.