Medical Genomics Group, UCL Cancer Institute, University College London, 72 Huntley Street, London WC1E 6BT, UK.
Methods. 2010 Nov;52(3):248-54. doi: 10.1016/j.ymeth.2010.04.012. Epub 2010 Apr 29.
Aberrant DNA methylation of promoter and other genomic regions can lead to changes in gene expression, such as over-expression of oncogenes and the silencing of tumour suppressor genes in the context of cancer. Ability to accurately assess the DNA methylation status is therefore of great importance in health and disease. Recently, various platforms for genome-wide analysis of promoter DNA methylation have been developed, including the Illumina Infinium platform. While some of these platforms can be used with formalin-fixed paraffin-embedded (FFPE) tissue, no protocol has yet been developed for the analysis of FFPE-derived DNA on the Infinium platform using the HumanMethylation27 BeadChip which interrogates 27,578 cytosine-guanine (CpG) dinucleotide sites, selected predominantly from the promoter regions of 14,000 annotated genes. As FFPE preservation has been the method of choice for the archiving of clinical samples, the ability to analyse such samples opens the possibility to study large numbers of clinically well annotated samples which can be expected to lead to more powerful and robust data, particularly for rare cancers. Here, we describe a protocol for the analysis of FFPE samples using the Infinium HumanMethylation27 BeadChip.
启动子和其他基因组区域的异常 DNA 甲基化可导致基因表达的改变,例如在癌症情况下癌基因的过度表达和肿瘤抑制基因的沉默。因此,准确评估 DNA 甲基化状态在健康和疾病中非常重要。最近,已经开发出各种用于启动子 DNA 甲基化全基因组分析的平台,包括 Illumina Infinium 平台。虽然其中一些平台可用于福尔马林固定石蜡包埋(FFPE)组织,但尚未开发出用于在 Infinium 平台上分析 FFPE 衍生 DNA 的方案,该平台使用 HumanMethylation27 BeadChip 检测 27,578 个胞嘧啶-鸟嘌呤(CpG)二核苷酸位点,这些位点主要选自 14,000 个注释基因的启动子区域。由于 FFPE 保存一直是临床样本存档的首选方法,因此能够分析此类样本为研究大量临床注释良好的样本打开了可能性,这有望产生更强大和稳健的数据,特别是对于罕见癌症。在这里,我们描述了一种使用 Infinium HumanMethylation27 BeadChip 分析 FFPE 样本的方案。