Cytogenetic biomonitoring of inhabitants of a large uranium mineralization area: the municipalities of Monte Alegre, Prainha, and Alenquer, in the State of Para, Brazil


Autoria(s): GUIMARAES, Adriana Costa; ANTUNES, Lusania Maria Greggi; RIBEIRO, Helem Ferreira; SANTOS, Andrea Kelly Ribeiro dos; CARDOSO, Plinio Cerqueira dos Santos; LIMA, Patricia Lima de; SEABRA, Aline Damasceno; PONTES, Thais Brilhante; PESSOA, Claudia; MORAES, Manoel Odorico de; CAVALCANTI, Bruno Coelho; SOMBRA, Carla Maria Lima; BAHIA, Marcelo de Oliveira; BURBANO, Rommel Rodriguez
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2010

Resumo

Uranium is a natural radioactive metallic element; its effect on the organism is cumulative, and chronic exposure to this element can induce carcinogenesis. Three cities of the Amazon region-Monte Alegre, Prainha, and Alenquer-in North Brazil, are located in one of the largest uranium mineralization areas of the world. Radon is a radioactive gas, part of uranium decay series and readily diffuses through rock. In Monte Alegre, most of the houses are built of rocks removed from the Earth`s crust in the forest, where the uranium reserves lie. The objective of the present work is to determine the presence or absence of genotoxicity and risk of carcinogenesis induced by natural exposure to uranium and radon in the populations of these three cities. The frequency of micronuclei (MN) and chromosomal aberrations (CA) showed no statistically significant differences between the control population and the three study populations (P > 0.05). MN was also analyzed using the fluorescence in situ hybridization (FISH) technique, with a centromere-specific probe. No clastogenic and/or aneugenic effects were found in the populations. Using FISH analysis, other carcinogenesis biomarkers were analyzed, but neither the presence of the IGH/BCL2 translocation nor an amplification of the MYC gene and 22q21 region was detected. Clastogenicity and DNA damage were also not found in the populations analyzed using the alkaline comet assay. The mitotic index showed no cytotoxicity in the analyzed individuals` lymphocytes. Once we do not have data concerning radiation doses from other sources, such as cosmic rays, potassium, thorium, or anthropogenic sources, it is hard to determine if uranium emissions in this geographic region where our study population lives are too low to cause significant DNA damage. Regardless, genetic analyses suggest that the radiation in our study area is not high enough to induce DNA alterations or to interfere with mitotic apparatus formation. It is also possible that damages caused by radiation doses undergo cellular repair.

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)[409826/206-5]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)[308256/2006-9]

Identificador

CELL BIOLOGY AND TOXICOLOGY, v.26, n.5, p.403-419, 2010

0742-2091

http://producao.usp.br/handle/BDPI/20320

10.1007/s10565-010-9152-8

http://dx.doi.org/10.1007/s10565-010-9152-8

Idioma(s)

eng

Publicador

SPRINGER

Relação

Cell Biology and Toxicology

Direitos

restrictedAccess

Copyright SPRINGER

Palavras-Chave #Populational biomonitoring #Uranium #Genotoxicity #Carcinogenesis #HUMAN OSTEOBLAST CELLS #IN-SITU HYBRIDIZATION #MICRONUCLEUS-CENTROMERE ASSAY #PERIPHERAL-BLOOD LYMPHOCYTES #INDOOR RADON CONCENTRATIONS #GULF-WAR VETERANS #DEPLETED-URANIUM #DNA-DAMAGE #CHROMOSOME-ABERRATIONS #IONIZING-RADIATION #Cell Biology #Toxicology
Tipo

article

original article

publishedVersion