Effects of the levonorgestrel-releasing intrauterine system on cell proliferation, Fas expression and steroid receptors in endometriosis lesions and normal endometrium
BACKGROUND The objectives of this study were: (i) to evaluate the effects of the levonorgestrel-releasing intrauterine system (LNG-IUS) on both proliferation and apoptosis markers and hormone receptors of the eutopic and ectopic endometrium of women experiencing pain related to endometriosis and (ii...
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Veröffentlicht in: | Human reproduction (Oxford) 2009-11, Vol.24 (11), p.2736-2745 |
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creator | Gomes, M.K.O. Rosa-e-Silva, J.C. Garcia, S.B. de Sá Rosa-e-Silva, A.C. Japur Turatti, A. Vieira, C.S. Ferriani, R.A. |
description | BACKGROUND The objectives of this study were: (i) to evaluate the effects of the levonorgestrel-releasing intrauterine system (LNG-IUS) on both proliferation and apoptosis markers and hormone receptors of the eutopic and ectopic endometrium of women experiencing pain related to endometriosis and (ii) to compare the results with those obtained with GnRH agonist (GnRHa) injections. METHODS Pre- and post-treatment endometrium and endometriosis specimens were obtained from 22 women experiencing pain related to endometriosis who were treated with LNG-IUS (n = 11) or GnRHa (n = 11) for 6 months. Changes in the expression of proliferating cell nuclear antigen, Fas, progesterone receptor (PRA) and estrogen receptor α (ER-α) were analyzed by immunohistochemistry. RESULTS The cell proliferation index was significantly reduced in the epithelium and stroma of both the eutopic and the ectopic endometrium after treatment with the LNG-IUS and GnRHa. Only LNG-IUS users showed an increased H-score for Fas in the epithelium of the eutopic and ectopic endometrium (P < 0.05). Expression of ER-α and PRA by the glandular epithelium was lower in the eutopic endometrium after both treatments, but this reduction was noted in the ectopic endometrium only after LNG-IUS treatments (P < 0.05). No difference was detected between groups for any of the markers. CONCLUSIONS LNG-IUS reduced both cell proliferation and the expression of PRA and ER-α and increased Fas expression in the eutopic and ectopic endometrium of patients with endometriosis. Some of these actions were not observed with GnRHa. |
doi_str_mv | 10.1093/humrep/dep288 |
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Japur ; Turatti, A. ; Vieira, C.S. ; Ferriani, R.A.</creator><creatorcontrib>Gomes, M.K.O. ; Rosa-e-Silva, J.C. ; Garcia, S.B. ; de Sá Rosa-e-Silva, A.C. Japur ; Turatti, A. ; Vieira, C.S. ; Ferriani, R.A.</creatorcontrib><description>BACKGROUND The objectives of this study were: (i) to evaluate the effects of the levonorgestrel-releasing intrauterine system (LNG-IUS) on both proliferation and apoptosis markers and hormone receptors of the eutopic and ectopic endometrium of women experiencing pain related to endometriosis and (ii) to compare the results with those obtained with GnRH agonist (GnRHa) injections. METHODS Pre- and post-treatment endometrium and endometriosis specimens were obtained from 22 women experiencing pain related to endometriosis who were treated with LNG-IUS (n = 11) or GnRHa (n = 11) for 6 months. Changes in the expression of proliferating cell nuclear antigen, Fas, progesterone receptor (PRA) and estrogen receptor α (ER-α) were analyzed by immunohistochemistry. RESULTS The cell proliferation index was significantly reduced in the epithelium and stroma of both the eutopic and the ectopic endometrium after treatment with the LNG-IUS and GnRHa. Only LNG-IUS users showed an increased H-score for Fas in the epithelium of the eutopic and ectopic endometrium (P < 0.05). Expression of ER-α and PRA by the glandular epithelium was lower in the eutopic endometrium after both treatments, but this reduction was noted in the ectopic endometrium only after LNG-IUS treatments (P < 0.05). No difference was detected between groups for any of the markers. CONCLUSIONS LNG-IUS reduced both cell proliferation and the expression of PRA and ER-α and increased Fas expression in the eutopic and ectopic endometrium of patients with endometriosis. Some of these actions were not observed with GnRHa.</description><identifier>ISSN: 0268-1161</identifier><identifier>EISSN: 1460-2350</identifier><identifier>DOI: 10.1093/humrep/dep288</identifier><identifier>PMID: 19661125</identifier><identifier>CODEN: HUREEE</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adolescent ; Adult ; apoptosis ; Apoptosis - drug effects ; Biological and medical sciences ; Cell Proliferation - drug effects ; endometriosis ; Endometriosis - complications ; Endometriosis - metabolism ; Endometriosis - pathology ; Endometrium - drug effects ; Endometrium - metabolism ; Endometrium - pathology ; Estrogen Receptor alpha - metabolism ; fas Receptor - metabolism ; Female ; GnRH agonist ; Gonadotropin-Releasing Hormone - agonists ; Gynecology. Andrology. Obstetrics ; Humans ; Levonorgestrel - administration & dosage ; Levonorgestrel - pharmacology ; levonorgestrel-releasing intrauterine system ; Medical sciences ; Pain - etiology ; Receptors, Progesterone - metabolism ; steroid receptor</subject><ispartof>Human reproduction (Oxford), 2009-11, Vol.24 (11), p.2736-2745</ispartof><rights>The Author 2009. Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org 2009</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c498t-b1c1945014941d97ae0ddc324eeae70a3cba537fe6473601cc85618fd613aaf3</citedby><cites>FETCH-LOGICAL-c498t-b1c1945014941d97ae0ddc324eeae70a3cba537fe6473601cc85618fd613aaf3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1584,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22047121$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19661125$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gomes, M.K.O.</creatorcontrib><creatorcontrib>Rosa-e-Silva, J.C.</creatorcontrib><creatorcontrib>Garcia, S.B.</creatorcontrib><creatorcontrib>de Sá Rosa-e-Silva, A.C. Japur</creatorcontrib><creatorcontrib>Turatti, A.</creatorcontrib><creatorcontrib>Vieira, C.S.</creatorcontrib><creatorcontrib>Ferriani, R.A.</creatorcontrib><title>Effects of the levonorgestrel-releasing intrauterine system on cell proliferation, Fas expression and steroid receptors in endometriosis lesions and normal endometrium</title><title>Human reproduction (Oxford)</title><addtitle>Hum Reprod</addtitle><description>BACKGROUND The objectives of this study were: (i) to evaluate the effects of the levonorgestrel-releasing intrauterine system (LNG-IUS) on both proliferation and apoptosis markers and hormone receptors of the eutopic and ectopic endometrium of women experiencing pain related to endometriosis and (ii) to compare the results with those obtained with GnRH agonist (GnRHa) injections. METHODS Pre- and post-treatment endometrium and endometriosis specimens were obtained from 22 women experiencing pain related to endometriosis who were treated with LNG-IUS (n = 11) or GnRHa (n = 11) for 6 months. Changes in the expression of proliferating cell nuclear antigen, Fas, progesterone receptor (PRA) and estrogen receptor α (ER-α) were analyzed by immunohistochemistry. RESULTS The cell proliferation index was significantly reduced in the epithelium and stroma of both the eutopic and the ectopic endometrium after treatment with the LNG-IUS and GnRHa. Only LNG-IUS users showed an increased H-score for Fas in the epithelium of the eutopic and ectopic endometrium (P < 0.05). Expression of ER-α and PRA by the glandular epithelium was lower in the eutopic endometrium after both treatments, but this reduction was noted in the ectopic endometrium only after LNG-IUS treatments (P < 0.05). No difference was detected between groups for any of the markers. CONCLUSIONS LNG-IUS reduced both cell proliferation and the expression of PRA and ER-α and increased Fas expression in the eutopic and ectopic endometrium of patients with endometriosis. Some of these actions were not observed with GnRHa.</description><subject>Adolescent</subject><subject>Adult</subject><subject>apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Biological and medical sciences</subject><subject>Cell Proliferation - drug effects</subject><subject>endometriosis</subject><subject>Endometriosis - complications</subject><subject>Endometriosis - metabolism</subject><subject>Endometriosis - pathology</subject><subject>Endometrium - drug effects</subject><subject>Endometrium - metabolism</subject><subject>Endometrium - pathology</subject><subject>Estrogen Receptor alpha - metabolism</subject><subject>fas Receptor - metabolism</subject><subject>Female</subject><subject>GnRH agonist</subject><subject>Gonadotropin-Releasing Hormone - agonists</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>Levonorgestrel - administration & dosage</subject><subject>Levonorgestrel - pharmacology</subject><subject>levonorgestrel-releasing intrauterine system</subject><subject>Medical sciences</subject><subject>Pain - etiology</subject><subject>Receptors, Progesterone - metabolism</subject><subject>steroid receptor</subject><issn>0268-1161</issn><issn>1460-2350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0UuL1TAUAOAginMdXbqVbEQX1kmaNm2XcpmHcEWQwRE3ITc9mYm2Sc1JZeYX-TfNtWVm6SIkgY_zJOQlZ-8568TJzTxGmE56mMq2fUQ2vJKsKEXNHpMNK2VbcC75EXmG-IOx_GzlU3LEOyk5L-sN-XNqLZiENFiaboAO8Dv4EK8BU4ShyAc0On9NnU9Rzwmi80DxDhOMNHhqYBjoFMPgLESdXPDv6JlGCrdTBMT8p9r3NPMYXE8jGJhSiJjjUfB9GCFFF9BhznzQ-I_nCkY9PIB5fE6eWD0gvFjvY3J5dnq5vSh2n88_bj_sClN1bSr23PCuqhmvuor3XaOB9b0RZQWgoWFamL2uRWNBVo2QjBvT1nkmtpdcaG3FMXmzhM0t_ZrzENTo8NCj9hBmVI2oWMfrus6yWKSJATGCVVN0o453ijN12IxaNqOWzWT_ao0870foH_S6igxer0Cj0YON2huH964sWdXwkmf3dnFhnv6bc63R5fnf3mMdfyrZiKZWF9--q_rqfHv1afdFfRV_Ab8Hu9o</recordid><startdate>20091101</startdate><enddate>20091101</enddate><creator>Gomes, M.K.O.</creator><creator>Rosa-e-Silva, J.C.</creator><creator>Garcia, S.B.</creator><creator>de Sá Rosa-e-Silva, A.C. Japur</creator><creator>Turatti, A.</creator><creator>Vieira, C.S.</creator><creator>Ferriani, R.A.</creator><general>Oxford University Press</general><scope>BSCLL</scope><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>20091101</creationdate><title>Effects of the levonorgestrel-releasing intrauterine system on cell proliferation, Fas expression and steroid receptors in endometriosis lesions and normal endometrium</title><author>Gomes, M.K.O. ; Rosa-e-Silva, J.C. ; Garcia, S.B. ; de Sá Rosa-e-Silva, A.C. Japur ; Turatti, A. ; Vieira, C.S. ; Ferriani, R.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c498t-b1c1945014941d97ae0ddc324eeae70a3cba537fe6473601cc85618fd613aaf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Biological and medical sciences</topic><topic>Cell Proliferation - drug effects</topic><topic>endometriosis</topic><topic>Endometriosis - complications</topic><topic>Endometriosis - metabolism</topic><topic>Endometriosis - pathology</topic><topic>Endometrium - drug effects</topic><topic>Endometrium - metabolism</topic><topic>Endometrium - pathology</topic><topic>Estrogen Receptor alpha - metabolism</topic><topic>fas Receptor - metabolism</topic><topic>Female</topic><topic>GnRH agonist</topic><topic>Gonadotropin-Releasing Hormone - agonists</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>Levonorgestrel - administration & dosage</topic><topic>Levonorgestrel - pharmacology</topic><topic>levonorgestrel-releasing intrauterine system</topic><topic>Medical sciences</topic><topic>Pain - etiology</topic><topic>Receptors, Progesterone - metabolism</topic><topic>steroid receptor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gomes, M.K.O.</creatorcontrib><creatorcontrib>Rosa-e-Silva, J.C.</creatorcontrib><creatorcontrib>Garcia, S.B.</creatorcontrib><creatorcontrib>de Sá Rosa-e-Silva, A.C. Japur</creatorcontrib><creatorcontrib>Turatti, A.</creatorcontrib><creatorcontrib>Vieira, C.S.</creatorcontrib><creatorcontrib>Ferriani, R.A.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Human reproduction (Oxford)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gomes, M.K.O.</au><au>Rosa-e-Silva, J.C.</au><au>Garcia, S.B.</au><au>de Sá Rosa-e-Silva, A.C. Japur</au><au>Turatti, A.</au><au>Vieira, C.S.</au><au>Ferriani, R.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of the levonorgestrel-releasing intrauterine system on cell proliferation, Fas expression and steroid receptors in endometriosis lesions and normal endometrium</atitle><jtitle>Human reproduction (Oxford)</jtitle><addtitle>Hum Reprod</addtitle><date>2009-11-01</date><risdate>2009</risdate><volume>24</volume><issue>11</issue><spage>2736</spage><epage>2745</epage><pages>2736-2745</pages><issn>0268-1161</issn><eissn>1460-2350</eissn><coden>HUREEE</coden><abstract>BACKGROUND The objectives of this study were: (i) to evaluate the effects of the levonorgestrel-releasing intrauterine system (LNG-IUS) on both proliferation and apoptosis markers and hormone receptors of the eutopic and ectopic endometrium of women experiencing pain related to endometriosis and (ii) to compare the results with those obtained with GnRH agonist (GnRHa) injections. METHODS Pre- and post-treatment endometrium and endometriosis specimens were obtained from 22 women experiencing pain related to endometriosis who were treated with LNG-IUS (n = 11) or GnRHa (n = 11) for 6 months. Changes in the expression of proliferating cell nuclear antigen, Fas, progesterone receptor (PRA) and estrogen receptor α (ER-α) were analyzed by immunohistochemistry. RESULTS The cell proliferation index was significantly reduced in the epithelium and stroma of both the eutopic and the ectopic endometrium after treatment with the LNG-IUS and GnRHa. Only LNG-IUS users showed an increased H-score for Fas in the epithelium of the eutopic and ectopic endometrium (P < 0.05). Expression of ER-α and PRA by the glandular epithelium was lower in the eutopic endometrium after both treatments, but this reduction was noted in the ectopic endometrium only after LNG-IUS treatments (P < 0.05). No difference was detected between groups for any of the markers. CONCLUSIONS LNG-IUS reduced both cell proliferation and the expression of PRA and ER-α and increased Fas expression in the eutopic and ectopic endometrium of patients with endometriosis. Some of these actions were not observed with GnRHa.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>19661125</pmid><doi>10.1093/humrep/dep288</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult apoptosis Apoptosis - drug effects Biological and medical sciences Cell Proliferation - drug effects endometriosis Endometriosis - complications Endometriosis - metabolism Endometriosis - pathology Endometrium - drug effects Endometrium - metabolism Endometrium - pathology Estrogen Receptor alpha - metabolism fas Receptor - metabolism Female GnRH agonist Gonadotropin-Releasing Hormone - agonists Gynecology. Andrology. Obstetrics Humans Levonorgestrel - administration & dosage Levonorgestrel - pharmacology levonorgestrel-releasing intrauterine system Medical sciences Pain - etiology Receptors, Progesterone - metabolism steroid receptor |
title | Effects of the levonorgestrel-releasing intrauterine system on cell proliferation, Fas expression and steroid receptors in endometriosis lesions and normal endometrium |
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