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

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          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.

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          Most cited references38

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          Metabolomic profiles delineate potential role for sarcosine in prostate cancer progression.

          Multiple, complex molecular events characterize cancer development and progression. Deciphering the molecular networks that distinguish organ-confined disease from metastatic disease may lead to the identification of critical biomarkers for cancer invasion and disease aggressiveness. Although gene and protein expression have been extensively profiled in human tumours, little is known about the global metabolomic alterations that characterize neoplastic progression. Using a combination of high-throughput liquid-and-gas-chromatography-based mass spectrometry, we profiled more than 1,126 metabolites across 262 clinical samples related to prostate cancer (42 tissues and 110 each of urine and plasma). These unbiased metabolomic profiles were able to distinguish benign prostate, clinically localized prostate cancer and metastatic disease. Sarcosine, an N-methyl derivative of the amino acid glycine, was identified as a differential metabolite that was highly increased during prostate cancer progression to metastasis and can be detected non-invasively in urine. Sarcosine levels were also increased in invasive prostate cancer cell lines relative to benign prostate epithelial cells. Knockdown of glycine-N-methyl transferase, the enzyme that generates sarcosine from glycine, attenuated prostate cancer invasion. Addition of exogenous sarcosine or knockdown of the enzyme that leads to sarcosine degradation, sarcosine dehydrogenase, induced an invasive phenotype in benign prostate epithelial cells. Androgen receptor and the ERG gene fusion product coordinately regulate components of the sarcosine pathway. Here, by profiling the metabolomic alterations of prostate cancer progression, we reveal sarcosine as a potentially important metabolic intermediary of cancer cell invasion and aggressivity.
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            De novo lipogenesis protects cancer cells from free radicals and chemotherapeutics by promoting membrane lipid saturation.

            Activation of de novo lipogenesis in cancer cells is increasingly recognized as a hallmark of aggressive cancers and has been implicated in the production of membranes for rapid cell proliferation. In the current report, we provide evidence that this activation has a more profound role. Using a mass spectrometry-based phospholipid analysis approach, we show that clinical tumor tissues that display the lipogenic phenotype show an increase in the degree of lipid saturation compared with nonlipogenic tumors. Reversal of the lipogenic switch in cancer cells by treatment with the lipogenesis inhibitor soraphen A or by targeting lipogenic enzymes with small interfering RNA leads to a marked decrease in saturated and mono-unsaturated phospholipid species and increases the relative degree of polyunsaturation. Because polyunsaturated acyl chains are more susceptible to peroxidation, inhibition of lipogenesis increases the levels of peroxidation end products and renders cells more susceptible to oxidative stress-induced cell death. As saturated lipids pack more densely, modulation of lipogenesis also alters lateral and transversal membrane dynamics as revealed by diffusion of membrane-targeted green fluorescent protein and by the uptake and response to doxorubicin. These data show that shifting lipid acquisition from lipid uptake toward de novo lipogenesis dramatically changes membrane properties and protects cells from both endogenous and exogenous insults. These findings provide important new insights into the role of de novo lipogenesis in cancer cells, and they provide a rationale for the use of lipogenesis inhibitors as antineoplastic agents and as chemotherapeutic sensitizers. ©2010 AACR.
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              Metabolic profiles of cancer cells.

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                Author and article information

                Journal
                J Extracell Vesicles
                J Extracell Vesicles
                ZJEV
                zjev20
                Journal of Extracellular Vesicles
                Taylor & Francis
                2001-3078
                2018
                07 May 2018
                : 7
                : 1
                : 1470442
                Affiliations
                [a ]CIC bioGUNE, Bizkaia Technology Park , Derio, Spain
                [b ]Department of Urology, Basurto University Hospital , Bilbao, Spain
                [c ]Centro de Investigación Biomédica en Red de Cáncer (CIBERONC)
                [d ]OWL Metabolomics, Bizkaia Technology Park , Derio, Spain
                [e ]Department of Pathology, Basurto University Hospital , Bilbao, Spain
                [f ]Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD)
                [g ]Ikerbasque, Basque foundation for science , Bilbao, Spain
                [h ]Biochemistry and Molecular Biology Department, University of the Basque Country (UPV/EHU) , Bilbao, Spain
                Author notes
                CONTACT Arkaitz Carracedo acarracedo@ 123456cicbiogune.es ; Juan M. Falcón-Pérez jfalcon@ 123456cicbiogune.es

                Marc Clos-Garcia, Ana Loizaga-Iriarte and Patricia Zuñiga-Garcia contributed equally to the work

                Author information
                http://orcid.org/0000-0002-0208-1372
                http://orcid.org/0000-0003-2194-234X
                Article
                1470442
                10.1080/20013078.2018.1470442
                5944373
                29760869
                523220d4-516f-4d1d-94b1-6c92b1d11e7b
                © 2018 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group on behalf of The International Society for Extracellular Vesicles.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 15 January 2018
                : 17 April 2018
                Page count
                Figures: 6, Tables: 2, References: 50, Pages: 16
                Funding
                Funded by: Fundación BBVA 10.13039/100007406
                Award ID: SAF2016-79381-R (FEDER/EU)
                Funded by: H2020 European Research Council 10.13039/100010663
                Award ID: 336343, PoC 754627
                Funded by: Instituto de Salud Carlos III 10.13039/501100004587
                Award ID: PI12/01604
                Funded by: Ministerio de Economía y Competitividad 10.13039/501100003329
                Award ID: SAF2015-66312
                Funded by: department of education of the Basque Government
                Award ID: IKERTALDE IT1106-16
                Funded by: Severo Ochoa Excellence Accreditation
                Award ID: SEV-2016-0644
                Funded by: Fundación Vasca de Innovación e Investigación Sanitarias, BIOEF
                Award ID: BIO15/CA/052
                Funded by: AECC J.P. Bizkaia and the Basque Department of Health
                Award ID: 2016111109
                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].
                Categories
                Research Article

                prostate,urine,exosomes,metabolomics,metabolism,biomarkers
                prostate, urine, exosomes, metabolomics, metabolism, biomarkers

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