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Extraction and Processing of Circulating DNA from Large Sample Volumes using Methylation on Beads for the Detection of Rare Epigenetic Events

机译:使用甲基化对珠子进行罕见的表观遗传事件检测从大体积样品中提取和处理循环DNA

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摘要

The use of methylated tumor-specific circulating DNA has shown great promise as a potential cancer biomarker. Nonetheless, the relative scarcity of tumor-specific circulating DNA presents a challenge for traditional DNA extraction and processing techniques. Here we demonstrate a single tube extraction and processing technique dubbed “methylation on beads” that allows for DNA extraction and bisulfite conversion for up to 2 ml of plasma or serum. In comparison to traditional techniques including phenol chloroform and alcohol extraction, methylation on beads yields a 1.5 to 5-fold improvement in extraction efficiency. The technique results in far less carryover of PCR inhibitors yielding analytical sensitivity improvements of over 25-fold. The combination of improved recovery and sensitivity make possible the detection of rare epigenetic events and the development of high sensitivity epigenetic diagnostic assays.
机译:甲基化肿瘤特异性循环DNA的使用已显示出作为潜在的癌症生物标志物的巨大希望。然而,肿瘤特异性循环DNA的相对稀缺性对传统的DNA提取和加工技术提出了挑战。在这里,我们展示了一种称为“珠上甲基化”的单管提取和加工技术,该技术可用于最多2 ml血浆或血清的DNA提取和亚硫酸氢盐转化。与包括苯酚氯仿和乙醇提取的传统技术相比,在珠上进行甲基化可使提取效率提高1.5至5倍。该技术可大大减少PCR抑制剂的残留,从而使分析灵敏度提高25倍以上。提高的回收率和灵敏度的结合使检测罕见的表观遗传事件和开发高灵敏度的表观遗传诊断方法成为可能。

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