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DNA damage in oral epithelial cells of individuals chronically exposed to indoor radon (222Rn) in a hydrothermal area
Authors:Diana Paula Silva Linhares  Patrícia Ventura Garcia  Catarina Silva  Joana Barroso  Nadya Kazachkova  Rui Pereira  Manuela Lima  Ricardo Camarinho  Teresa Ferreira  Armindo dos Santos Rodrigues
Affiliation:1.Department of Biology,University of the Azores,Ponta Delgada,Portugal;2.cE3c, Centre for Ecology Evolution and Environmental Changes and Azorean Biodiversity Group,University of the Azores,Ponta Delgada,Portugal;3.Department of Geosciences,University of the Azores,Ponta Delgada,Portugal;4.CVARG, Center for Volcanology and Geological Risks Assessment,University of the Azores,Ponta Delgada,Portugal;5.CIVISA, Center for Information and Seismovolcanic Surveillance of the Azores,University of the Azores,Ponta Delgada,Portugal;6.Instituto de Investiga??o e Inova??o em Saúde,Universidade do Porto,Porto,Portugal;7.Institute for Molecular and Cell Biology (IBMC),University of Porto,Porto,Portugal
Abstract:Hydrothermal areas are potentially hazardous to humans as volcanic gases such as radon (222Rn) are continuously released from soil diffuse degassing. Exposure to radon is estimated to be the second leading cause of lung cancer, but little is known about radon health-associated risks in hydrothermal regions. This cross-sectional study was designed to evaluate the DNA damage in the buccal epithelial cells of individuals chronically exposed to indoor radon in a volcanic area (Furnas volcano, Azores, Portugal) with a hydrothermal system. Buccal epithelial cells were collected from 33 individuals inhabiting the hydrothermal area (Ribeira Quente village) and from 49 individuals inhabiting a non-hydrothermal area (Ponta Delgada city). Indoor radon was measured with Ramon 2.2 detectors. Chromosome damage was measured by micronucleus cytome assay, and RAPD-PCR was used as a complementary tool to evaluate DNA damage, using three 10-mer primers (D11, F1 and F12). Indoor radon concentration correlated positively with the frequency of micronucleated cells (r s = 0.325, p = 0.003). Exposure to radon is a risk factor for the occurrence micronucleated cells in the inhabitants of the hydrothermal area (RR = 1.71; 95% CI, 1.2–2.4; p = 0.003). One RAPD-PCR primer (F12) produced differences in the banding pattern, a fact that can indicate its potential for detecting radon-induced specific genomic alterations. The observed association between chronic exposure to indoor radon and the occurrence of chromosome damage in human oral epithelial cells evidences the usefulness of biological surveillance to assess mutations involved in pre-carcinogenesis in hydrothermal areas, reinforcing the need for further studies with human populations living in these areas.
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