Johnston Andrew D, Ross Jason P, Ma Chenkai, Fung Kim Y C, Locke Warwick J
Human Health, Health and Biosecurity, CSIRO, Westmead, NSW, Australia.
Front Oncol. 2023 Apr 4;13:1103797. doi: 10.3389/fonc.2023.1103797. eCollection 2023.
Liquid biopsy assays for minimal residual disease (MRD) are used to monitor and inform oncological treatment and predict the risk of relapse in cancer patients. To-date, most MRD assay development has focused on targeting somatic mutations. However, epigenetic changes are more frequent and universal than genetic alterations in cancer and circulating tumor DNA (ctDNA) retains much of these changes. Here, we review the epigenetic signals that can be used to detect MRD, including DNA methylation alterations and fragmentation patterns that differentiate ctDNA from noncancerous circulating cell-free DNA (ccfDNA). We then summarize the current state of MRD monitoring; highlight the advantages of epigenetics over genetics-based approaches; and discuss the emerging paradigm of assaying both genetic and epigenetic targets to monitor treatment response, detect disease recurrence, and inform adjuvant therapy.
用于检测微小残留病(MRD)的液体活检检测方法可用于监测癌症患者的肿瘤治疗情况并提供相关信息,同时预测复发风险。迄今为止,大多数MRD检测方法的开发都集中在靶向体细胞突变上。然而,在癌症中,表观遗传变化比基因改变更为频繁和普遍,并且循环肿瘤DNA(ctDNA)保留了许多这些变化。在这里,我们综述了可用于检测MRD的表观遗传信号,包括区分ctDNA与非癌性循环游离DNA(ccfDNA)的DNA甲基化改变和片段化模式。然后,我们总结了MRD监测的现状;强调表观遗传学相对于基于遗传学方法的优势;并讨论了同时检测基因和表观遗传靶点以监测治疗反应、检测疾病复发及指导辅助治疗的新兴模式。