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Assessment of concordance between fresh-frozen and formalin-fixed paraffin embedded tumor DNA methylation using a targeted sequencing approach

机译:使用靶向测序方法评估新鲜冷冻和福尔马林固定石蜡包埋的肿瘤DNA甲基化之间的一致性

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摘要

DNA methylation is altered in many types of disease, including metastatic colorectal cancer. However, the methylome has not yet been fully described in archival formalin-fixed paraffin embedded (FFPE) samples in the context of matched fresh-frozen (FF) tumor material at base-pair resolution using a targeted approach. Using next-generation sequencing, we investigated three pairs of matched FFPE and FF samples to determine the extent of their similarity. We identified a ‘bowing’ pattern specific to FFPE samples categorized by a lower CG proportion at the start of sequence reads. We have found no evidence that this affected methylation calling, nor concordance of results. We also found no significant increase in deamination, measured by C>T transitions, previously considered a result of crosslinking DNA by formalin fixation and a barrier to the use of FFPE in methylation studies. The methods used in this study have shown sensitivity of between 60-70% based on positions also methylated in colorectal cancer cell lines. We demonstrate that FFPE material is a useful source of tumor material for methylation studies using targeted sequencing.
机译:DNA甲基化在许多类型的疾病(包括转移性结直肠癌)中发生改变。但是,在使用靶向方法以碱基对分辨率匹配的新鲜冷冻(FF)肿瘤材料的背景下,在归档福尔马林固定石蜡包埋(FFPE)样品中尚未完全描述甲基化组。使用下一代测序,我们研究了三对匹配的FFPE和FF样品,以确定它们的相似程度。在序列读取开始时,我们发现了特定于FFPE样品的“上升”模式,其中CG比例较低。我们没有发现证据表明这会影响甲基化反应,也没有结果的一致性。我们还没有发现脱氨作用的显着增加(通过C> T跃迁测量),以前认为这是通过福尔马林固定来交联DNA的结果,也是在甲基化研究中使用FFPE的障碍。基于在结肠直肠癌细胞系中也甲基化的位置,本研究中使用的方法显示出60-70%的敏感性。我们证明FFPE材料是使用靶向测序进行甲基化研究的有用肿瘤材料来源。

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