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Identification of specific DNA methylation sites on the Y-chromosome as biomarker in prostate cancer

机译:鉴定Y染色体上特定的DNA甲基化位点作为前列腺癌的生物标志物

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摘要

As a diagnostic biomarker, prostate special antigen (PSA) tests always generate false positive results and lead to unnecessary and/or repeat biopsies. Therefore, there is an urgent need for developing more sensitive, specific diagnostic biomarkers. We epigenotyped methylated sites in cancer tissues and adjacent normal tissues from 66 patients. In comparation with normal adjacent tissues, we observed that there were 6 aberrant methylation sites in prostate cancer tissues on the Y-chromosome. We further performed pyrosequencing using urine of PCa patients and we identified one methylated site (cg05163709) as a potential biomarker. We evaluated the predictive capacity of the aberrant methylated sites using the area under receiver operating characteristic (ROC) curve (AUC). The ROC analysis showed a higher AUC for cg05163709 (0.915) than prostate-specific antigen (PSA, 0.769). These results indicated that aberrant DNA methylation of cg05163709 on the Y-chromosome could serve as a potential diagnostic biomarker with high sensitivity and specificity.
机译:作为诊断性生物标志物,前列腺特殊抗原(PSA)测试始终会产生假阳性结果,并导致不必要的和/或重复的活检。因此,迫切需要开发更敏感的,特异性的诊断生物标志物。我们对66名患者的癌组织和邻近正常组织中的甲基化位点进行了表型分型。与正常的相邻组织相比,我们观察到Y染色体上前列腺癌组织中有6个异常甲基化位点。我们进一步使用PCa患者的尿液进行焦磷酸测序,我们确定了一个甲基化位点(cg05163709)作为潜在的生物标记物。我们使用接收器工作特征(ROC)曲线(AUC)下的面积评估了异常甲基化位点的预测能力。 ROC分析显示cg05163709(0.915)的AUC高于前列腺特异性抗原(PSA,0.769)。这些结果表明Y染色体上cg05163709的异常DNA甲基化可以作为具有高灵敏度和特异性的潜在诊断生物标志物。

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