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在一项大型癌症预防试验中,白细胞介素8及其受体基因的遗传变异及其对芬兰男性前列腺癌风险和预后的影响。

Genetic variation in interleukin 8 and its receptor genes and its influence on the risk and prognosis of prostate cancer among Finnish men in a large cancer prevention trial.

作者信息

Yang Hannah P, Woodson Karen, Taylor Philip R, Pietinen Pirjo, Albanes Demetrius, Virtamo Jarmo, Tangrea Joseph A

机构信息

Emerging Leaders Program, DHHS, Washington, DC, USA.

出版信息

Eur J Cancer Prev. 2006 Jun;15(3):249-53. doi: 10.1097/01.cej.0000199504.07947.e7.

Abstract

The cytokine interleukin 8 (IL-8) may play a role in the pathogenesis of prostate cancer through the modulation of tumour immune response or enhanced angiogenesis. A common polymorphism of the IL-8 (-251) gene, which may affect the production level of the cytokine, has been inversely associated with a number of diseases, including prostate cancer. We examined the most representative single nucleotide polymorphisms (SNPs) for the IL-8 and its receptors (CXCR1 and CXCR2) genes, and conducted a case-control study nested within the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study to examine if these SNPs are associated with susceptibility to and prognosis of prostate cancer. Using incidence density sampling, 584 cases of primary prostate cancer and 584 matched controls were selected. In this population, we observed no strong association between the SNPs for IL-8 -251 (A-->T), CXCR1 +860 (C-->G) and CXCR2 -1010 (A-->G) and either the subsequent risk of prostate cancer or individual prognostic factors among cases. Although none of the SNPs studied are likely to have major effects on prostate cancer susceptibility, a role for other polymorphisms associated within these genes cannot be excluded.

摘要

细胞因子白细胞介素8(IL-8)可能通过调节肿瘤免疫反应或增强血管生成在前列腺癌的发病机制中发挥作用。IL-8(-251)基因的一种常见多态性可能会影响该细胞因子的产生水平,它与包括前列腺癌在内的多种疾病呈负相关。我们检测了IL-8及其受体(CXCR1和CXCR2)基因最具代表性的单核苷酸多态性(SNP),并在α-生育酚、β-胡萝卜素癌症预防研究中开展了一项巢式病例对照研究,以检验这些SNP是否与前列腺癌的易感性和预后相关。采用发病密度抽样方法,选取了584例原发性前列腺癌病例和584例匹配对照。在该人群中,我们未观察到IL-8 -251(A→T)、CXCR1 +860(C→G)和CXCR2 -1010(A→G)的SNP与前列腺癌后续发病风险或病例中的个体预后因素之间存在强关联。虽然所研究的SNP均不太可能对前列腺癌易感性产生主要影响,但不能排除这些基因内其他相关多态性的作用。

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