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从前列腺癌患者尿液中分离和表征微囊泡:不同的方法,不同的视角。

Isolation and characterization of urine microvesicles from prostate cancer patients: different approaches, different visions.

机构信息

Laboratory of Molecular Biology, Fundación Instituto Valenciano de Oncología, 46009, Valencia, Spain.

IVO-CIPF Joint Research Unit of Cancer, Príncipe Felipe Research Center (CIPF), 46012, Valencia, Spain.

出版信息

BMC Urol. 2021 Sep 27;21(1):137. doi: 10.1186/s12894-021-00902-8.

Abstract

BACKGROUND

Because of their specific and biologically relevant cargo, urine extracellular vesicles (EVs) constitute a valuable source of potential non-invasive biomarkers that could support the clinical decision-making to improve the management of prostate cancer (PCa) patients. Different EV isolation methods differ in terms of complexity and yield, conditioning, as consequence, the analytical result.

METHODS

The aim of this study was to compare three different isolation methods for urine EVs: ultracentrifugation (UC), size exclusion chromatography (SEC), and a commercial kit (Exolute® Urine Kit). Urine samples were collected from 6 PCa patients and 4 healthy donors. After filtered through 0.22 µm filters, urine was divided in 3 equal volumes to perform EVs isolation with each of the three approaches. Isolated EVs were characterized by spectrophotometric protein quantification, nanoparticle tracking analysis, transmission electron microscopy, AlphaScreen Technology, and whole miRNA Transcriptome.

RESULTS

Our results showed that UC and SEC provided better results in terms of EVs yield and purity than Exolute®, non-significant differences were observed in terms of EV-size. Interestingly, luminescent AlphaScreen assay demonstrated a significant enrichment of CD9 and CD63 positive microvesicles in SEC and UC methods compared with Exolute®. This heterogeneity was also demonstrated in terms of miRNA content indicating that the best correlation was observed between UC and SEC.

CONCLUSIONS

Our study highlights the importance of standardizing the urine EV isolation methods to guaranty the analytical reproducibility necessary for their implementation in a clinical setting.

摘要

背景

由于其具有特定的生物学相关内容,尿液细胞外囊泡(EVs)构成了有潜在非侵入性生物标志物的宝贵来源,可支持临床决策,以改善前列腺癌(PCa)患者的管理。不同的 EV 分离方法在复杂性和产量方面存在差异,因此会影响分析结果。

方法

本研究旨在比较三种不同的尿液 EV 分离方法:超速离心(UC)、尺寸排阻色谱(SEC)和商用试剂盒(Exolute®尿液试剂盒)。收集 6 名 PCa 患者和 4 名健康供体的尿液样本。尿液样本经 0.22μm 过滤器过滤后,等分 3 份,分别用三种方法进行 EVs 分离。通过分光光度法蛋白定量、纳米颗粒跟踪分析、透射电子显微镜、AlphaScreen 技术和全 miRNA 转录组学对分离出的 EVs 进行表征。

结果

我们的结果表明,UC 和 SEC 在 EVs 产量和纯度方面的结果优于 Exolute®,但在 EV 大小方面无显著差异。有趣的是,发光 AlphaScreen 测定法显示,与 Exolute®相比,SEC 和 UC 方法中 CD9 和 CD63 阳性微囊泡的富集程度显著更高。这种异质性也表现在 miRNA 含量方面,表明 UC 和 SEC 之间的相关性最好。

结论

本研究强调了标准化尿液 EV 分离方法的重要性,以保证其在临床环境中的实施所需的分析重现性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/77f3/8477576/b916d6ae7996/12894_2021_902_Fig1_HTML.jpg

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