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E 2 -mediated EMT by activation of β-catenin/Snail signalling during the development of ovarian endometriosis
Endometriosis is an oestrogen-dependent disease, and epithelial-mesenchymal transition (EMT) is involved in the process of endometriosis. Whether oestrogen could induce EMT in endometriosis remains largely unknown. Here, we reported that up-regulated expression of EMT markers in ovarian chocolate cy...
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Published in: | Journal of cellular and molecular medicine 2019-12, Vol.23 (12), p.8035-8045 |
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creator | Xiong, Wenqian Zhang, Ling Liu, Hengwei Li, Na Du, Yu He, Haitang Zhang, Zhibing Liu, Yi |
description | Endometriosis is an oestrogen-dependent disease, and epithelial-mesenchymal transition (EMT) is involved in the process of endometriosis. Whether oestrogen could induce EMT in endometriosis remains largely unknown. Here, we reported that up-regulated expression of EMT markers in ovarian chocolate cyst is accompanied by high expression 17β-hydroxysteroid dehydrogenase 1 (17β-HSD1), and exposure of primary human endometrial epithelial cells to oestradiol conditions could promote EMT occurrence and activate both β-catenin and Snail signalling. Furthermore, we found nuclear β-catenin and Snail expression was closely linked in ovarian endometriosis, and β-catenin knockdown abrogated oestrogen-induced Snail mediated EMT in vitro. This is due to that β-catenin/ TCF-3 could bind to Snail promoter and activate its transcription. These results suggested that β-catenin signalling functions as the Snail activator and plays a critical role in oestradiol-induced EMT in endometriosis. |
doi_str_mv | 10.1111/jcmm.14668 |
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Whether oestrogen could induce EMT in endometriosis remains largely unknown. Here, we reported that up-regulated expression of EMT markers in ovarian chocolate cyst is accompanied by high expression 17β-hydroxysteroid dehydrogenase 1 (17β-HSD1), and exposure of primary human endometrial epithelial cells to oestradiol conditions could promote EMT occurrence and activate both β-catenin and Snail signalling. Furthermore, we found nuclear β-catenin and Snail expression was closely linked in ovarian endometriosis, and β-catenin knockdown abrogated oestrogen-induced Snail mediated EMT in vitro. This is due to that β-catenin/ TCF-3 could bind to Snail promoter and activate its transcription. These results suggested that β-catenin signalling functions as the Snail activator and plays a critical role in oestradiol-induced EMT in endometriosis.</description><identifier>ISSN: 1582-1838</identifier><identifier>EISSN: 1582-4934</identifier><identifier>DOI: 10.1111/jcmm.14668</identifier><identifier>PMID: 31560827</identifier><language>eng</language><publisher>England: John Wiley & Sons, Inc</publisher><subject>17-Hydroxysteroid Dehydrogenases - metabolism ; Adult ; beta Catenin - metabolism ; Cadherins - metabolism ; Catenin ; Cell Movement - drug effects ; Cells, Cultured ; Chocolate ; Chromatin Immunoprecipitation ; Cysts ; Endometriosis ; Endometriosis - etiology ; Endometriosis - metabolism ; Endometrium ; Endometrium - cytology ; Endometrium - drug effects ; Endometrium - metabolism ; Epithelial cells ; Epithelial Cells - drug effects ; Epithelial Cells - metabolism ; Epithelial-Mesenchymal Transition - drug effects ; Estradiol - pharmacology ; Estradiol - physiology ; Estrogens ; Estrogens - pharmacology ; Female ; Gynecology ; Humans ; Infertility ; Menstruation ; Mesenchyme ; Obstetrics ; Ovarian cancer ; Ovarian Cysts - metabolism ; Pathogenesis ; Receptors, Estrogen - antagonists & inhibitors ; Reproductive health ; RNA, Small Interfering ; Signal Transduction - drug effects ; Snail Family Transcription Factors - metabolism ; Transcription ; Transcription factors ; Up-Regulation ; Womens health</subject><ispartof>Journal of cellular and molecular medicine, 2019-12, Vol.23 (12), p.8035-8045</ispartof><rights>2019 The Authors. Journal of Cellular and Molecular Medicine published by John Wiley & Sons Ltd and Foundation for Cellular and Molecular Medicine.</rights><rights>2019. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c212t-38788234bc483fe298e14b0a1d426043180eddd4ee3f994b8da0bbf7163a48bc3</citedby><cites>FETCH-LOGICAL-c212t-38788234bc483fe298e14b0a1d426043180eddd4ee3f994b8da0bbf7163a48bc3</cites><orcidid>0000-0002-7136-9265 ; 0000-0002-5753-8704</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2313794867/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2313794867?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,25753,27924,27925,37012,44590,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31560827$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Xiong, Wenqian</creatorcontrib><creatorcontrib>Zhang, Ling</creatorcontrib><creatorcontrib>Liu, Hengwei</creatorcontrib><creatorcontrib>Li, Na</creatorcontrib><creatorcontrib>Du, Yu</creatorcontrib><creatorcontrib>He, Haitang</creatorcontrib><creatorcontrib>Zhang, Zhibing</creatorcontrib><creatorcontrib>Liu, Yi</creatorcontrib><title>E 2 -mediated EMT by activation of β-catenin/Snail signalling during the development of ovarian endometriosis</title><title>Journal of cellular and molecular medicine</title><addtitle>J Cell Mol Med</addtitle><description>Endometriosis is an oestrogen-dependent disease, and epithelial-mesenchymal transition (EMT) is involved in the process of endometriosis. Whether oestrogen could induce EMT in endometriosis remains largely unknown. Here, we reported that up-regulated expression of EMT markers in ovarian chocolate cyst is accompanied by high expression 17β-hydroxysteroid dehydrogenase 1 (17β-HSD1), and exposure of primary human endometrial epithelial cells to oestradiol conditions could promote EMT occurrence and activate both β-catenin and Snail signalling. Furthermore, we found nuclear β-catenin and Snail expression was closely linked in ovarian endometriosis, and β-catenin knockdown abrogated oestrogen-induced Snail mediated EMT in vitro. This is due to that β-catenin/ TCF-3 could bind to Snail promoter and activate its transcription. These results suggested that β-catenin signalling functions as the Snail activator and plays a critical role in oestradiol-induced EMT in endometriosis.</description><subject>17-Hydroxysteroid Dehydrogenases - metabolism</subject><subject>Adult</subject><subject>beta Catenin - metabolism</subject><subject>Cadherins - metabolism</subject><subject>Catenin</subject><subject>Cell Movement - drug effects</subject><subject>Cells, Cultured</subject><subject>Chocolate</subject><subject>Chromatin Immunoprecipitation</subject><subject>Cysts</subject><subject>Endometriosis</subject><subject>Endometriosis - etiology</subject><subject>Endometriosis - metabolism</subject><subject>Endometrium</subject><subject>Endometrium - cytology</subject><subject>Endometrium - drug effects</subject><subject>Endometrium - metabolism</subject><subject>Epithelial cells</subject><subject>Epithelial Cells - drug effects</subject><subject>Epithelial Cells - metabolism</subject><subject>Epithelial-Mesenchymal Transition - drug effects</subject><subject>Estradiol - pharmacology</subject><subject>Estradiol - physiology</subject><subject>Estrogens</subject><subject>Estrogens - pharmacology</subject><subject>Female</subject><subject>Gynecology</subject><subject>Humans</subject><subject>Infertility</subject><subject>Menstruation</subject><subject>Mesenchyme</subject><subject>Obstetrics</subject><subject>Ovarian cancer</subject><subject>Ovarian Cysts - metabolism</subject><subject>Pathogenesis</subject><subject>Receptors, Estrogen - antagonists & inhibitors</subject><subject>Reproductive health</subject><subject>RNA, Small Interfering</subject><subject>Signal Transduction - drug effects</subject><subject>Snail Family Transcription Factors - metabolism</subject><subject>Transcription</subject><subject>Transcription factors</subject><subject>Up-Regulation</subject><subject>Womens health</subject><issn>1582-1838</issn><issn>1582-4934</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNo9kEtOwzAQhi0EoqWw4QDIEjuktH41cZaoKg-piAVlHTnxpLhK7GK7lXotDsKZSGhhNv9I881o9CF0TcmYdjVZV207piJN5Qka0qlkici5OD32VHI5QBchrAnhKeX5ORpwOk2JZNkQ2TlmOGlBGxVB4_nLEpd7rKpodioaZ7Gr8fdXUnVTa-zkzSrT4GBWVjWNsSust76P-AFYww4at2nBxn7L7ZQ3ymKw2rUQvXHBhEt0VqsmwNUxR-j9Yb6cPSWL18fn2f0iqRhlMeEyk5JxUVZC8hpYLoGKkiiqBUuJ4FQS0FoLAF7nuSilVqQs64ymXAlZVnyEbg93N959biHEYu22vns6FIxTnuVCpllH3R2oyrsQPNTFxptW-X1BSdGrLXq1xa_aDr45ntyWna9_9M8l_wHEv3Vm</recordid><startdate>201912</startdate><enddate>201912</enddate><creator>Xiong, Wenqian</creator><creator>Zhang, Ling</creator><creator>Liu, Hengwei</creator><creator>Li, Na</creator><creator>Du, Yu</creator><creator>He, Haitang</creator><creator>Zhang, Zhibing</creator><creator>Liu, Yi</creator><general>John Wiley & Sons, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>RC3</scope><orcidid>https://orcid.org/0000-0002-7136-9265</orcidid><orcidid>https://orcid.org/0000-0002-5753-8704</orcidid></search><sort><creationdate>201912</creationdate><title>E 2 -mediated EMT by activation of β-catenin/Snail signalling during the development of ovarian endometriosis</title><author>Xiong, Wenqian ; Zhang, Ling ; Liu, Hengwei ; Li, Na ; Du, Yu ; He, Haitang ; Zhang, Zhibing ; Liu, Yi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c212t-38788234bc483fe298e14b0a1d426043180eddd4ee3f994b8da0bbf7163a48bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>17-Hydroxysteroid Dehydrogenases - 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Whether oestrogen could induce EMT in endometriosis remains largely unknown. Here, we reported that up-regulated expression of EMT markers in ovarian chocolate cyst is accompanied by high expression 17β-hydroxysteroid dehydrogenase 1 (17β-HSD1), and exposure of primary human endometrial epithelial cells to oestradiol conditions could promote EMT occurrence and activate both β-catenin and Snail signalling. Furthermore, we found nuclear β-catenin and Snail expression was closely linked in ovarian endometriosis, and β-catenin knockdown abrogated oestrogen-induced Snail mediated EMT in vitro. This is due to that β-catenin/ TCF-3 could bind to Snail promoter and activate its transcription. 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subjects | 17-Hydroxysteroid Dehydrogenases - metabolism Adult beta Catenin - metabolism Cadherins - metabolism Catenin Cell Movement - drug effects Cells, Cultured Chocolate Chromatin Immunoprecipitation Cysts Endometriosis Endometriosis - etiology Endometriosis - metabolism Endometrium Endometrium - cytology Endometrium - drug effects Endometrium - metabolism Epithelial cells Epithelial Cells - drug effects Epithelial Cells - metabolism Epithelial-Mesenchymal Transition - drug effects Estradiol - pharmacology Estradiol - physiology Estrogens Estrogens - pharmacology Female Gynecology Humans Infertility Menstruation Mesenchyme Obstetrics Ovarian cancer Ovarian Cysts - metabolism Pathogenesis Receptors, Estrogen - antagonists & inhibitors Reproductive health RNA, Small Interfering Signal Transduction - drug effects Snail Family Transcription Factors - metabolism Transcription Transcription factors Up-Regulation Womens health |
title | E 2 -mediated EMT by activation of β-catenin/Snail signalling during the development of ovarian endometriosis |
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