Department for Visceral, Thoracic and Vascular Surgery at the University Hospital, Technical University Dresden, Dresden, Germany.
Cancer Res. 2019 May 15;79(10):2462-2465. doi: 10.1158/0008-5472.CAN-19-0019. Epub 2019 May 1.
Cancer is one of the leading causes of death worldwide. This life-threatening disease requires novel strategies for the early detection and therapy response prediction. Circulating DNA was first described 70 years ago. However, only the recent evolution in the PCR-based sequencing techniques allow the minimally invasive molecular profiling of circulating mutant DNA from small-volume "liquid biopsies" such as blood, urine, or saliva. In this article, we aim to summarize the fast-growing evidence for cfDNA and exosomal DNA as minimally invasive diagnostic markers in solid tumors and to highlight their opposing diagnostic advantages and disadvantages.
癌症是全球主要死因之一。这种危及生命的疾病需要新的策略来进行早期检测和治疗反应预测。循环 DNA 最早在 70 年前被描述。然而,只有基于 PCR 的测序技术的最新发展,才能对来自血液、尿液或唾液等小体积“液体活检”的循环突变 DNA 进行微创的分子分析。在本文中,我们旨在总结 cfDNA 和外泌体 DNA 作为实体瘤微创诊断标志物的快速增长证据,并突出它们在诊断方面的优势和劣势。