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
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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