Suppr超能文献

两步竞争杂交分析检测法:一种分析细胞外囊泡中癌症相关 microRNA 的方法。

Two-Step Competitive Hybridization Assay: A Method for Analyzing Cancer-Related microRNA Embedded in Extracellular Vesicles.

机构信息

School of Biomedical Engineering, McMaster University, 1280 Main Street West, Hamilton, Ontario L8S 4L7, Canada.

Fraunhofer Institute for Cell Therapy and Immunology IZI, Leipzig 04103, Germany.

出版信息

Anal Chem. 2021 Dec 7;93(48):15913-15921. doi: 10.1021/acs.analchem.1c03165. Epub 2021 Nov 22.

Abstract

With an increased understanding of the role of microRNAs (miRNAs) in cancer evolution, there is a growing interest in the use of these non-coding nucleic acids in cancer diagnosis, prognosis, and treatment monitoring. miRNAs embedded in extracellular vesicles (EVs) are of particular interest given that circulating EVs carry cargo that are strongly correlated to their cells of origin such as tumor cells while protecting them from degradation. As such, there is a tremendous interest in new simple-to-operate vesicular microRNA analysis tools for widespread use in performing liquid biopsies. Herein, we present a two-step competitive hybridization assay that is rationally designed to translate low microRNA concentrations to large electrochemical signals as the measured signal is inversely proportional to the microRNA concentration. Using this assay, with a limit-of-detection of 122 aM, we successfully analyzed vesicular miRNA 200b from prostate cancer cell lines and human urine samples, demonstrating the expected lower expression levels of miRNA 200b in the EVs from prostate cancer cells and in the prostate cancer patient's urine samples compared to healthy patients and non-tumorigenic cell lines, validating the suitability of our approach for clinical analysis.

摘要

随着人们对 microRNAs(miRNAs)在癌症进化中作用的认识不断提高,人们越来越感兴趣地将这些非编码核酸应用于癌症诊断、预后和治疗监测。鉴于细胞外囊泡(EVs)中嵌入的 miRNA,由于循环 EV 携带与其起源细胞(如肿瘤细胞)强烈相关的货物,同时保护它们免受降解,因此,人们对新型简单操作的囊泡 microRNA 分析工具产生了浓厚的兴趣,以便广泛用于进行液体活检。在此,我们提出了一种两步竞争杂交测定法,该测定法经过合理设计,可将低浓度的 microRNA 转化为大的电化学信号,因为测量信号与 microRNA 浓度成反比。使用该测定法,检测限为 122 aM,我们成功地分析了前列腺癌细胞系和人尿液样本中的囊泡 miRNA 200b,与健康患者和非肿瘤细胞系相比,证实了来自前列腺癌细胞和前列腺癌患者尿液样本中的 miRNA 200b 的表达水平较低,验证了我们的方法适用于临床分析。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验