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从尿液中提取的前列腺分泌物外泌体的深入蛋白质组学分析。

In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.

机构信息

Ontario Cancer Institute, University Health Network, Toronto, Canada.

Department of Cell and Molecular Pharmacology and Experimental Therapeutics, Medical University of South Carolina, Charleston, SC, USA.

出版信息

Proteomics. 2013 May;13(10-11):1667-1671. doi: 10.1002/pmic.201200561. Epub 2013 Apr 23.

Abstract

Expressed prostatic secretions (EPS) are proximal fluids of the prostate that are increasingly being utilized as a clinical source for diagnostic and prognostic assays for prostate cancer (PCa). These fluids contain an abundant amount of microvesicles reflecting the secretory function of the prostate gland, and their protein composition remains poorly defined in relation to PCa. Using expressed prostatic secretions in urine (EPS-urine), exosome preparations were characterized by a shotgun proteomics procedure. In pooled EPS-urine exosome samples, ~900 proteins were detected. Many of these have not been previously observed in the soluble proteome of EPS generated by our labs or other related exosome proteomes. We performed systematic comparisons of our data against previously published, prostate-related proteomes, and global annotation analyses to highlight functional processes within the proteome of EPS-urine derived exosomes. The acquired proteomic data have been deposited to the Tranche repository and will lay the foundation for more extensive investigations of PCa derived exosomes in the context of biomarker discovery and cancer biology.

摘要

前列腺分泌物(EPS)是前列腺的近端液体,越来越多地被用作前列腺癌(PCa)诊断和预后检测的临床来源。这些液体中含有大量的微囊泡,反映了前列腺的分泌功能,其蛋白质组成与 PCa 的关系尚不清楚。本研究利用尿液中的前列腺分泌物(EPS-urine),通过鸟枪法蛋白质组学程序对其外泌体进行了表征。在 pooled EPS-urine 外泌体样本中,检测到约 900 种蛋白质。其中许多蛋白质以前没有在我们实验室或其他相关外泌体蛋白质组学生成的 EPS 可溶性蛋白质组中观察到。我们对数据进行了系统的比较,与以前发表的前列腺相关蛋白质组学以及全局注释分析进行了比较,以突出 EPS 衍生外泌体蛋白质组中的功能过程。获得的蛋白质组学数据已被存入 Tranche 存储库,为在生物标志物发现和癌症生物学背景下更广泛地研究 PCa 衍生的外泌体奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0ce3/3773505/ec534c140c88/nihms-502285-f0001.jpg

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