期刊
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE
卷 7, 期 3, 页码 307-312出版社
WILEY
DOI: 10.1111/j.1582-4934.2003.tb00231.x
关键词
carcinoma; squamous cell; laryngeal neoplasms; gene deletion; GSTM1; alleles; gene frequency
This paper aimed to analyze the association of polymorphism of GSTM1 0/0 genotype with laryngeal cancer along a hospital based case-control study. Polymorphisms of GSTM 1 0/0 of samples from 36 patients with laryngeal cancer and 3 5 healthy controls were detected by PCR method. The reaction used as GSTM I primers, using the sequence sense: 5'-CTGCCCTACTTGGATTGATGGG-3' and antisense: 5'-TGGATTGTAGCAGATCATGC-3'. N Acetyl transferase I (NAT1) gene using the primers sense: 5'-TAAAAGTAAAATGATTTGCTTTCG-3' and antisense: 5'-GCTTTCTAGCATAAATCACCAA-3' was used as internal positive control. Two sided 2 and multivariation analysis were used to analyse the results. The proportions of GSTM I deleted genotype in cases and controls were 47.2% and 54.3%, respectively. There was significant increment of GSTM 0/0 genotype frequency in moderate smokers group of patients compared to control (P=0.033, OR=4.78, 95% Cl=1.30-7.13). We conclude that GSTM1 deleted genotype may be a genetic susceptibility marker for laryngeal cancer whose exposed to low doses carcinogens. The absence of this enzyme seems to have a role in the development of laryngeal cancer, in which the mechanism still needs further investigation.
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