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Diagnosis and Prognostication of Ductal Adenocarcinomas of the Pancreas Based on Genome-Wide DNA Methylation Profiling by Bacterial Artificial Chromosome Array-Based Methylated CpG Island Amplification

机译:基于细菌人工染色体阵列的甲基化CpG岛扩增的全基因组DNA甲基化谱分析的胰腺导管腺癌的诊断和预后。

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摘要

To establish diagnostic criteria for ductal adenocarcinomas of the pancreas (PCs), bacterial artificial chromosome (BAC) array-based methylated CpG island amplification was performed using 139 tissue samples. Twelve BAC clones, for which DNA methylation status was able to discriminate cancerous tissue (T) from noncancerous pancreatic tissue in the learning cohort with a specificity of 100%, were identified. Using criteria that combined the 12 BAC clones, T-samples were diagnosed as cancers with 100% sensitivity and specificity in both the learning and validation cohorts. DNA methylation status on 11 of the BAC clones, which was able to discriminate patients showing early relapse from those with no relapse in the learning cohort with 100% specificity, was correlated with the recurrence-free and overall survival rates in the validation cohort and was an independent prognostic factor by multivariate analysis. Genome-wide DNA methylation profiling may provide optimal diagnostic markers and prognostic indicators for patients with PCs.
机译:为了建立胰腺导管腺癌(PCs)的诊断标准,使用139个组织样本进行了基于细菌人工染色体(BAC)阵列的甲基化CpG岛扩增。鉴定了十二个BAC克隆,它们的DNA甲基化状态能够区分学习人群中癌组织(T)与非癌胰腺组织,特异性为100%。使用结合了12个BAC克隆的标准,在学习和验证队列中,T样本被诊断为具有100%敏感性和特异性的癌症。 BAC克隆中的11个DNA甲基化状态能够以100%的特异性区分学习队列中无复发的患者和无复发的患者,与验证队列中的无复发率和总生存率相关,并且通过多变量分析得出独立的预后因素。全基因组DNA甲基化分析可能为PC病患提供最佳的诊断标记和预后指标。

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