首页> 美国卫生研究院文献>Clinical Molecular Pathology >Genetic polymorphism of N-acetyltransferase-2 glutathione S-transferase-M1 and cytochromes P450IIE1 and P450IID6 in the susceptibility to head and neck cancer.
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Genetic polymorphism of N-acetyltransferase-2 glutathione S-transferase-M1 and cytochromes P450IIE1 and P450IID6 in the susceptibility to head and neck cancer.

机译:N-乙酰基转移酶-2谷胱甘肽S-转移酶-M1和细胞色素P450IIE1和P450IID6的遗传多态性对头颈癌的易感性。

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摘要

AIMS: To analyse the allele frequencies of DNA polymorphisms at the genes for cytochromes P450IIE1 and P450IID6, N-acetyltransferase-2, and glutathione S-transferase-M1 in patients with head and neck squamous cell carcinoma, in an attempt to define genetic factors involved in the susceptibility to this cancer, which is strongly associated with tobacco consumption. METHODS: Determination of restriction fragment length polymorphism (RFLP) at cytochromes P450IIE1/P450IID6 and NAT2 genes, and the presence of homozygous deletion of the GSTM1 gene, in 200 controls and 75 head and neck cancer patients. Allelic frequencies between the two groups were compared using a chi 2 test, and odds ratio with 95% confidence intervals were calculated. RESULTS: There was no evidence of an association between alleles of CYP2D6 and CYP2E1 and head and neck cancer in our population. Similarly, frequencies of individuals lacking the GSTM1 gene did not differ between controls and patients. However, individuals with the NAT2-SA phenotype were at higher risk of developing head and neck cancer. The frequencies of the most common SA genotype (homozygous for the NAT2*5 allele) were higher in patients than in controls (27% v 15%, respectively). Slow acetylators homozygous for the NAT2*6 allele, the second most common SA allele, were also more common in patients than in controls (11% v 5%, respectively). CONCLUSIONS: Slow NAT2 activity is a risk factor possibly leading to the development of head and neck cancer in response to tobacco carcinogens.
机译:目的:分析头颈部鳞状细胞癌患者细胞色素P450IIE1和P450IID6,N-乙酰基转移酶-2和谷胱甘肽S-转移酶-M1基因的DNA多态性等位基因频率,以试图确定涉及的遗传因素对这种癌症的易感性,这与烟草消费密切相关。方法:测定200例对照和75例头颈癌患者的细胞色素P450IIE1 / P450IID6和NAT2基因的限制性片段长度多态性(RFLP),以及GSTM1基因的纯合缺失。使用chi 2检验比较两组之间的等位基因频率,并计算95%置信区间的比值比。结果:没有证据表明CYP2D6和CYP2E1等位基因与我们人群的头颈癌相关。同样,对照组和患者之间缺乏GSTM1基因的个体频率也没有差异。但是,具有NAT2-SA表型的个体患头颈癌的风险较高。患者中最常见的SA基因型(NAT2 * 5等位基因为纯合子)的频率高于对照组(分别为27%和15%)。 NAT2 * 6等位基因(第二常见的SA等位基因)纯合子慢的乙酰化剂在患者中也比在对照组中更为常见(分别为11%和5%)。结论:缓慢的NAT2活性可能是导致对烟草致癌物的头颈癌发展的危险因素。

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