Metabolic alterations in urine extracellular vesicles are associated to prostate cancer pathogenesis and progression

J Extracell Vesicles. 2018 May 7;7(1):1470442. doi: 10.1080/20013078.2018.1470442. eCollection 2018.

Abstract

Urine contains extracellular vesicles (EVs) that concentrate molecules and protect them from degradation. Thus, isolation and characterisation of urinary EVs could increase the efficiency of biomarker discovery. We have previously identified proteins and RNAs with differential abundance in urinary EVs from prostate cancer (PCa) patients compared to benign prostate hyperplasia (BPH). Here, we focused on the analysis of the metabolites contained in urinary EVs collected from patients with PCa and BPH. Targeted metabolomics analysis of EVs was performed by ultra-high-performance liquid chromatography-mass spectrometry. The correlation between metabolites and clinical parameters was studied, and metabolites with differential abundance in PCa urinary EVs were detected and mapped into cellular pathways. We detected 248 metabolites belonging to different chemical families including amino acids and various lipid species. Among these metabolites, 76 exhibited significant differential abundance between PCa and BPH. Interestingly, urine EVs recapitulated many of the metabolic alterations reported in PCa, including phosphathidylcholines, acyl carnitines, citrate and kynurenine. Importantly, we found elevated levels of the steroid hormone, 3beta-hydroxyandros-5-en-17-one-3-sulphate (dehydroepiandrosterone sulphate) in PCa urinary EVs, in line with the potential elevation of androgen synthesis in this type of cancer. This work supports urinary EVs as a non-invasive source to infer metabolic changes in PCa.

Keywords: Prostate; biomarkers; exosomes; metabolism; metabolomics; urine.

Grants and funding

The work of JF-P is supported by ISCIII [PI12/01604], Spanish Ministry of Economy and Competitiveness MINECO [SAF2015-66312] and GAP1 Movember Foundation. The work of A.C. is supported by the department of education of the Basque Government [IKERTALDE IT1106-16], the BBVA foundation, the MINECO [SAF2016-79381-R (FEDER/EU)]; European Research Council [Starting Grant 336343, PoC 754627]. The participation of A.C., A.R.C and V.T. as part of CIBERONC was co-funded with FEDER funds. V.T. is founded by Fundación Vasca de Innovación e Investigación Sanitarias, BIOEF [BIO15/CA/052], the AECC J.P. Bizkaia and the Basque Department of Health [2016111109]. We thank MINECO for the REDIEX (Spanish Excellence Network in Exosomes) and the Severo Ochoa Excellence Accreditation [SEV-2016-0644].