液体活检
多路复用
数字聚合酶链反应
肺癌
生物标志物
DNA甲基化
多重聚合酶链反应
甲基化
活检
计算生物学
循环肿瘤细胞
癌症
癌症研究
癌症生物标志物
亚硫酸氢盐测序
病理
肿瘤科
生物
医学
聚合酶链反应
DNA
内科学
基因
生物信息学
基因表达
遗传学
转移
作者
Yang Zhao,Christine M. O’Keefe,Kuangwen Hsieh,Leslie Cope,Sonali Joyce,Thomas R. Pisanic,James G. Herman,Tza‐Huei Wang
标识
DOI:10.1002/advs.202206518
摘要
Abstract There remains tremendous interest in developing liquid biopsy assays for detection of cancer‐specific alterations, such as mutations and DNA methylation, in cell‐free DNA (cfDNA) obtained through noninvasive blood draws. However, liquid biopsy analysis is often challenging due to exceedingly low fractions of circulating tumor DNA (ctDNA), necessitating the use of extended tumor biomarker panels. While multiplexed PCR strategies provide advantages such as higher throughput, their implementation is often hindered by challenges such as primer‐dimers and PCR competition. Alternatively, digital PCR (dPCR) approaches generally offer superior performance, but with constrained multiplexing capability. This paper describes development and validation of the first multiplex digital methylation‐specific PCR (mdMSP) platform for simultaneous analysis of four methylation biomarkers for liquid‐biopsy‐based detection of non‐small cell lung cancer (NSCLC). mdMSP employs a microfluidic device containing four independent, but identical modules, housing a total of 40 160 nanowells. Analytical validation of the mdMSP platform demonstrates multiplex detection at analytical specificities as low as 0.0005%. The clinical utility of mdMSP is also demonstrated in a cohort of 72 clinical samples of low‐volume liquid biopsy specimens from patients with computed tomography (CT)‐scan indeterminant pulmonary nodules, exhibiting superior clinical performance when compared to traditional MSP assays for noninvasive detection of early‐stage NSCLC.
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