首页> 外文期刊>Neoplasma: Journal of Experimental and Clinical Oncology >Genetic polymorphism at GSTM1 and GSTT1 gene loci and susceptibility to oral cancer.
【24h】

Genetic polymorphism at GSTM1 and GSTT1 gene loci and susceptibility to oral cancer.

机译:GSTM1和GSTT1基因位点的遗传多态性和对口腔癌的易感性。

获取原文
获取原文并翻译 | 示例
           

摘要

GSTs are phase II enzymes which are involved in the detoxification of active metabolites of many potential carcinogens from tobacco smoke and therefore may play an important role in modulating susceptibility to tobacco related cancers. This study evaluates the influence of genetic polymorphisms of GSTM1 and GSTT1 gene loci on susceptibility to oral cancer. The genotyping was based on multiplex PCR assay that identified the GSTM1 and GSTT1 null (-/-) genotypes but didn't distinguish homozygous wild type+/+ and heterozygous +/- individuals. Genomic DNA was isolated from cases with oral cancer (n=40) and normal controls (n=87). The prevalence of the GSTM1 null genotypes was 29/87 (33.3%) and 21/40 (52.5%) in controls and oral cancer cases, respectively but the differences were not significant (OR=2.2; 95%CI=0.96-5.1; p=0.06). The frequency of homozygous GSTT1 null genotype in cancer cases was 17/40 (42.5%) as compared to 13/87 (14.94%) in controls and the differences were highly significant (OR=4.2; 95%CI=1.64-10.9; p=0.0002). Oral cancer cases had higher proportion of both GSTM1 and GSTT1 null genotypes as compared to controls but the differences were not statistically significant (OR=2.9; 95%CI=0.71-11.9; p=0.17). When individuals were categorized into two groups, no differences were observed for GSTM1 null genotype frequencies in control and cancer cases (OR=2.9; 95%CI=0.9-9.6; p=0.08) (OR=1.6; 95%CI=0.44-6.1; p=0.58) in <=50 yrs and >50 yrs of age groups. Significant differences between control and cancer cases were observed for GSTT1 null genotypes both in <=50 yrs and >50yrs of age groups (OR=4.0; 95%CI=1.1-15.0; p=0.03) (OR=4.5; 95%CI=0.97-22.29; p=0.05), respectively. The effect of smoking on GSTM1 null individuals was not found significant (OR=1.0; 95%CI=0.19-4.86; p=0.75) but it was significant in case of GSTT1 null individuals (OR=6.33; 95%CI=1.0-44.1; p=0.02). Our results thus suggest that GSTT1 gene polymorphisms modulate susceptibility to tobacco-related cancer of the oral cavity.
机译:GST是II期酶,参与烟草烟雾中许多潜在致癌物的活性代谢产物的解毒,因此可能在调节对烟草相关癌症的敏感性中起重要作用。本研究评估了GSTM1和GSTT1基因位点的遗传多态性对口腔癌易感性的影响。基因分型基于多重PCR检测,该检测确定了GSTM1和GSTT1无效(-/-)基因型,但没有区分纯合野生型+ / +和杂合+/-个体。从患有口腔癌(n = 40)和正常对照(n = 87)的病例中分离基因组DNA。在对照组和口腔癌病例中,GSTM1无效基因型的患病率分别为29/87(33.3%)和21/40(52.5%),但差异不显着(OR = 2.2; 95%CI = 0.96-5.1; OR = 2.2)。 p = 0.06)。与对照组的13/87(14.94%)相比,癌症病例中纯合GSTT1无效基因型的频率为17/40(42.5%),差异非常显着(OR = 4.2; 95%CI = 1.64-10.9; p = 0.0002)。与对照组相比,口腔癌病例的GSTM1和GSTT1无效基因型比例更高,但差异无统计学意义(OR = 2.9; 95%CI = 0.71-11.9; p = 0.17)。当将个体分为两组时,在对照和癌症病例中,GSTM1无效基因型频率没有观察到差异(OR = 2.9; 95%CI = 0.9-9.6; p = 0.08)(OR = 1.6; 95%CI = 0.44- 6.1; p = 0.58)在<= 50岁和> 50岁的年龄组中。在<= 50岁和> 50岁年龄段(OR = 4.0; 95%CI = 1.1-15.0; p = 0.03)的年龄组中,GSTT1无效基因型的对照和癌症病例之间存在显着差异(OR = 4.5; 95%CI = 0.97-22.29; p = 0.05)。吸烟对GSTM1无效个体的影响未发现显着(OR = 1.0; 95%CI = 0.19-4.86; p = 0.75),但对GSTT1无效个体的影响显着(OR = 6.33; 95%CI = 1.0- 44.1; p = 0.02)。因此,我们的结果表明GSTT1基因多态性可调节对口腔烟草相关癌症的敏感性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号