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Biomarkers ; 9(4-5): 386-94, 2004.
Artigo em Inglês | MEDLINE | ID: mdl-15764300

RESUMO

Little is known about the relevance of genetic polymorphisms to arsenic-related bladder cancer. A preliminary case-control study was conducted to explore the association between genetic polymorphisms of GSTT1, p53 codon 72 and bladder cancer in southern Taiwan, a former high arsenic exposure area. Fifty-nine urinary transitional cell carcinoma (TCC) patients from a referral centre in south-western Taiwan and 81 community controls matched on residence were recruited from 1996 to 1999. A questionnaire was administered to obtain arsenic exposure and general health information. Genotypes of p53 codon 72 and GSTT1 were analysed by polymerase chain reaction-restriction fragment length polymerase. The combined variant genotypes (heterozygous or homozygous variant) of p53 codon 72 and GSTT1 null were observed in 29% of cases and in 44% of controls, respectively. In this preliminary study, bladder cancer risk was slightly elevated for subjects carrying the variant genotype of p53 codon 72 or in subjects carrying the GSTT1 null genotype. Variants in p53 codon 72 increased the risk of bladder cancer among smokers. However, the results were not statistically significant and larger confirmatory studies are needed to clarify the role of candidate gene polymorphisms and bladder cancer risk in arsenic exposed populations.


Assuntos
Intoxicação por Arsênico/complicações , Carcinoma de Células de Transição/etiologia , Genes p53 , Glutationa Transferase/genética , Polimorfismo Genético , Neoplasias da Bexiga Urinária/etiologia , Adulto , Idoso , Carcinoma de Células de Transição/genética , Estudos de Casos e Controles , Códon , Feminino , Predisposição Genética para Doença , Humanos , Masculino , Pessoa de Meia-Idade , Fatores de Risco , Fumar , Taiwan , Neoplasias da Bexiga Urinária/genética
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