Scientific Reports · 2020 · 15 citations · 30 references
MedicineGeneticsMolecular BiologyAgingEpigeneticsGenomicsCellular AgingDna MethylationDna Methylation ProfilingEpigenetic Biomarker AnalysisEpigenetic BiomarkersEpigenetics Of AgingAge-associated Dna Methylation ChangesAge-related Methylation MarkersAging-associated Epigenetic ChangesCell-free Dna Methylation AnalysisCell-type Specific MethylationDna Methylation PatternsEpigenetic Aging MarkersRetrotransposition
LINE-1 hypomethylation of cell-free DNA has been described as an epigenetic biomarker of human aging. However, in the past, insufficient differentiation between cellular and cell-free DNA may have confounded analyses of genome-wide methylation levels in aging cells. Here we present a new methodological strategy to properly and unambiguously extract DNA methylation patterns of repetitive, as well as single genetic loci from pure cell-free DNA from peripheral blood. Since this nucleic acid fraction originates mainly in apoptotic, senescent and cancerous cells, this approach allows efficient analysis of aged and cancerous cell-specific DNA methylation patterns for diagnostic and prognostic purposes. Using this methodology, we observe a significant age-associated erosion of LINE-1 methylation in cfDNA suggesting that the threshold of hypomethylation sufficient for relevant LINE-1 activation and consequential harmful retrotransposition might be reached at higher age. We speculate that this process might contribute to making aging the main risk factor for many cancers.
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