细胞外小泡
全内反射荧光显微镜
小RNA
乳腺癌
癌症
计算生物学
胞外囊泡
癌症生物标志物
微泡
生物
癌症研究
人工智能
细胞生物学
医学
病理
计算机科学
内科学
基因
遗传学
显微镜
作者
Xuewei Zhang,Gong-Xiang Qi,Meng-Xian Liu,Yanfei Yang,Jianhua Wang,Yong‐Liang Yu,Shuai Chen
出处
期刊:ACS Sensors
[American Chemical Society]
日期:2024-03-05
卷期号:9 (3): 1555-1564
被引量:16
标识
DOI:10.1021/acssensors.3c02789
摘要
Extracellular vesicle microRNAs (EV miRNAs) are critical noninvasive biomarkers for early cancer diagnosis. However, accurate cancer diagnosis based on bulk analysis is hindered by the heterogeneity among EVs. Herein, we report an approach for profiling single-EV multi-miRNA signatures by combining total internal reflection fluorescence (TIRF) imaging with a deep learning (DL) algorithm for the first time. This innovative technique allows for the precise characterization of EV miRNAs at the single-vesicle level, overcoming the challenges posed by EV heterogeneity. TIRF with high resolution and a signal-to-noise ratio can simultaneously detect multi-miRNAs in situ in individual EVs. DL algorithm avoids complicated and inaccurate artificial feature extraction, achieving automated high-resolution image analysis. Using this approach, we reveal that the main variation of EVs from 5 cancer cells and normal plasma is the triple-positive EV subpopulation, and the classification accuracy of single triple-positive EVs from 6 sources can reach above 95%. In the clinical cohort, 20 patients (5 lung cancer, 5 breast cancer, 5 cervical cancer, and 5 colon cancer) and 5 healthy controls are predicted with an overall accuracy of 100%. This single-EV strategy provides new opportunities for exploring more specific EV biomarkers to achieve cancer diagnosis and classification.
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