外体
适体
生物标志物
诊断生物标志物
微泡
生物标志物发现
液体活检
计算生物学
癌症
医学
生物信息学
癌症研究
小RNA
生物
内科学
生物化学
分子生物学
基因
蛋白质组学
作者
Haolin Chen,Chuwen Huang,Yonglei Wu,Nianrong Sun,Chunhui Deng
出处
期刊:ACS Nano
[American Chemical Society]
日期:2022-08-10
卷期号:16 (8): 12952-12963
被引量:48
标识
DOI:10.1021/acsnano.2c05355
摘要
Gastric cancer (GC) presents high mortality worldwide because of delayed diagnosis. Currently, exosome-based liquid biopsy has been applied in diagnosis and monitoring of diseases including cancers, whereas disease detection based on exosomes at the metabolic level is rarely reported. Herein, the specific aptamer-coupled Au-decorated polymorphic carbon (CoMPC@Au-Apt) is constructed for the capture of urinary exosomes from early GC patients and healthy controls (HCs) and the subsequent exosome metabolic pattern profiling without extra elution process. Combining with machine learning algorithm on all exosome metabolic patterns, the early GC patients are excellently discriminated from HCs, with an accuracy of 100% for both the discovery set and blind test. Ulteriorly, three key metabolic features with clear identities are determined as a biomarker panel, obtaining a more than 90% diagnostic accuracy for early GC in the discovery set and validation set. Moreover, the change law of the key metabolic features along with GC development is revealed through making a comparison among HCs and GC at early stage and advanced stage, manifesting their monitoring ability toward GC. This work illustrates the high specificity of exosomes and the great prospective of exosome metabolic analysis in disease diagnosis and monitoring, which will promote exosome-driven precision medicine toward practical clinical application.
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