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白细胞介素-1β基因多态性、吸烟和饮酒对非小细胞肺癌风险的影响。

Influence of interleukin-1 beta genetic polymorphism, smoking and alcohol drinking on the risk of non-small cell lung cancer.

机构信息

Department of Respiratory, Zhongnan Hospital, Wuhan University, Donghu Road 169 Wuhan 430071, PR China.

出版信息

Clin Chim Acta. 2010 Oct 9;411(19-20):1441-6. doi: 10.1016/j.cca.2010.05.035. Epub 2010 Jun 4.

DOI:10.1016/j.cca.2010.05.035
PMID:20529668
Abstract

BACKGROUND

Non-small cell cancer (NSCLC) accounts for approximately 80% of all lung cancers. Reports suggested an association between the interleukin-1beta (IL-1beta) -31 and -511 gene loci and NSCLC, but few studies took into account the effect of smoking and/or alcohol drinking on the association.

METHODS

Two-hundred thirteen cases of NSCLC (aged 58.2 + or - 10.1) and 213 controls (aged 59.4 + or - 10.3y) were included in this research. Information about the smoking and drinking behaviors, dietary customs, and anamnesis were obtained from all subjects by questionnaires, and genomic DNA was extracted. IL-1beta -31 and -511 gene polymorphisms were detected using PCR-RFLP. The interactions between the genotypes and alcohol drinking/smoking were analyzed using multivariate logistic regression models.

RESULTS

(The T/T genotype and the T allele of the IL-1beta -31 gene were associated with higher incidence of NSCLC (P<0.05). For the IL-1beta -511 locus, no difference was found in different genotypes between the NSCLC and control groups. After the adjustment of confounding variables, such as age and gender, the binary logistic analysis showed a significant gene-environment interaction (P<0.05).

CONCLUSIONS

The IL-1beta -31T allele was positively associated with a risk of NSCLC, and the carriers of IL-1beta -31T/T or -511C/C would have a higher risk of suffering from NSCLC if they drank alcohol or smoke heavily.

摘要

背景

非小细胞肺癌(NSCLC)约占所有肺癌的 80%。有报道称白细胞介素-1β(IL-1β)-31 和-511 基因座与 NSCLC 之间存在关联,但很少有研究考虑吸烟和/或饮酒对这种关联的影响。

方法

本研究纳入了 213 例 NSCLC 病例(年龄 58.2±10.1)和 213 例对照(年龄 59.4±10.3 岁)。通过问卷从所有受试者中获得吸烟和饮酒行为、饮食习惯和病史等信息,并提取基因组 DNA。采用 PCR-RFLP 法检测 IL-1β-31 和-511 基因多态性。采用多变量 logistic 回归模型分析基因型与饮酒/吸烟之间的相互作用。

结果

(IL-1β-31 基因的 T/T 基因型和 T 等位基因与 NSCLC 的发生呈正相关(P<0.05)。对于 IL-1β-511 基因座,在 NSCLC 组和对照组之间,不同基因型之间没有差异。在调整年龄和性别等混杂变量后,二元逻辑分析显示存在显著的基因-环境相互作用(P<0.05)。

结论

IL-1β-31T 等位基因与 NSCLC 的发病风险呈正相关,如果携带 IL-1β-31T/T 或-511C/C 基因型的个体大量饮酒或吸烟,患 NSCLC 的风险会更高。

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