Encoded Fusion-Mediated MicroRNA Signature Profiling of Tumor-Derived Extracellular Vesicles for Pancreatic Cancer Diagnosis

被引:15
作者
Feng, Jianzhou [1 ,2 ]
Shu, Yun [2 ]
An, Yu [1 ]
Niu, Qi [3 ]
Fan, Qian [1 ]
Lei, Yanmei [1 ]
Gong, Yanli [1 ]
Hu, Xiaoya [2 ]
Zhang, Peng [1 ]
Liu, Yingbin [1 ]
Yang, Chaoyong [1 ,3 ]
Wu, Lingling [1 ]
机构
[1] Shanghai Jiao Tong Univ, Renji Hosp, Inst Mol Med, Sch Med,Shanghai Key Lab Nucleic Acid Chem & Nanom, Shanghai 200127, Peoples R China
[2] Yangzhou Univ, Sch Chem & Chem Engn, Yangzhou 225002, Jiangsu, Peoples R China
[3] Xiamen Univ, Coll Chem & Chem Engn, Dept Chem Biol, MOE Key Lab Spectrochem Anal & Instrumentat,Collab, Xiamen 361005, Fujian, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
BIOMARKERS;
D O I
10.1021/acs.analchem.3c00929
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
MicroRNAs (miRNAs) in tumor-derived extracellular vesicles (tEVs) are important cancer biomarkers for cancer screening and early diagnosis. Multiplex detection of miRNAs in tEVs facilitates accurate diagnosis but remains a challenge. Herein, we propose an encoded fusion strategy to profile the miRNA signature in tEVs for pancreatic cancer diagnosis. A panel of encoded-targeted-fusion beads was fabricated for the selective recognition and fusion of tEVs, with the turn-on fluorescence signals of molecule beacons for miRNA quantification and barcode signals for miRNA identification using readily accessible flow cytometers. Using this strategy, six types of pancreatic-cancer-associated miRNAs can be profiled in tEVs from 2 mu L plasma samples (n = 36) in an isolation-free and lysis-free manner with only 2 h of processing, offering a high accuracy (98%) to discriminate pancreatic cancer, pancreatitis, and healthy donors. This encoded fusion strategy exhibits great potential for multiplex profiling of miRNA in tEVs, offering new avenues for cancer diagnosis and screening.
引用
收藏
页码:7743 / 7752
页数:10
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