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1.
J Environ Sci (China) ; 41: 270-277, 2016 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-26969074

RESUMO

Fish from the Great Lakes contain polychlorinated biphenyls (PCBs) which have been shown to disrupt endocrine function and mimic thyroid hormones, but they also contain beneficial omega-3 fatty acids that may offer protection against endocrine cancers. The purpose of this study was to examine the effects of Lake Ontario fish consumption and the estimated consumption of PCBs and omega-3 fatty acids on the risk of thyroid cancer in a group of sport fishermen. Anglers from the New York State Angler Cohort Study were followed for cancer incidence from 1991-2008. Twenty-seven cases of incident thyroid cancer and 108 controls were included in the analyses. Total estimated fish consumption, estimated omega-3 fatty acid consumption, and estimated PCB consumption from Lake Ontario fish were examined for an association with the incidence of thyroid cancer, while matching on sex, and controlling for age and smoking status. Results from logistic regression indicate no significant associations between fish consumption, short-term estimated omega-3 fatty acids, or estimated PCB consumption from Great Lakes fish and the development of thyroid cancer, but it was suggested that long-term omega-3 fatty acid from Great Lakes fish may be protective of the development of thyroid cancer. In conclusion, fish consumption, with the possible concomitant PCBs, from the Great Lakes does not appear to increase the risk of thyroid cancer in New York anglers. Further research is needed in order to separate the individual health effects of PCBs from omega-3 fatty acids contained within the fish.


Assuntos
Exposição Ambiental , Ácidos Graxos Ômega-3/metabolismo , Peixes , Contaminação de Alimentos/análise , Bifenilos Policlorados/toxicidade , Neoplasias da Glândula Tireoide/epidemiologia , Poluentes Químicos da Água/toxicidade , Adolescente , Adulto , Idoso , Animais , Estudos de Coortes , Ácidos Graxos Ômega-3/toxicidade , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , New York/epidemiologia , Medição de Risco , Neoplasias da Glândula Tireoide/induzido quimicamente , Adulto Jovem
2.
Mutat Res ; 582(1-2): 53-60, 2005 Apr 04.
Artigo em Inglês | MEDLINE | ID: mdl-15781210

RESUMO

Experimental evidence suggests that green tea (Camellia sinesis) may reduce the risk of lung cancer through several hypothesized mechanisms including scavenging oxidative radicals, inhibition of tumor initiation, and modulation of detoxification enzymes. However, epidemiologic results have not been consistent as to the relationship between green tea consumption and lung caner prevention. We employed a population-based case-control study of 122 cases and 122 controls to investigate the effect that green tea consumption may have on the risk of lung cancer and whether polymorphisms in 8-oxoguanine-DNA glycosylase (OGG1), glutathione-S-transferase M1 (GSTM1), and aldo-keto reductase 1C3 (AKR1C3) modify such an association. Daily green tea consumption was associated with a non-significant reduction in lung cancer risk. However, the effect of smoky coal exposure was higher for non-drinkers (odds ratio (OR)=4.93; 95% confidence interval (95% CI)=1.27-19.13) than for drinkers (OR=1.88; 95% CI=1.01-3.48). Further, among individuals with the OGG1 Cys(326) allele, daily consumption was associated with a 72% reduction (95% CI=0.09-0.94). Among GSTM1 null homozygotes, those who consumed green tea daily had a non-significant reduction in risk compared with non-consumers. Green tea consumption had no effect among OGG1 Ser(326) homozygotes or GSTM1 carriers. In addition, AKR1C3 genotype did not modulate the effect of green tea consumption. The chemopreventive effects of green tea in this population may be restricted to individuals who are particularly susceptible to oxidative stress and oxidative DNA damage.


Assuntos
Carvão Mineral/análise , Predisposição Genética para Doença , Neoplasias Pulmonares/prevenção & controle , Compostos Policíclicos/análise , Chá , Oxirredutases do Álcool/genética , Aldeído Redutase , Aldo-Ceto Redutases , Estudos de Casos e Controles , DNA Glicosilases/genética , Feminino , Glutationa Transferase/genética , Humanos , Neoplasias Pulmonares/etiologia , Neoplasias Pulmonares/genética , Masculino
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