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Ossoliński et al. J Cancer Metastasis Treat 2019;5:1                Journal of Cancer
               DOI: 10.20517/2394-4722.2018.63                           Metastasis and Treatment




               Original Article                                                              Open Access


               Mass spectrometry-based metabolomic profiling of
               prostate cancer - a pilot study


               Krzysztof Ossoliński , Joanna Nizioł , Adrian Arendowski , Anna Ossolińska , Tadeusz Ossoliński ,
                                 1#
                                                                                                    1
                                                                                  1
                                               2#
                                                                  2
               Jakub Kucharz , Paweł Wiechno , Tomasz Ruman 2
                            3
                                           3
               1 Department of Urology, John Paul II Hospital, Kolbuszowa 36-100, Poland.
               2 Faculty of Chemistry, Rzeszów University of Technology, Rzeszów 35-959, Poland.
               3 Department of Urooncology, Institute of Oncology, Warsaw 02-781, Poland.
               # Authors contributed equally.
               Correspondence to: Dr. Tomasz Ruman, Faculty of Chemistry, Rzeszów University of Technology, al. Powstanców Warszawy 6,
               Rzeszów 35-959, Poland. E-mail: tomruman@prz.edu.pl
               How to cite this article: Ossoliński K, Nizioł J, Arendowski A, Ossolińska A, Ossoliński T, Kucharz J, Wiechno P, Ruman T. Mass
               spectrometry-based metabolomic profiling of prostate cancer - a pilot study. J Cancer Metastasis Treat 2019;5:1.
               http://dx.doi.org/10.20517/2394-4722.2018.63
               Received: 22 Sep 2018    First Decision: 19 Nov 2018    Revised: 17 Dec 2018    Accepted: 19 Dec 2018    Published: 8 Jan 2019

               Science Editor: Bing-Liang Fang    Copy Editor: Cui Yu    Production Editor: Huan-Liang Wu



               Abstract
               Aim: Prostate cancer (PCa) is the most commonly diagnosed non-skin cancer among men. Serum prostate-
               specific antigen level is used as a standard PCa biomarker for over 20 years. However, it has only 33% specificity
               and 86% sensitivity (for the cutoff value for prostate biopsy of > 4 ng/mL). This leads to overdiagnosis and
               overtreatment. In-depth insight into PCa metabolomics enables discovery of novel PCa biomarkers.

               Methods: Metabolomic alternation in PCa serum, urine and interstitial fluid was examined using gold-
               nanoparticle-based laser mass spectrometry imaging. This study included 5 patients who underwent prostate
               biopsy with positive result, 5 patients with negative result and 10 healthy controls.

               Results: Over two hundred differentiating metabolites (87 in urine, 54 in serum and 78 in interstitial fluid) were
               detected. Four, twenty two and ten metabolites from urine, serum and interstitial fluid respectively showed
               statistical significant differential abundance between cancer and control group.

               Conclusion: Comprehensive metabolomic profile of PCa has been identified. Out of 36 metabolites, 20 were
               identified and should be further evaluated in clinical trials as a potential PCa biomarker. Urine concentration of
               triglyceride (12:0/20:1) showed over 10 times higher abundance in PCa samples in comparison to healthy controls
               and is considered the most promising potential biomarker.


                           © The Author(s) 2019. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use,
                sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long
                as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
                and indicate if changes were made.


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