Rodriguez-Casanova Aitor, Costa-Fraga Nicolás, Bao-Caamano Aida, López-López Rafael, Muinelo-Romay Laura, Diaz-Lagares Angel
Cancer Epigenomics Laboratory, Translational Medical Oncology Group (Oncomet), Health Research Institute of Santiago (IDIS), University Clinical Hospital of Santiago (CHUS/SERGAS), Santiago de Compostela, Spain.
Roche-Chus Joint Unit, Translational Medical Oncology Group (Oncomet), Health Research Institute of Santiago (IDIS), Santiago de Compostela, Spain.
Front Cell Dev Biol. 2021 Feb 5;9:622459. doi: 10.3389/fcell.2021.622459. eCollection 2021.
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.
结直肠癌(CRC)是最常见的恶性肿瘤之一,也是全球癌症相关死亡的主要原因。因此,临床上需要改进CRC的早期检测,并为该疾病患者提供个性化治疗。在精准肿瘤学时代,液体活检已成为一种主要方法,用于表征体液中存在的循环肿瘤成分,包括游离DNA和RNA、循环肿瘤细胞和细胞外囊泡。这种非侵入性工具能够识别CRC患者的相关分子改变,包括一些表明表观遗传机制破坏的改变。在实体活检和液体活检中发现的表观遗传改变,作为CRC患者早期检测、预后、监测和治疗反应评估的生物标志物,已显示出巨大的应用价值。在此,我们总结了与癌症发生和进展相关的最相关表观遗传机制的当前知识,以及它们在癌细胞中的失调和CRC患者液体活检中的意义。特别是,我们描述了用于分析循环肿瘤物质中这些表观遗传改变的方法,并重点关注液体活检中表观遗传标记作为CRC患者肿瘤生物标志物的临床应用价值。我们还讨论了该领域在CRC患者诊断和个性化管理方面面临的巨大挑战和新出现的机遇。