多路复用
数字聚合酶链反应
液体活检
克拉斯
化学
分子生物学
冷PCR
DNA
突变体
多重聚合酶链反应
分析灵敏度
聚合酶链反应
实时聚合酶链反应
癌症研究
癌症
突变
基因
病理
生物
点突变
生物化学
遗传学
医学
替代医学
作者
Erica D. Pratt,Robert W. Cowan,Sara L. Manning,Edmund Men Qiao,Heather Cameron,Kara A. Schradle,Diane M. Simeone,David Bing Zhen
标识
DOI:10.1021/acs.analchem.8b01605
摘要
Oncology research is increasingly incorporating molecular detection of circulating tumor DNA (ctDNA) as a tool for cancer surveillance and early detection. However, noninvasive monitoring of conditions with low tumor burden remains challenging, as the diagnostic sensitivity of most ctDNA assays is inversely correlated with total DNA concentration and ctDNA abundance. Here we present the Multiplex Enrichment using Droplet Pre-Amplification (MED-Amp) method, which combines single-molecule emulsification and short-round polymerase chain reaction (PCR) preamplification with digital droplet PCR detection of mutant DNA template. The MED-Amp assay increased mutant signal by over 50-fold with minimal distortion in allelic frequency. We demonstrate detection of as few as three mutant copies in wild-type DNA concentrations ranging from 5 to 50 ng. The MED-Amp assay successfully detected KRAS mutant ctDNA in 86% plasma samples obtained from patients with metastatic pancreatic ductal adenocarcinoma. This assay for high-sensitivity rare variant detection is appropriate for liquid biopsy samples or other limited clinical biospecimens.
科研通智能强力驱动
Strongly Powered by AbleSci AI