Departments of Bioengineering and Applied Physics, Stanford University, Stanford, CA 94305, USA.
Current address: Ludwig Institute for Cancer Research and Target Discovery Institute, Nuffield Department of Medicine, University of Oxford, Oxford OX3 7FZ, UK.
Cell Res. 2017 Oct;27(10):1231-1242. doi: 10.1038/cr.2017.106. Epub 2017 Aug 18.
5-Hydroxymethylcytosine (5hmC) is an important mammalian DNA epigenetic modification that has been linked to gene regulation and cancer pathogenesis. Here we explored the diagnostic potential of 5hmC in circulating cell-free DNA (cfDNA) using a sensitive chemical labeling-based low-input shotgun sequencing approach. We sequenced cell-free 5hmC from 49 patients of seven different cancer types and found distinct features that could be used to predict cancer types and stages with high accuracy. Specifically, we discovered that lung cancer leads to a progressive global loss of 5hmC in cfDNA, whereas hepatocellular carcinoma and pancreatic cancer lead to disease-specific changes in the cell-free hydroxymethylome. Our proof-of-principle results suggest that cell-free 5hmC signatures may potentially be used not only to identify cancer types but also to track tumor stage in some cancers.
5-羟甲基胞嘧啶(5hmC)是一种重要的哺乳动物 DNA 表观遗传修饰,与基因调控和癌症发病机制有关。在这里,我们使用灵敏的基于化学标记的低输入鸟枪法测序方法探索了循环游离 DNA(cfDNA)中 5hmC 的诊断潜力。我们对来自 7 种不同癌症类型的 49 名患者的游离 5hmC 进行了测序,发现了可以用于高精度预测癌症类型和阶段的独特特征。具体而言,我们发现肺癌导致 cfDNA 中 5hmC 的全局逐渐丢失,而肝细胞癌和胰腺癌导致游离羟甲基组的疾病特异性变化。我们的原理验证结果表明,游离 5hmC 特征不仅可能用于识别癌症类型,而且可能用于跟踪某些癌症的肿瘤分期。