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胰岛素样生长因子结合蛋白 3(IGFBP3)基因中单核苷酸多态性(rs2854744)与膀胱癌风险的关系。

Urinary bladder cancer risk in relation to a single nucleotide polymorphism (rs2854744) in the insulin-like growth factor-binding protein-3 (IGFBP3) gene.

机构信息

Leibniz Research Centre for Working Environment and Human Factors (IfADo), Ardeystrasse 67, 44139, Dortmund, Germany.

出版信息

Arch Toxicol. 2012 Feb;86(2):195-203. doi: 10.1007/s00204-011-0747-5. Epub 2011 Sep 3.

Abstract

Currently, twelve validated genetic variants have been identified that are associated with urinary bladder cancer (UBC) risk. However, those validated variants explain only 5-10% of the overall inherited risk. In addition, there are more than 100 published polymorphisms still awaiting validation or disproval. A particularly promising of the latter unconfirmed polymorphisms is rs2854744 that recently has been published to be associated with UBC risk. The [A] allele of rs2854744 has been reported to be associated with a higher promoter activity of the insulin-like growth factor-binding protein-3 (IGFBP3) gene, which may lead to increased IGFBP-3 plasma levels and cancer risk. Therefore, we investigated the association of rs2854744 with UBC in the IfADo case-control series consisting of 1,450 cases and 1,725 controls from Germany, Hungary, Venezuela and Pakistan. No significant association of rs2854744 with UBC risk was obtained (all study groups combined: unadjusted P = 0.4446; adjusted for age, gender and smoking habits P = 0.6510), besides a small effect of the [A] allele in the Pakistani study group opposed to the original findings (unadjusted P = 0.0508, odds ratio (OR) = 1.43 for the multiplicative model) that diminished after adjustment for age, gender and smoking habits (P = 0.7871; OR = 0.93). Associations of rs2854744 with occupational exposure to urinary bladder carcinogens and smoking habits were also not present. A meta-analysis of all available case-control series including the original discovery study resulted in an OR of 1.00 (P = 0.9562). In conclusion, we could not confirm the recently published hypothesis that rs2854744 in the IGFBP3 gene is associated with UBC risk.

摘要

目前,已经确定了 12 个与膀胱癌 (UBC) 风险相关的经过验证的遗传变异。然而,这些经过验证的变异仅解释了整体遗传风险的 5-10%。此外,还有 100 多个已发表的多态性仍在等待验证或反驳。后者未确认的多态性中一个特别有前途的是 rs2854744,最近有研究表明它与 UBC 风险相关。rs2854744 的 [A] 等位基因已被报道与胰岛素样生长因子结合蛋白 3 (IGFBP3) 基因的启动子活性更高相关,这可能导致 IGFBP-3 血浆水平升高和癌症风险增加。因此,我们在由德国、匈牙利、委内瑞拉和巴基斯坦的 1450 例病例和 1725 例对照组成的 IfADo 病例对照系列中研究了 rs2854744 与 UBC 的关系。没有发现 rs2854744 与 UBC 风险之间存在显著关联(所有研究组合并:未调整的 P = 0.4446;调整年龄、性别和吸烟习惯后的 P = 0.6510),除了巴基斯坦研究组中 [A] 等位基因的小效应与原始发现相反(未调整的 P = 0.0508,乘法模型的优势比 (OR) = 1.43),该效应在调整年龄、性别和吸烟习惯后减弱(P = 0.7871;OR = 0.93)。rs2854744 与职业性接触膀胱癌致癌物和吸烟习惯之间也没有关联。对所有可用病例对照系列(包括原始发现研究)进行的荟萃分析得出的 OR 为 1.00(P = 0.9562)。总之,我们不能证实最近发表的假设,即 IGFBP3 基因中的 rs2854744 与 UBC 风险相关。

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