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GSTM1 缺失基因型是罗马尼亚散发性结直肠癌的危险因素。与 NAT2-快速乙酰化表型和环境因素暴露有关。

GSTM1-null genotype as a risk factor for sporadic colorectal cancer in a Romanian population. Association with the NAT2-rapid-acetylator phenotype and exposure to environmental factors.

机构信息

1Department of Medical Biochemistry, "Iuliu Hatieganu" University of Medicine and Pharmacy, Cluj-Napoca, Romania.

出版信息

Cancer Invest. 2014 Feb;32(2):53-62. doi: 10.3109/07357907.2013.867972.

Abstract

We evaluated the association between the presence of the GSTM1-null genotype and the combined presence of the GSTM1-null genotype/NAT2 rapid acetylator phenotype and the risk of developing sporadic colorectal cancer (CRC), as well as their interaction with environmental risk factors. One hundred and fifty patients with sporadic CRC and 162 controls were genotyped using PCR-RFLP analysis. For testing and quantification of the simple effect (main effect) and of the gene-gene and gene-environment interaction (modification effect), univariate and multivariate logistic regression was used. In the multiplicative model, from the genetic factors, GSTM1-null and NAT2*6B had a statistically significant influence on the risk for CRC, while from the environmental factors, smoking and diet had similar effects. The combination of GSTM1-null/NAT2 rapid acetylator phenotype/smoking behavior or GSTM1-null/NAT2 rapid acetylator phenotype/diet rich in fried red meat was not found to influence the sporadic CRC risk in Romanians, but the GSTM1-null genotype, NAT2 rapid acetylator phenotype influenced the sporadic CRC risk differently depending on the gender of the patient.

摘要

我们评估了 GSTM1 缺失基因型的存在以及 GSTM1 缺失基因型/ NAT2 快速乙酰化表型的共同存在与散发性结直肠癌(CRC)风险之间的关联,以及它们与环境危险因素的相互作用。使用 PCR-RFLP 分析对 150 例散发性 CRC 患者和 162 例对照进行基因分型。为了测试和量化简单效应(主效应)以及基因-基因和基因-环境相互作用(修饰效应),使用了单变量和多变量逻辑回归。在乘法模型中,从遗传因素来看,GSTM1 缺失和 NAT2*6B 对 CRC 风险有统计学意义的影响,而从环境因素来看,吸烟和饮食有类似的影响。在罗马尼亚人中,未发现 GSTM1 缺失/NAT2 快速乙酰化表型/吸烟行为或 GSTM1 缺失/NAT2 快速乙酰化表型/富含油炸红肉的饮食组合会影响散发性 CRC 风险,但 GSTM1 缺失基因型、NAT2 快速乙酰化表型会影响散发性 CRC 风险根据患者的性别而有所不同。

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