RNA Bioscience Initiative, and Department of Biochemistry and Molecular Genetics, University of Colorado School of Medicine, Mail Stop: 8101, 12801 East 17th Avenue L18-9102, Aurora, CO 80045, USA.
Open Biol. 2020 Sep;10(9):200119. doi: 10.1098/rsob.200119. Epub 2020 Sep 2.
Cell-free DNA (cfDNA) has the potential to enable non-invasive detection of disease states and progression. Beyond its sequence, cfDNA also represents the nucleosomal landscape of cell(s)-of-origin and captures the dynamics of the epigenome. In this review, we highlight the emergence of cfDNA epigenomic methods that assess disease beyond the scope of mutant tumour genotyping. Detection of tumour mutations is the gold standard for sequencing methods in clinical oncology. However, limitations inherent to mutation targeting in cfDNA, and the possibilities of uncovering molecular mechanisms underlying disease, have made epigenomics of cfDNA an exciting alternative. We discuss the epigenomic information revealed by cfDNA, and how epigenomic methods exploit cfDNA to detect and characterize cancer. Future applications of cfDNA epigenomic methods to act complementarily and orthogonally to current clinical practices has the potential to transform cancer management and improve cancer patient outcomes.
无细胞游离 DNA(cfDNA)具有实现疾病状态和进展的非侵入性检测的潜力。除了其序列外,cfDNA 还代表了起源细胞的核小体景观,并捕获了表观基因组的动态。在这篇综述中,我们强调了 cfDNA 表观基因组方法的出现,这些方法超越了突变肿瘤基因分型的范围来评估疾病。检测肿瘤突变是临床肿瘤学中测序方法的金标准。然而,cfDNA 中突变靶向固有的局限性,以及揭示疾病潜在分子机制的可能性,使得 cfDNA 的表观基因组学成为一个令人兴奋的替代方法。我们讨论了 cfDNA 揭示的表观基因组学信息,以及表观基因组学方法如何利用 cfDNA 来检测和表征癌症。cfDNA 表观基因组学方法未来的应用与当前临床实践互补和正交,有可能改变癌症管理并改善癌症患者的预后。