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Biomarkers ; 17(1): 9-15, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22080860

RESUMO

OBJECTIVE: To explore the association between polymorphism of the human leukocyte antigen G (HLA-G) and susceptibility of esophageal carcinoma (EC) in Kazakh and Han nationality in Xinjiang. METHODS: The 14 bp deletion/insertion (rs16375) and 0105N (rs41557518) of HLA-G genotyping were determined by PCR and PCR-RFLP, respectively in 239 patients and 467 controls. RESULTS: There was a 2.69-fold (P(c) = 0.04, 95% CI: 1.30-5.55) increased risk of developing EC in individuals with the -14 bp/-14 bp genotype (rs16375) compared with those carrying +14 bp/+14 bp genotype in Kazakh after Bonferroni correction, there was no association of 0105N (rs41557518) both in Kazak and Han population. And there was a 2.82-fold (P(c) = 0.04, 95% CI: 1.32-6.04) increased risk of developing EC in individuals with -14 bp/-14 bp and C/C genotypes compared with those who had +14 bp/+14 bp and C/C genotypes in Kazakh. CONCLUSIONS: The study demonstrates that EC is associated with polymorphism of HLA-G14 bp in Chinese Kazak population. The 14 bp deletion/insertion of HLA-G gene may play a role in EC susceptibility of Kazakh.


Assuntos
Neoplasias Esofágicas/genética , Predisposição Genética para Doença/genética , Antígenos HLA-G/genética , Polimorfismo de Fragmento de Restrição/genética , Idoso , Povo Asiático/genética , Estudos de Casos e Controles , China/etnologia , Neoplasias Esofágicas/etnologia , Etnicidade/genética , Feminino , Predisposição Genética para Doença/etnologia , Humanos , Masculino , Pessoa de Meia-Idade , Mutagênese Insercional , Deleção de Sequência
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