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      Lipidomic Biomarkers in Polycystic Ovary Syndrome and Endometrial Cancer

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          Abstract

          Women with polycystic ovary syndrome (PCOS) are more likely to develop endometrial cancer (EC). The molecular mechanisms which increase the risk of EC in PCOS are unclear. Derangements in lipid metabolism are associated with EC, but there have been no studies, investigating if this might increase the risk of EC in PCOS. This was a cross-sectional study of 102 women in three groups of 34 (PCOS, EC and controls) at Nottingham University Hospital, UK. All participants had clinical assessments, followed by obtaining plasma and endometrial tissue samples. Lipidomic analyses were performed using liquid chromatography (LC) coupled with high resolution mass spectrometry (HRMS) and the obtained lipid datasets were screened using standard software and databases. Using multivariate data analysis, there were no common markers found for EC and PCOS. However, on univariate analyses, both PCOS and EC endometrial tissue samples showed a significant decrease in monoacylglycerol 24:0 and capric acid compared to controls. Further studies are required to validate these findings and investigate the potential role of monoacylglycerol 24:0 and capric acid in the link between PCOS with EC.

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          Most cited references22

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          Metabolic profiles of cancer cells.

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            Evaluating the association between endometrial cancer and polycystic ovary syndrome.

            Given the current lack of clarity in the published literature, we performed a systematic review of the literature to determine the exact strength of the association between polycystic ovary syndrome (PCOS) and endometrial cancer (EC). All published studies on the association between PCOS and EC identified through MEDLINE (1966-April 2011), EMBASE (1980-April 2011) and Cochrane (1998-April 2011). Original data were abstracted where available and summarized on a separate Microsoft Excel (2007) database for analysis. A total of 14 studies comparative and non-comparative were identified and included. The non-comparative and comparative data suggested that women with PCOS were more likely to develop EC. A meta-analyses of five comparative studies showed an increased risk of EC in women with an odds ratio of 2.89 with a 95% confidence interval of 1.52-5.48. Women with PCOS are about three times more likely to develop EC compared with women without it. This translates into a 9% lifetime risk of EC in Caucasian women with PCOS compared with 3% in women without it. Although most women (91%) with PCOS will not develop endometrial cancer, our study has shown that they are more likely at increased risk. More studies are required to clarify the exact molecular mechanisms, determine the best way of screening and preventing disease progression.
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              Anti-bacterial and anti-inflammatory properties of capric acid against Propionibacterium acnes: a comparative study with lauric acid.

              Propionibacterium acnes (P. acnes) is a commensal bacterium which is possibly involved in acne inflammation. The saturated fatty acid, lauric acid (C12:0) has been shown to possess antibacterial and anti-inflammatory properties against P. acnes. Little is known concerning the potential effects of its decanoic counterpart, capric acid (C10:0).
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                Author and article information

                Journal
                Int J Mol Sci
                Int J Mol Sci
                ijms
                International Journal of Molecular Sciences
                MDPI
                1422-0067
                03 July 2020
                July 2020
                : 21
                : 13
                : 4753
                Affiliations
                [1 ]Department of Obstetrics and Gynaecology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Cheras, Kuala Lumpur 56000, Malaysia; nasirshafiee@ 123456ukm.edu.my
                [2 ]Division of Advanced Materials and Healthcare Technologies School of Pharmacy, Centre for Analytical Bioscience, University of Nottingham, University Park, Nottingham NG7 2RD, UK; catherine.ortori@ 123456nottingham.ac.uk (C.A.O.); david.barrett@ 123456nottingham.ac.uk (D.A.B.)
                [3 ]University of Nottingham Biodiscovery Institute, University of Nottingham LE12 5RD, UK; svznpm@ 123456exmail.nottingham.ac.uk
                [4 ]School of Veterinary Medicine and Science, University of Nottingham LE12 5RD, UK
                [5 ]Department of Obstetrics and Gynaecology, City Hospital, Nottingham University Hospital, Nottingham NG5 1PB, UK; jafaru.abu@ 123456nuh.nhs.uk
                [6 ]Division of Obstetrics and Gynaecology and Child Health, School of Medicine, Faculty of Medicine and Health Sciences, University of Nottingham, Queen’s Medical Centre, Nottingham University Hospital, Derby Road, Nottingham NG7 2UH, UK
                Author notes
                Author information
                https://orcid.org/0000-0001-5631-5309
                Article
                ijms-21-04753
                10.3390/ijms21134753
                7370092
                32635401
                c5fd5345-f5f1-4f69-abd7-c09936f5376d
                © 2020 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 07 May 2020
                : 29 June 2020
                Categories
                Article

                Molecular biology
                endometrial cancer,lipidomic,biomarkers,pcos
                Molecular biology
                endometrial cancer, lipidomic, biomarkers, pcos

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