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Unveiling targeted cell-free DNA methylation regions through paired methylome analysis of tumor and normal tissues. | LitMetric

AI Article Synopsis

  • Liquid biopsy analysis of cell-free DNA (cfDNA) has transformed cancer research by allowing non-invasive evaluation of genetic changes in tumors, especially for head and neck squamous cell carcinoma (HNSC).
  • This study utilized paired-sample differential methylation analysis to identify overlapping hypermethylated regions across two major datasets, reinforcing the potential of these regions as cfDNA biomarkers.
  • Several candidate genes were identified that have previously been linked to liquid biopsy in various cancers, and the study demonstrates the effectiveness of the psDMR analysis for discovering cfDNA methylation biomarkers, aiding in early cancer detection and monitoring.

Article Abstract

Liquid biopsy analysis of cell-free DNA (cfDNA) has revolutionized cancer research by enabling non-invasive assessment of tumor-derived genetic and epigenetic changes. In this study, we conducted a comprehensive paired-sample differential methylation analysis (psDMR) on reprocessed methylation data from two large datasets, CPTAC and TCGA, to identify and validate differentially methylated regions (DMRs) as potential cfDNA biomarkers for head and neck squamous cell carcinoma (HNSC). Our hypothesis is that the paired sample test provides a more suitable and powerful approach for the analysis of heterogeneous cancers like HNSC. The psDMR analysis revealed a significant number of overlapped hypermethylated DMRs between two datasets, indicating the reliability and relevance of these regions for cfDNA methylation biomarker discovery. We identified several candidate genes, including , , and , which have been previously established as liquid biopsy methylation biomarkers in various cancer types. Furthermore, we demonstrated the efficacy of targeted region analysis using cfDNA methylation data from oral cavity squamous cell carcinoma and nasopharyngeal carcinoma patients, further validating the utility of psDMR analysis in prioritizing cfDNA methylation biomarkers. Overall, our study contributes to the development of cfDNA-based approaches for early cancer detection and monitoring, expanding our understanding of the epigenetic landscape of HNSC, and providing valuable insights for liquid biopsy biomarker discovery not only in HNSC and other cancer types.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10327111PMC
http://dx.doi.org/10.1101/2023.06.27.546654DOI Listing

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