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Provedor de dados:  BJMBR
País:  Brazil
Título:  CHRNA5 polymorphism and susceptibility to lung cancer in a Chinese population
Autores:  Shen,Bo
Zhu,Qun
Zheng,Ma-Qing
Chen,Jia
Shi,Mei-Qi
Feng,Ji-Feng
Data:  2013-01-01
Ano:  2013
Palavras-chave:  Lung cancer
Nicotinic acetylcholine receptors
CHRNA5 gene
Single nucleotide polymorphisms
Resumo:  Polymorphisms in the nicotinic acetylcholine receptor subunit CHRNA5 gene have been associated with lung cancer positive susceptibility in European and American populations. In the present hospital-based, case-control study, we determined whether polymorphism in rs503464 of CHRNA5 is associated with lung cancer risk in Chinese individuals. A single nucleotide polymorphism in CHRNA5 rs503464, c.-166T>A (hereafter T>A), was identified using TaqMan-MGB probes with sequencing via PCR in 600 lung cancer cases and 600 healthy individuals. Genotype frequencies for rs503464 (T>A) were in Hardy-Weinberg equilibrium for the control population. However, genotype frequencies were significantly different between cases and controls (P < 0.05), while allele frequencies were not significantly different between groups. Compared to homozygous genotypes (TT or AA), the risk of lung cancer in those with the heterozygous genotype (TA) was significantly lower (OR = 0.611, 95%CI = 0.486-0.768, P = 0.001). Using genotype AA as a reference, the risk of lung cancer for those with genotype TA was increased 1.5 times (OR = 1.496, 95%CI = 1.120-1.997, P = 0.006). However, no difference in risk was observed between T allele carriers and A allele carriers (OR = 0.914, 95%CI = 0.779-1.073, P = 0.270). Stratification analysis showed that the protective effect of TA was more pronounced in those younger than 60 years, nonsmokers, or those without a family history of cancer, as well as in patients with adenocarcinoma or squamous cell carcinoma in clinical stages III or IV (P < 0.05). Therefore, the heterozygous genotype c.-166T>A at rs503464 of CHRNA5 may be associated with reduced risk of lung cancer, thus representing a susceptibility allele in Chinese individuals.
Tipo:  Info:eu-repo/semantics/article
Idioma:  Inglês
Identificador:  http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2013000100079
Editor:  Associação Brasileira de Divulgação Científica
Relação:  10.1590/1414-431X20122451
Formato:  text/html
Fonte:  Brazilian Journal of Medical and Biological Research v.46 n.1 2013
Direitos:  info:eu-repo/semantics/openAccess
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