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利用下一代测序技术对健康个体进行游离 DNA 分析:概念验证和技术验证研究。

Cell-free DNA analysis in healthy individuals by next-generation sequencing: a proof of concept and technical validation study.

机构信息

Institute of Pathology, University Hospital Basel, 4031, Basel, Switzerland.

Breast Cancer Unit and Translational Research Unit, ASST Cremona, Viale Concordia 1, 26100, Cremona, Italy.

出版信息

Cell Death Dis. 2019 Jul 11;10(7):534. doi: 10.1038/s41419-019-1770-3.

Abstract

Pre-symptomatic screening of genetic alterations might help identify subpopulations of individuals that could enter into early access prevention programs. Since liquid biopsy is minimally invasive it can be used for longitudinal studies in healthy volunteers to monitor events of progression from normal tissue to pre-cancerous and cancerous condition. Yet, cell-free DNA (cfDNA) analysis in healthy individuals comes with substantial challenges such as the lack of large cohort studies addressing the impact of mutations in healthy individuals or the low abundance of cfDNA in plasma. In this study, we aimed to investigate the technical feasibility of cfDNA analysis in a collection of 114 clinically healthy individuals. We first addressed the impact of pre-analytical factors such as cfDNA yield and quality on sequencing performance and compared healthy to cancer donor samples. We then confirmed the validity of our testing strategy by evaluating the mutational status concordance in matched tissue and plasma specimens collected from cancer patients. Finally, we screened our group of healthy donors for genetic alterations, comparing individuals who did not develop any tumor to patients who developed either a benign neoplasm or cancer during 1-10 years of follow-up time. To conclude, we have established a rapid and reliable liquid biopsy workflow that allowed us to study genomic alterations with a limit of detection as low as 0.08% of variant allelic frequency in healthy individuals. We detected pathogenic cancer mutations in four healthy donors that later developed a benign neoplasm or invasive breast cancer up to 10 years after blood collection. Even though larger prospective studies are needed to address the specificity and sensitivity of liquid biopsy as a clinical tool for early cancer detection, systematic screening of healthy individuals will help understanding early events of tumor formation.

摘要

在症状出现前对遗传改变进行筛查可能有助于确定能够进入早期预防计划的个体亚群。由于液体活检具有微创性,因此可以用于健康志愿者的纵向研究,以监测从正常组织到癌前和癌性状态的进展事件。然而,在健康个体中进行游离细胞 DNA(cfDNA)分析存在重大挑战,例如缺乏大规模队列研究来解决健康个体中突变的影响,或者 cfDNA 在血浆中的丰度低。在这项研究中,我们旨在调查 cfDNA 分析在 114 名临床健康个体中的技术可行性。我们首先研究了 cfDNA 产量和质量等分析前因素对测序性能的影响,并比较了健康供体和癌症供体样本。然后,我们通过评估从癌症患者收集的匹配组织和血浆标本中的突变状态一致性来验证我们的测试策略的有效性。最后,我们对我们的健康供体组进行了遗传改变筛查,将在 1-10 年随访期间未发生任何肿瘤的个体与发生良性肿瘤或癌症的患者进行比较。总之,我们已经建立了一种快速可靠的液体活检工作流程,使我们能够在健康个体中研究基因组改变,检测下限低至 0.08%的变异等位基因频率。我们在四个健康供体中检测到了致病性癌症突变,这些供体在采血后 10 年内发展为良性肿瘤或浸润性乳腺癌。尽管需要更大的前瞻性研究来解决液体活检作为早期癌症检测的临床工具的特异性和敏感性,但对健康个体进行系统筛查将有助于了解肿瘤形成的早期事件。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c924/6624284/de0954c68d75/41419_2019_1770_Fig1_HTML.jpg

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