Institute of Biomedical Research, Sapporo Higashi Tokushukai Hospital, Hokkaido, Japan.
Department of Medicine, Asahikawa Medical University, Japan.
Mol Oncol. 2017 Oct;11(10):1448-1458. doi: 10.1002/1878-0261.12110. Epub 2017 Aug 8.
Genetic alterations responsible for the initiation of cancer may serve as immediate biomarkers for early diagnosis. Plasma levels of cell-free DNA (cfDNA) in patients with cancer are higher than those in healthy individuals; however, the major technical challenge for the widespread implementation of cfDNA genotyping as a diagnostic tool is the insufficient sensitivity and specificity of detecting early-stage tumors that shed low amounts of cfDNA. To establish a protocol for ultrasensitive droplet digital polymerase chain reaction (ddPCR) for quantification of low-frequency alleles within a limited cfDNA pool, two-step multiplex ddPCR targeting eight clinically relevant mutant KRAS variants was examined. Plasma samples from patients with colorectal (n = 10) and pancreatic cancer (n = 9) were evaluated, and cfDNA from healthy volunteers (n = 50) was utilized to calculate reference intervals. Limited cfDNA yields in patients with resectable colorectal and pancreatic cancers did not meet the requirement for efficient capture and quantification of rate mutant alleles by ddPCR. Eight preamplification cycles followed by a second-run ddPCR were sufficient to obtain approximately 5000-10 000 amplified copies per ng of cfDNA, resolving the subsampling issue. Furthermore, the signal-to-noise ratio for rare mutant alleles against the extensive background presented by the wild-type allele was significantly enhanced. The cutoff limit of reference intervals for mutant KRAS was determined to be ~ 0.09% based on samples from healthy individuals. The modification introduced in the ddPCR protocol facilitated the quantification of low-copy alleles carrying driver mutations, such as oncogenic KRAS, in localized and early-stage cancers using small blood volumes, thus offering a minimally invasive modality for timely diagnosis.
导致癌症发生的遗传改变可以作为早期诊断的即时生物标志物。癌症患者血浆中无细胞游离 DNA (cfDNA) 的水平高于健康个体;然而,cfDNA 基因分型作为诊断工具广泛应用的主要技术挑战是检测脱落低量 cfDNA 的早期肿瘤的灵敏度和特异性不足。为了建立一种用于超灵敏液滴数字聚合酶链反应 (ddPCR) 定量有限 cfDNA 池内低频等位基因的方案,研究了两步多重 ddPCR 靶向八个临床相关突变 KRAS 变体。评估了来自结直肠癌 (n = 10) 和胰腺癌 (n = 9) 患者的血浆样本,并利用来自健康志愿者 (n = 50) 的 cfDNA 计算参考区间。可切除结直肠癌和胰腺癌患者的有限 cfDNA 产量不符合 ddPCR 有效捕获和定量突变等位基因的要求。在前扩增 8 个循环后进行第二轮 ddPCR,足以获得每个 ng cfDNA 约 5000-10000 个扩增拷贝,解决了亚采样问题。此外,稀有突变等位基因与野生型等位基因呈现的广泛背景之间的信噪比显著提高。根据健康个体的样本,将突变 KRAS 的参考区间截断限确定为约 0.09%。ddPCR 方案中的修改促进了使用小体积血液对携带驱动突变(如致癌 KRAS)的低拷贝等位基因进行定量,从而为及时诊断提供了一种微创方式。