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Using gene expression from urine sediment to diagnose prostate cancer: development of a new multiplex mRNA urine test and validation of current biomarkers

机译:利用尿沉渣中的基因表达来诊断前列腺癌:开发一种新型的多重mRNA尿液测试和当前生物标志物的验证

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Background Additional accurate non-invasive biomarkers are needed in the clinical setting to improve prostate cancer (PCa) diagnosis. Here we have developed a new and improved multiplex mRNA urine test to detect prostate cancer (PCa). Furthermore, we have validated the PCA3 urinary transcript and some panels of urinary transcripts previously reported as useful diagnostic biomarkers for PCa in our cohort. Methods Post-prostatic massage urine samples were prospectively collected from PCa patients and controls. Expression levels of 42 target genes selected from our previous studies and from the literature were studied in 224 post-prostatic massage urine sediments by quantitative PCR. Univariate logistic regression was used to identify individual PCa predictors. A variable selection method was used to develop a multiplex biomarker model. Discrimination was measured by ROC curve AUC for both, our model and the previously published biomarkers. Results Seven of the 42 genes evaluated ( PCA3, ELF3, HIST1H2BG, MYO6, GALNT3, PHF12 and GDF15 ) were found to be independent predictors for discriminating patients with PCa from controls. We developed a four-gene expression signature ( HIST1H2BG, SPP1, ELF3 and PCA3 ) with a sensitivity of 77?% and a specificity of 67?% (AUC?=?0.763) for discriminating between tumor and control urines. The accuracy of PCA3 and previously reported panels of biomarkers is roughly maintained in our cohort. Conclusions Our four-gene expression signature outperforms PCA3 as well as previously reported panels of biomarkers to predict PCa risk. This study suggests that a urinary biomarker panel could improve PCa detection. However, the accuracy of the panels of urinary transcripts developed to date, including our signature, is not high enough to warrant using them routinely in a clinical setting.
机译:背景技术在临床环境中需要其他准确的非侵入性生物标记物以改善前列腺癌(PCa)的诊断。在这里,我们开发了一种新的且经过改进的多重mRNA尿液检测,以检测前列腺癌(PCa)。此外,我们已经验证了PCA3尿成绩单和先前报道的一些泌尿成绩单组在我们的队列中对PCa有用的诊断生物标记物。方法前瞻性地从PCa患者和对照组中收集按摩后尿液样本。通过定量PCR研究了从我们先前的研究和文献中选择的42个靶基因的表达水平,对224种前列腺按摩后尿液沉积物进行了研究。单变量逻辑回归用于确定个体PCa预测因子。使用变量选择方法来建立多重生物标志物模型。通过ROC曲线AUC对我们的模型和先前发布的生物标志物进行区分。结果发现评估的42个基因中有7个(PCA3,ELF3,HIST1H2BG,MYO6,GALNT3,PHF12和GDF15)是将PCa患者与对照区分开的独立预测因子。我们开发了一种四基因表达标记(HIST1H2BG,SPP1,ELF3和PCA3),可区分肿瘤和对照尿,敏感性为77%,特异性为67%(AUCα=α0.763)。 PCA3和先前报道的生物标志物组的准确性在我们的研究组中大致得以维持。结论我们的四基因表达签名优于PCA3以及先前报道的可预测PCa风险的生物标志物。这项研究表明,尿液生物标志物检测组可以改善PCa检测。但是,迄今为止,包括我们的签名在内的泌尿成绩单的准确性均不足以保证在临床环境中常规使用它们。

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