首页> 外文期刊>Breast Cancer Research and Treatment >The Leu33Pro polymorphism in the ITGB3 gene does not modify BRCA1/2-associated breast or ovarian cancer risks: results from a multicenter study among 15,542 BRCA1 and BRCA2 mutation carriers
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The Leu33Pro polymorphism in the ITGB3 gene does not modify BRCA1/2-associated breast or ovarian cancer risks: results from a multicenter study among 15,542 BRCA1 and BRCA2 mutation carriers

机译:ITGB3基因中的Leu33Pro多态性不会改变BRCA1 / 2相关的乳腺癌或卵巢癌风险:来自15,542个BRCA1和BRCA2突变携带者的多中心研究结果

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摘要

Integrins containing the β3 subunit are key players in tumor growth and metastasis. A functional Leu33Pro polymorphism (rs5918) in the β3 subunit of the integrin gene (ITGB3) has previously been suggested to act as a modifier of ovarian cancer risk in Polish BRCA1 mutation carriers. To investigate the association further, we genotyped 9,998 BRCA1 and 5,544 BRCA2 mutation carriers from 34 studies from the Consortium of Investigators of Modifiers of BRCA1/2 for the ITGB3 Leu33Pro polymorphism. Data were analysed within a Cox-proportional hazards framework using a retrospective likelihood approach. There was marginal evidence that the ITGB3 polymorphism was associated with an increased risk of ovarian cancer for BRCA1 mutation carriers (per-allele Hazard Ratio (HR) 1.11, 95% CI 1.00–1.23, p-trend 0.05). However, when the original Polish study was excluded from the analysis, the polymorphism was no longer significantly associated with ovarian cancer risk (HR 1.07, 95% CI 0.96–1.19, p-trend 0.25). There was no evidence of an association with ovarian cancer risk for BRCA2 mutation carriers (HR 1.09, 95% CI 0.89–1.32). The polymorphism was not associated with breast cancer risk for either BRCA1 or BRCA2 mutation carriers. The ITGB3 Leu33Pro polymorphism does not modify breast or ovarian cancer risk in BRCA1 or BRCA2 mutation carriers.
机译:含有β 3 亚基的整合素是肿瘤生长和转移的关键因素。先前已提出整合蛋白基因(ITGB3)的β 3 亚基中的功能性Leu33Pro多态性(rs5918)可作为波兰BRCA1突变携带者中卵巢癌风险的调节剂。为了进一步研究该关联,我们对来自ITCA3 Leu33Pro多态性的BRCA1 / 2修饰子研究者协会的34个研究的9,998个BRCA1和5,544个BRCA2突变携带者进行了基因分型。使用回顾性似然方法在Cox比例风险框架内分析数据。有少量证据表明,ITGB3基因多态性与BRCA1突变携带者患卵巢癌的风险增加相关(每等位基因危险比(HR)1.11,95%CI 1.00-1.23,p-趋势0.05)。但是,当将最初的波兰研究排除在分析范围之外时,多态性不再与卵巢癌风险显着相关(HR 1.07,95%CI 0.96-1.19,p-趋势0.25)。没有证据表明BRCA2突变携带者与卵巢癌风险相关(HR 1.09,95%CI 0.89–1.32)。多态性与BRCA1或BRCA2突变携带者的乳腺癌风险无关。 ITGB3 Leu33Pro多态性不会改变BRCA1或BRCA2突变携带者中乳腺癌或卵巢癌的风险。

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