Oxidative genomic damage in humans exposed to high indoor radon levels in Northeast Brazil.

Autor: da Costa Xavier LA; Post-graduation Program of Biochemistry and Molecular Biology, Laboratory of Toxicological Genetic, Federal University of Rio Grande do Norte, Natal, RN, Brazil., Navoni JA; Post-graduation Program of Development and Environment - DDMA, Federal University of Rio Grande do Norte (UFRN), Natal/RN, Brazil., Souza do Amaral V; Post-graduation Program of Biochemistry and Molecular Biology, Laboratory of Toxicological Genetic, Federal University of Rio Grande do Norte, Natal, RN, Brazil; Post-graduation Program of Development and Environment - DDMA, Federal University of Rio Grande do Norte (UFRN), Natal/RN, Brazil.. Electronic address: vi.mariga@gmail.com.
Jazyk: angličtina
Zdroj: Mutation research. Genetic toxicology and environmental mutagenesis [Mutat Res Genet Toxicol Environ Mutagen] 2023 Jul; Vol. 889, pp. 503652. Date of Electronic Publication: 2023 Jun 23.
DOI: 10.1016/j.mrgentox.2023.503652
Abstrakt: Radon gas inhalation is the main source of exposure to ionizing radiation by humans. There is still lack in knowledge concerning the chronic and indirect effects of exposure to this carcinogenic factor. Therefore, the aim of this work is to analyze the levels of oxidative genomic damage in inhabitants of a medium-high background radiation area (HBRA) (N = 82) in Northeastern Brazil and compare them with people living in a low background radiation area (LBRA) (N = 46). 8-hydroxy-2-deoxyguanosine (8-OHdG) was quantified in urine, Ser326Cys polymorphism was determined in the hOGG1 gene and indoor radon was measured. HBRA houses had 6.5 times higher indoor radon levels than those from LBRA (p-value < 0.001). The 8-OHdG mean (95% confidence interval) were significantly different, 8.42 (5.98-11.9) ng/mg creatinine and 29.91 (23.37-38.30) ng/mg creatinine for LBRA and HBRA, respectively. The variables representing lifestyle and environmental and occupational exposures did not have a significant association with oxidized guanosine concentrations. On the other hand, lower 8-OHdG values were observed in subjects that had one mutant allele (326Cys) in the hOGG1 gene than those who had both wild alleles (Ser/Ser (p-value < 0.05). It can be concluded that high radon levels have significantly influenced the genome oxidative metabolism and hOGG1 gene polymorphism would mediate the observed biological response.
Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.
(Copyright © 2023 Elsevier B.V. All rights reserved.)
Databáze: MEDLINE
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