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ADH1B 和 ALDH2 多态性及其与韩国人群头颈部鳞状细胞癌风险增加的关联。

ADH1B and ALDH2 polymorphisms and their associations with increased risk of squamous cell carcinoma of the head and neck in the Korean population.

机构信息

Department of Otolaryngology-Head and Neck Surgery, College of Medicine, Hanyang University, Seongdong-Gu, Seoul, Republic of Korea.

出版信息

Oral Oncol. 2011 Jul;47(7):583-7. doi: 10.1016/j.oraloncology.2011.04.007. Epub 2011 May 14.

Abstract

Alcohol consumption is a major risk factor for squamous cell carcinoma of the head and neck (SCCHN). Alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) are key enzymes in ethanol metabolism. The objective of this study was to investigate the relationships of ADH and ALDH single nucleotide polymorphisms (SNPs) with the risk of developing SCCHN in a Korean sample. We genotyped ADH1B +3170A>G (rs1229984) and ALDH2 +1951G>A (rs671) SNPs in 225 Korean SCCHN patients and 301 healthy controls by single base extension and TaqMan assay. The frequencies of the ADH1B +3170A>G (22/21/11) genotypes were 48.0%/38.7%/13.3% in SCCHN patients, and 57.8%/37.2%/5.0% in controls, respectively. The odds ratio (OR) and 95% confidence interval of the ADH1B11 genotype was 1.89 (1.23-2.92) relative to the 22 genotype. The frequencies of the ALDH2 +1951G>A (11/12/22) genotypes were 67.6%/31.6%/0.9% in SCCHN patients, and 67.8%/29.6%/2.7% in controls, respectively. In subgroup analyses according to smoking and alcohol drinking status, the OR of the ADH1B11 genotype was increased in the heavy drinker group [8.85 (1.095-40.0)] and in the heavy smoker group [4.7 (1.54-14.29)]. We conclude that the ADH1B11 genotype is associated with an increased risk of SCCHN, especially in heavy drinkers and heavy smokers. This genotype could be a useful biomarker for identifying Koreans with a greater risk of SCCHN.

摘要

酒精摄入是头颈部鳞状细胞癌(SCCHN)的主要危险因素。乙醇代谢中的关键酶是醇脱氢酶(ADH)和醛脱氢酶(ALDH)。本研究旨在探讨韩国人群 ADH 和 ALDH 单核苷酸多态性(SNP)与 SCCHN 发病风险的关系。我们通过单碱基延伸和 TaqMan 检测法,对 225 例韩国 SCCHN 患者和 301 例健康对照者的 ADH1B+3170A>G(rs1229984)和 ALDH2+1951G>A(rs671)SNP 进行了基因分型。在 SCCHN 患者中,ADH1B+3170A>G(22/21/11)基因型的频率分别为 48.0%/38.7%/13.3%,而在对照组中,该频率分别为 57.8%/37.2%/5.0%。ADH1B11 基因型的比值比(OR)和 95%置信区间为 1.89(1.23-2.92),与22 基因型相比。在 SCCHN 患者中,ALDH2+1951G>A(11/12/22)基因型的频率分别为 67.6%/31.6%/0.9%,而在对照组中,该频率分别为 67.8%/29.6%/2.7%。根据吸烟和饮酒状况进行亚组分析,ADH1B11 基因型的 OR 在重度饮酒组[8.85(1.095-40.0)]和重度吸烟组[4.7(1.54-14.29)]中升高。我们的结论是,ADH1B11 基因型与 SCCHN 的发病风险增加相关,尤其是在重度饮酒者和重度吸烟者中。该基因型可能是识别韩国人群中 SCCHN 发病风险较高的有用生物标志物。

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