Isolation and Quantification of Methylated Cell-Free DNA in Plasma on an Integrated Microfluidic System

化学 DNA甲基化 胎儿游离DNA CpG站点 生物标志物 甲基化 微流控 检出限 DNA 液体活检 甲基化DNA免疫沉淀 聚合酶链反应 计算生物学 癌症 分子生物学 色谱法 基因 生物化学 纳米技术 遗传学 基因表达 生物 产前诊断 怀孕 胎儿 材料科学
作者
Yu‐Jen Cheng,Chih‐Hung Wang,Keng‐Fu Hsu,Gwo‐Bin Lee
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:94 (4): 2134-2141 被引量:7
标识
DOI:10.1021/acs.analchem.1c04471
摘要

Methylated cell-free DNA (cfDNA) has been deemed a promising biomarker for ovarian cancer (OvCa) prognosis and therapy selection. However, exploring the methylation profiles of tumor suppressor genes in cfDNA remains a challenge due to their extremely low concentrations and complicated protocols, as well as methodological constraints. In this study, an integrated microfluidic system was developed to automatically (1) capture methylated cfDNA in plasma by magnetic beads coated with the methyl-CpG-binding domain and (2) quantify the methylation level of tumor suppressor genes by on-chip quantitative polymerase chain reaction (qPCR). For capturing methylated cfDNA from a very small amount of plasma, samples along with beads were mixed in a new micromixer to enhance the capture rate. With a high capture rate (72%) and a limit of quantification of 0.1 pg/μL (3 orders of magnitude lower than that of the benchtop method), the compact system could detect the methylated cfDNA from only 20 μL of plasma sample in 2 h. Furthermore, the dynamic range, from 0.1 to 2000 pg/μL of methylated cfDNA, spans the physiological range in plasma, signifying that this device has great potential for personalized medicine in OvCa.

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