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无融合,用于癌症诊断的小型细胞外囊泡 miRNA 的多重检测。

, Fusion-Free, Multiplexed Detection of Small Extracellular Vesicle miRNAs for Cancer Diagnostics.

机构信息

Department of Laboratory Medicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China.

Institute of Molecular Medicine, Shanghai Key Laboratory for Nucleic Acid Chemistry and Nanomedicine, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai 200127, China.

出版信息

Anal Chem. 2024 Oct 1;96(39):15665-15673. doi: 10.1021/acs.analchem.4c03129. Epub 2024 Sep 19.

Abstract

Tumor-derived small extracellular vesicle (sEV) microRNAs (miRNAs) are emerging biomarkers for cancer diagnostics. Conventional sEV miRNA detection methods necessitate the lysis of sEVs, rendering them laborious and time-consuming and potentially leading to damage or loss of miRNAs. Membrane fusion-based detection of sEV miRNAs involves the preparation of probe-loaded vesicles (, liposomes or cellular vesicles), which are typically sophisticated and require specialist equipment. Membrane perforation methods employ chemical treatments that can induce severe miRNA degradation or leaks. Inspired by previous studies that loaded nucleic acids into EVs or cells using hydrophobic tethers for therapeutic applications, herein, we repurposed this strategy by conjugating a hydrophobic tether onto molecular beacons to aid their transportation into sEVs, allowing for detection of miRNAs in a fusion-free and multiplexing manner. This method enables simultaneous detection of multiple miRNA species within serum-derived sEVs for the diagnosis of prostate cancer, breast cancer, and gastric cancer with an accuracy of 83.3%, 81.8%, and 100%, respectively, in a cohort of 66 individuals, indicating that it holds a high application potential in clinical diagnostics.

摘要

肿瘤来源的小细胞外囊泡 (sEV) 微 RNA (miRNA) 正在成为癌症诊断的新兴生物标志物。传统的 sEV miRNA 检测方法需要裂解 sEV,这既繁琐又耗时,并且可能导致 miRNA 的损伤或丢失。基于膜融合的 sEV miRNA 检测涉及探针加载囊泡(如脂质体或细胞囊泡)的制备,这通常很复杂,需要专业设备。膜穿孔方法采用化学处理,可能会导致严重的 miRNA 降解或泄漏。受先前研究的启发,这些研究使用疏水连接物将核酸载入 EVs 或细胞中,用于治疗应用,本文中,我们通过将疏水连接物连接到分子信标上来重新利用这种策略,以帮助它们进入 sEV,从而实现无融合和多重检测 miRNA。该方法能够在血清来源的 sEV 中同时检测多种 miRNA 种类,用于前列腺癌、乳腺癌和胃癌的诊断,在 66 名个体的队列中分别具有 83.3%、81.8%和 100%的准确性,表明其在临床诊断中有很高的应用潜力。

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