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首页> 外文期刊>International Journal of Cancer =: Journal International du Cancer >ANO7 is associated with aggressive prostate cancer
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ANO7 is associated with aggressive prostate cancer

机译:ANO7与侵略性前列腺癌有关

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Prostate cancer is one of the most common and heritable human cancers. Our aim was to find germline biomarkers that can predict disease outcome. We previously detected predisposing signals at 2q37, the location of the prostate specific ANO7 gene. To investigate, in detail, the associations between the ANO7 gene and PrCa risk and disease aggressiveness, ANO7 was sequenced in castration resistant tumors together with samples from unselected PrCa patients and unaffected males. Two pathogenic variants were discovered and genotyped in 1769 patients and 1711 unaffected males. Expression of ANO7 vs. PrCa aggressiveness was investigated. Different databases along with Swedish and Norwegian cohorts were used for validation. Case–control and aggressive vs. nonaggressive association analyses were performed against risk and/or cancer aggressiveness. The ANO7 mRNA level and patient survival were analyzed using expression data from databases. Variant rs77559646 showed both risk (OR 1.40; p = 0.009, 95% CI 1.09–1.78) and association with aggressive PrCa (Genotype test p = 0.04). It was found to be an eQTL for ANO7 (Linear model p ‐values for Finnish patients p = 0.009; Camcap prostate tumor p = 2.53E‐06; Stockholm prostate tumor cohort p = 1.53E‐13). rs148609049 was not associated with risk, but was related to shorter survival (HR 1.56; 95% CI 1.03–2.36). High ANO7 expression was independently linked to poor survival (HR 18.4; 95% CI 1.43–237). ANO7 genotypes correlate with expression and biochemical relapse, suggesting that ANO7 is a potential PrCa susceptibility gene and that its elevated expression correlates with disease severity and outcome.
机译:前列腺癌是最常见和最常见的人类癌症之一。我们的目标是找到可以预测疾病结果的种系生物标志物。之前,我们以前检测到2Q37的预测信号,前列腺特异性ANO7基因的位置。为了详细研究Ano7基因和PRCA风险和疾病侵袭性的关联,ANO7在阉割的抗肿瘤中测序,与未选择的PRCA患者和未受影响的雄性的样品一起测序。在1769名患者中发现并基因分型发现了两种致病变异,1711年不受影响的雄性。调查了ANO7与PRCA侵略性的表达。使用不同的数据库以及瑞典和挪威队列的验证。案例控制和侵略性与非收入关联分析进行风险和/或癌症侵略性进行。使用来自数据库的表达数据分析ANO7 mRNA水平和患者存活。变型RS77559646显示风险(或1.40; p = 0.009,95%CI 1.09-1.78)和侵略性PRCA的关联(基因型检验P = 0.04)。发现它是ANO7的EQTL(用于芬兰患者的线性模型P-Values p = 0.009; Camcap前列腺肿瘤P = 2.53E-06;斯德哥尔摩前列腺肿瘤队队列P = 1.53E-13)。 RS148609049与风险无关,但与较短的存活相关(HR 1.56; 95%CI 1.03-2.36)。高ANO7表达与存活率差(HR 18.4; 95%CI 1.43-237)独立相关联。 ANO7基因型与表达和生化复发相关,表明ANO7是潜在的PRCA易感基因,其表达升高与疾病严重程度和结果相关。

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