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      Peritoneal Fluid Cytokines Reveal New Insights of Endometriosis Subphenotypes

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          Abstract

          Endometriosis is a common inflammatory gynecological disorder which causes pelvic scarring, pain, and infertility, characterized by the implantation of endometrial-like lesions outside the uterus. The peritoneum, ovaries, and deep soft tissues are the commonly involved sites, and endometriotic lesions can be classified into three subphenotypes: superficial peritoneal endometriosis (PE), ovarian endometrioma (OE), and deep infiltrating endometriosis (DIE). In 132 women diagnosed laparoscopically with and without endometriosis ( n = 73, 59 respectively), and stratified into PE, OE, and DIE, peritoneal fluids (PF) were characterized for 48 cytokines by using multiplex immunoassays. Partial-least-squares-regression analysis revealed distinct subphenotype cytokine signatures—a six-cytokine signature distinguishing PE from OE, a seven-cytokine signature distinguishing OE from DIE, and a six-cytokine-signature distinguishing PE from DIE—each associated with different patterns of biological processes, signaling events, and immunology. These signatures describe endometriosis better than disease stages ( p < 0.0001). Pathway analysis revealed the association of ERK1 and 2, AKT, MAPK, and STAT4 linked to angiogenesis, cell proliferation, migration, and inflammation in the subphenotypes. These data shed new insights on the pathophysiology of endometriosis subphenotypes, with the potential to exploit the cytokine signatures to stratify endometriosis patients for targeted therapies and biomarker discovery.

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          Most cited references70

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          Pathogenesis and pathophysiology of endometriosis.

          Originally described over three hundred years ago, endometriosis is classically defined by the presence of endometrial glands and stroma in extrauterine locations. Endometriosis is an inflammatory, estrogen-dependent condition associated with pelvic pain and infertility. This work reviews the disease process from theories regarding origin to the molecular basis for disease sequelae. A thorough understanding of the histopathogenesis and pathophysiology of endometriosis is essential to the development of novel diagnostic and treatment approaches for this debilitating condition. Copyright © 2012 American Society for Reproductive Medicine. All rights reserved.
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            Revised American Fertility Society classification of endometriosis: 1985.

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              The Pathogenesis of Endometriosis: Molecular and Cell Biology Insights

              The etiopathogenesis of endometriosis is a multifactorial process resulting in a heterogeneous disease. Considering that endometriosis etiology and pathogenesis are still far from being fully elucidated, the current review aims to offer a comprehensive summary of the available evidence. We performed a narrative review synthesizing the findings of the English literature retrieved from computerized databases from inception to June 2019, using the Medical Subject Headings (MeSH) unique ID term “Endometriosis” (ID:D004715) with “Etiology” (ID:Q000209), “Immunology” (ID:Q000276), “Genetics” (ID:D005823) and “Epigenesis, Genetic” (ID:D044127). Endometriosis may origin from Müllerian or non-Müllerian stem cells including those from the endometrial basal layer, Müllerian remnants, bone marrow, or the peritoneum. The innate ability of endometrial stem cells to regenerate cyclically seems to play a key role, as well as the dysregulated hormonal pathways. The presence of such cells in the peritoneal cavity and what leads to the development of endometriosis is a complex process with a large number of interconnected factors, potentially both inherited and acquired. Genetic predisposition is complex and related to the combined action of several genes with limited influence. The epigenetic mechanisms control many of the processes involved in the immunologic, immunohistochemical, histological, and biological aberrations that characterize the eutopic and ectopic endometrium in affected patients. However, what triggers such alterations is not clear and may be both genetically and epigenetically inherited, or it may be acquired by the particular combination of several elements such as the persistent peritoneal menstrual reflux as well as exogenous factors. The heterogeneity of endometriosis and the different contexts in which it develops suggest that a single etiopathogenetic model is not sufficient to explain its complex pathobiology.
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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
                15 May 2020
                May 2020
                : 21
                : 10
                : 3515
                Affiliations
                [1 ]Translational ‘Omics and Biomarkers group, KK Research Centre, KK Women’s and Children’s Hospital, Singapore 229899, Singapore; zhou.jieliang@ 123456kkh.com.sg
                [2 ]Division of Obstetrics and Gynaecology, KK Women’s and Children’s Hospital, Singapore 229899, Singapore; bernard.chern.s.m@ 123456singhealth.com.sg (B.S.M.C.); gmskcw@ 123456nus.edu.sg (C.W.K.)
                [3 ]OBGYN-Academic Clinical Program, Duke-NUS Medical School, Singapore 169857, Singapore; jessie.phoon.w.l@ 123456singhealth.com.sg (J.W.L.P.); tan.heng.hao@ 123456singhealth.com.sg (H.H.T.); jerry.chan.k.y@ 123456singhealth.com.sg (J.K.Y.C.)
                [4 ]Department of Obstetrics and Gynaecology, Singapore General Hospital, Singapore 169608, Singapore; pcbartonsmith@ 123456gmail.com
                [5 ]Department of Reproductive Medicine, KKH, Singapore 229899, Singapore; tan.tse.yeun@ 123456singhealth.com.sg (T.Y.T.); veronique.viardot@ 123456singhealth.com.sg (V.V.-F.)
                Author notes
                [* ]Correspondence: yiehou.lee@ 123456smart.mit.edu ; Tel.: +65-6238-4013
                [†]

                These authors contributed equally to this work.

                [‡]

                Current address: The Princess Grace Hospital, 42-52 Nottingham Place, London W1U 5NY, UK.

                [§]

                Current address: Singapore-MIT Alliance for Research and Technology, 1 CREATE Way, Singapore 138602, Singapore.

                Author information
                https://orcid.org/0000-0001-6852-4570
                https://orcid.org/0000-0003-2723-2023
                Article
                ijms-21-03515
                10.3390/ijms21103515
                7278942
                32429215
                30044345-0d1f-4dba-9dcd-10cb12a9f992
                © 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
                : 20 April 2020
                : 10 May 2020
                Categories
                Article

                Molecular biology
                endometriosis,cytokines,peritoneal fluid,microenvironment,precision medicine
                Molecular biology
                endometriosis, cytokines, peritoneal fluid, microenvironment, precision medicine

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