4.7 Review

Epigenetic Landscape of Liquid Biopsy in Colorectal Cancer

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2021.622459

Keywords

epigenetics; liquid biopsy; biomarkers; colorectal cancer; precision oncology; circulating nucleic acids; CTCs; extracellular vesicles

Funding

  1. ISCIII [PI18/00307, JR17/00016, FI19/00240]
  2. European Regional Development Fund (FEDER)
  3. Fondo Social Europeo (FSE)
  4. Roche-Chus Joint Unit - GAIN, Conselleria de Economia, Emprego e Industria [IN853B 2018/03]
  5. Xunta de Galicia [IN606A-2020/004]
  6. AECC

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Colorectal cancer is a common malignancy with high mortality rates, emphasizing the importance of improving early detection and personalized therapy. Liquid biopsy has emerged as a significant approach for identifying molecular alterations in CRC patients, including disruptions in epigenetic mechanisms. These epigenetic changes found in liquid biopsies have important implications for early detection, prognosis, monitoring, and evaluation of therapeutic response in CRC patients.
Colorectal cancer (CRC) is one of the most common malignancies and is a major cause of cancer-related deaths worldwide. Thus, there is a clinical need to improve early detection of CRC and personalize therapy for patients with this disease. In the era of precision oncology, liquid biopsy has emerged as a major approach to characterize the circulating tumor elements present in body fluids, including cell-free DNA and RNA, circulating tumor cells, and extracellular vesicles. This non-invasive tool has allowed the identification of relevant molecular alterations in CRC patients, including some indicating the disruption of epigenetic mechanisms. Epigenetic alterations found in solid and liquid biopsies have shown great utility as biomarkers for early detection, prognosis, monitoring, and evaluation of therapeutic response in CRC patients. Here, we summarize current knowledge of the most relevant epigenetic mechanisms associated with cancer development and progression, and the implications of their deregulation in cancer cells and liquid biopsy of CRC patients. In particular, we describe the methodologies used to analyze these epigenetic alterations in circulating tumor material, and we focus on the clinical utility of epigenetic marks in liquid biopsy as tumor biomarkers for CRC patients. We also discuss the great challenges and emerging opportunities of this field for the diagnosis and personalized management of CRC patients.

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