Center for Oncological Research Antwerp (CORE), University of Antwerp (UA), Wilrijk, Belgium.
Laboratory of Pathological Anatomy, Antwerp University Hospital (UZA), Edegem, Belgium.
PLoS One. 2020 Apr 6;15(4):e0231058. doi: 10.1371/journal.pone.0231058. eCollection 2020.
Although liquid biopsies offer many advantages over tissue biopsies, they are not yet standard practice. An important reason for the lack of implementation is the unavailability of well standardized techniques and guidelines, especially for pre-analytical conditions which are an important factor causing the current sensitivity issues. To overcome these limitations, we investigated the effect of several pre-analytical conditions on the concentration of cell-free DNA (cfDNA) and cellular genomic DNA (gDNA) contamination. Urine samples from healthy volunteers (HVs) and cancer patients were collected and processed according to specific pre-analytical conditions. Our results show that in samples with a relatively small volume more than 50% of the cfDNA can be found in the first 50 mL of the urine sample. The total DNA concentration increased again when samples were collected more than 3.5 hours apart. Adding preservative to urine samples is recommended to obtain high concentrations of cfDNA. To remove the cellular content, high speed centrifugation protocols as 4,000g 10min or 3,000g 15min are ideal for urine collected in cfDNA Urine Preserve (Streck). Although this study was a pilot study and needs to be confirmed in a larger study population, clear trends in the effect of several pre-analytical conditions were observed.
虽然液体活检相对于组织活检具有许多优势,但它们尚未成为标准实践。缺乏实施的一个重要原因是缺乏标准化的技术和指南,特别是对于分析前条件,这是导致当前灵敏度问题的重要因素。为了克服这些限制,我们研究了几种分析前条件对游离 DNA(cfDNA)和细胞基因组 DNA(gDNA)污染浓度的影响。从健康志愿者(HV)和癌症患者中采集尿液样本,并根据特定的分析前条件进行处理。我们的结果表明,在体积较小的样本中,超过 50%的 cfDNA 可以在前 50 毫升的尿液样本中找到。当样本采集间隔超过 3.5 小时时,总 DNA 浓度再次增加。建议向尿液样本中添加防腐剂以获得高浓度的 cfDNA。为了去除细胞内容物,对于在 cfDNA 尿液保存液(Streck)中收集的尿液,4000g 10min 或 3000g 15min 的高速离心方案是理想的。虽然这项研究是一项初步研究,需要在更大的研究人群中得到证实,但观察到了几种分析前条件的影响的明显趋势。