生物标志物
多路复用
化学
CD63
核糖核酸
分子生物学
外体
胞外囊泡
分子信标
胰腺癌
细胞外小泡
癌症生物标志物
微泡
DNA
计算生物学
癌症
小RNA
细胞生物学
寡核苷酸
生物化学
基因
生物
生物信息学
遗传学
作者
Jie He,Jiang Long,Chunhui Zhai,Jiasu Xu,Kaiwen Bao,Wenqiong Su,Lai Jiang,Guangxia Shen,Xianting Ding
标识
DOI:10.1021/acs.analchem.3c05858
摘要
Tumor-derived extracellular vesicles (EVs) carry tumor-specific proteins and RNAs, thus becoming prevalent targets for early cancer diagnosis. However, low expression of EV cargos and insufficient diagnostic power of individual biomarkers hindered EVs application in clinical practice. Herein, we propose a multiplex Codetection platform of proteins and RNAs (Co-PAR) for EVs. Co-PAR adopted a pair of antibody-DNA probes to recognize the same target protein, which in turn formed a double-stranded DNA. Thus, the target protein could be quantified by detecting the double-stranded DNA via qPCR. Meanwhile, qRT-PCR simultaneously quantified the target RNAs. Thus, with a regular qPCR instrument, Co-PAR enabled the codetection of multiplex proteins and RNAs, with the sensitivity of 102 EVs/μL (targeting CD63) and 1 EV/μL (targeting snRNA U6). We analyzed the coexpressions of three protein markers (CD63, GPC-1, HER2) and three RNA markers (snRNA U6, GPC-1 mRNA, miR-10b) on EVs from three pancreatic cell lines and 30 human plasma samples using Co-PAR. The diagnostic accuracy of the 6-biomarker combination reached 92.9%, which was at least 6.2% higher than that of 3-biomarker combinations and at least 13.5% higher than that of 6 single biomarkers. Co-PAR, as a multiparameter detection platform for EVs, has great potential in early disease diagnosis.
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