Department of Oncological Sciences, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Adv Exp Med Biol. 2022;1361:235-247. doi: 10.1007/978-3-030-91836-1_13.
In recent years, the rapid development of next-generation sequencing (NGS) has led to a significant increase in accuracy toward molecular profiling, allowing noninvasive and real-time detection of novel biomarkers for cancer screening and dynamic monitoring of disease development. Currently, the biggest challenge liquid biopsies face is the selection of the highest signal-bearing tissues (blood/urine or others) and components for diagnosis, being either circulating tumor cells (CTCs), circulating tumor DNA (ctDNA), or extracellular vesicles (EVs). This chapter describes the process of identifying cancer-associated molecular signals from liquid biopsies. First, we address strategies in selecting and processing samples for sequencing, and technical considerations involved in liquid biopsies under three settings: early detection, cancer diagnosis, and metastatic monitoring. Next, we discuss the methods and challenges to identify and validate prognostic signals, such as tumor burden or stage from CTC, targeted and nontargeted mutations from ctDNA, or noncoding RNAs from EVs. Finally, we review the current landscape of novel biomarkers and ongoing clinical trials for liquid biopsies to discuss the potential avenues for future precision medicine and clinical implementation.
近年来,下一代测序(NGS)的快速发展使得分子谱分析的准确性显著提高,能够无创实时检测癌症筛查的新型生物标志物,并动态监测疾病的发展。目前,液体活检面临的最大挑战是选择信号最强的组织(血液/尿液或其他)和成分进行诊断,这些成分可以是循环肿瘤细胞(CTC)、循环肿瘤 DNA(ctDNA)或细胞外囊泡(EVs)。本章描述了从液体活检中识别与癌症相关的分子信号的过程。首先,我们讨论了用于测序的样本选择和处理策略,以及在三种情况下(早期检测、癌症诊断和转移监测)进行液体活检时涉及的技术考虑因素。接下来,我们讨论了从 CTC 中识别和验证预后信号(如肿瘤负荷或分期)、从 ctDNA 中识别和验证靶向和非靶向突变、或从 EVs 中识别和验证非编码 RNA 的方法和挑战。最后,我们回顾了液体活检中新型生物标志物的现状和正在进行的临床试验,以讨论未来精准医学和临床实施的潜在途径。