Defective endometrial prostaglandin synthesis identified in patients with repeated implantation failure undergoing in vitro fertilization

Objective To define the role of prostaglandins (PG) in the endometrium of patients with repeated failure of embryo implantation. Prostaglandins are produced after the sequential oxidation of arachidonic acid by cyclooxygenases (COX-1 and COX-2) and terminal PG synthases. Design Case-control study. S...

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Veröffentlicht in:Fertility and sterility 2010-09, Vol.94 (4), p.1271-1278
Hauptverfasser: Achache, Hanna, M.Sc, Tsafrir, Avi, M.D, Prus, Diana, M.D, Reich, Reuven, Ph.D, Revel, Ariel, M.D
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container_end_page 1278
container_issue 4
container_start_page 1271
container_title Fertility and sterility
container_volume 94
creator Achache, Hanna, M.Sc
Tsafrir, Avi, M.D
Prus, Diana, M.D
Reich, Reuven, Ph.D
Revel, Ariel, M.D
description Objective To define the role of prostaglandins (PG) in the endometrium of patients with repeated failure of embryo implantation. Prostaglandins are produced after the sequential oxidation of arachidonic acid by cyclooxygenases (COX-1 and COX-2) and terminal PG synthases. Design Case-control study. Setting In vitro fertilization unit at a university hospital. Patient(s) Thirty-four women, comprising of 19 patients with repeated IVF failure and 15 controls with proven fertility. Intervention(s) Endometrial expression levels of the enzymes responsible for the PG synthesis were compared between the two groups. Main Outcome Measure(s) Cytosolic phospholipase A2 (cPLA2α ) expression and activity were assessed by Western blot. Expression of cyclooxygenase-2, secretory phospholipase A2 group IIA, V, and IB (sPLA2 -IIA, sPLA2 -V, sPLA2 -IB), glypican-1, PG E synthase, PG E receptors, and lysophosphatidic acid receptor 3 (LPA3) was measured by real-time polymerase chain reaction (PCR). Localization of COX-2, sPLA2 -IIA, and LPA3 within the secretory endometrium was detected by immunohistochemistry. Result(s) Patients displaying recurrent implantation failure expressed reduced levels of cPLA2α and COX-2 compared with controls. In response to this deficiency, sPLA2 -IIA was found to be overexpressed. Interestingly, LPA3, which is known to converge on the cPLA2 -arachidonic acid-COX-PG signaling pathway, was also decreased in these patients. Conclusion(s) Prostaglandin synthesis appears to be disrupted in patients with repeated IVF failure compared with fertile controls. We therefore suggest that reduced PG synthesis in the human endometrium may lead to poor endometrial receptivity.
doi_str_mv 10.1016/j.fertnstert.2009.07.1668
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Prostaglandins are produced after the sequential oxidation of arachidonic acid by cyclooxygenases (COX-1 and COX-2) and terminal PG synthases. Design Case-control study. Setting In vitro fertilization unit at a university hospital. Patient(s) Thirty-four women, comprising of 19 patients with repeated IVF failure and 15 controls with proven fertility. Intervention(s) Endometrial expression levels of the enzymes responsible for the PG synthesis were compared between the two groups. Main Outcome Measure(s) Cytosolic phospholipase A2 (cPLA2α ) expression and activity were assessed by Western blot. Expression of cyclooxygenase-2, secretory phospholipase A2 group IIA, V, and IB (sPLA2 -IIA, sPLA2 -V, sPLA2 -IB), glypican-1, PG E synthase, PG E receptors, and lysophosphatidic acid receptor 3 (LPA3) was measured by real-time polymerase chain reaction (PCR). Localization of COX-2, sPLA2 -IIA, and LPA3 within the secretory endometrium was detected by immunohistochemistry. Result(s) Patients displaying recurrent implantation failure expressed reduced levels of cPLA2α and COX-2 compared with controls. In response to this deficiency, sPLA2 -IIA was found to be overexpressed. Interestingly, LPA3, which is known to converge on the cPLA2 -arachidonic acid-COX-PG signaling pathway, was also decreased in these patients. Conclusion(s) Prostaglandin synthesis appears to be disrupted in patients with repeated IVF failure compared with fertile controls. We therefore suggest that reduced PG synthesis in the human endometrium may lead to poor endometrial receptivity.</description><identifier>ISSN: 0015-0282</identifier><identifier>EISSN: 1556-5653</identifier><identifier>DOI: 10.1016/j.fertnstert.2009.07.1668</identifier><identifier>PMID: 19815191</identifier><identifier>CODEN: FESTAS</identifier><language>eng</language><publisher>New York, NY: Elsevier Inc</publisher><subject>Abortion, Habitual - diagnosis ; Abortion, Habitual - etiology ; Abortion, Habitual - genetics ; Abortion, Habitual - metabolism ; Adult ; Biological and medical sciences ; Birth control ; Case-Control Studies ; Cyclooxygenase 2 - genetics ; Cyclooxygenase 2 - metabolism ; Embryo Implantation - genetics ; Embryo Implantation - physiology ; Embryo Loss - diagnosis ; Embryo Loss - etiology ; Embryo Loss - genetics ; Embryo Loss - metabolism ; endometrial receptivity ; Endometrium ; Endometrium - metabolism ; Endometrium - pathology ; Female ; Fertility - genetics ; Fertility - physiology ; Fertilization in Vitro ; Group IV Phospholipases A2 - genetics ; Group IV Phospholipases A2 - metabolism ; Gynecology. Andrology. Obstetrics ; Humans ; in vitro fertilization ; Internal Medicine ; Lipid Metabolism Disorders - complications ; Lipid Metabolism Disorders - diagnosis ; Lipid Metabolism Disorders - genetics ; Lipid Metabolism Disorders - metabolism ; Male ; Medical sciences ; Obstetrics and Gynecology ; Phospholipases A2, Secretory - genetics ; Phospholipases A2, Secretory - metabolism ; prostaglandins ; Prostaglandins - biosynthesis ; Receptors, Prostaglandin E - genetics ; Receptors, Prostaglandin E - metabolism ; repeated implantation failure ; Sterility. Assisted procreation ; window of implantation ; Young Adult</subject><ispartof>Fertility and sterility, 2010-09, Vol.94 (4), p.1271-1278</ispartof><rights>American Society for Reproductive Medicine</rights><rights>2010 American Society for Reproductive Medicine</rights><rights>2015 INIST-CNRS</rights><rights>Copyright (c) 2010 American Society for Reproductive Medicine. Published by Elsevier Inc. 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Prostaglandins are produced after the sequential oxidation of arachidonic acid by cyclooxygenases (COX-1 and COX-2) and terminal PG synthases. Design Case-control study. Setting In vitro fertilization unit at a university hospital. Patient(s) Thirty-four women, comprising of 19 patients with repeated IVF failure and 15 controls with proven fertility. Intervention(s) Endometrial expression levels of the enzymes responsible for the PG synthesis were compared between the two groups. Main Outcome Measure(s) Cytosolic phospholipase A2 (cPLA2α ) expression and activity were assessed by Western blot. Expression of cyclooxygenase-2, secretory phospholipase A2 group IIA, V, and IB (sPLA2 -IIA, sPLA2 -V, sPLA2 -IB), glypican-1, PG E synthase, PG E receptors, and lysophosphatidic acid receptor 3 (LPA3) was measured by real-time polymerase chain reaction (PCR). Localization of COX-2, sPLA2 -IIA, and LPA3 within the secretory endometrium was detected by immunohistochemistry. Result(s) Patients displaying recurrent implantation failure expressed reduced levels of cPLA2α and COX-2 compared with controls. In response to this deficiency, sPLA2 -IIA was found to be overexpressed. Interestingly, LPA3, which is known to converge on the cPLA2 -arachidonic acid-COX-PG signaling pathway, was also decreased in these patients. Conclusion(s) Prostaglandin synthesis appears to be disrupted in patients with repeated IVF failure compared with fertile controls. We therefore suggest that reduced PG synthesis in the human endometrium may lead to poor endometrial receptivity.</description><subject>Abortion, Habitual - diagnosis</subject><subject>Abortion, Habitual - etiology</subject><subject>Abortion, Habitual - genetics</subject><subject>Abortion, Habitual - metabolism</subject><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Birth control</subject><subject>Case-Control Studies</subject><subject>Cyclooxygenase 2 - genetics</subject><subject>Cyclooxygenase 2 - metabolism</subject><subject>Embryo Implantation - genetics</subject><subject>Embryo Implantation - physiology</subject><subject>Embryo Loss - diagnosis</subject><subject>Embryo Loss - etiology</subject><subject>Embryo Loss - genetics</subject><subject>Embryo Loss - metabolism</subject><subject>endometrial receptivity</subject><subject>Endometrium</subject><subject>Endometrium - metabolism</subject><subject>Endometrium - pathology</subject><subject>Female</subject><subject>Fertility - genetics</subject><subject>Fertility - physiology</subject><subject>Fertilization in Vitro</subject><subject>Group IV Phospholipases A2 - genetics</subject><subject>Group IV Phospholipases A2 - metabolism</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Humans</subject><subject>in vitro fertilization</subject><subject>Internal Medicine</subject><subject>Lipid Metabolism Disorders - complications</subject><subject>Lipid Metabolism Disorders - diagnosis</subject><subject>Lipid Metabolism Disorders - genetics</subject><subject>Lipid Metabolism Disorders - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Obstetrics and Gynecology</subject><subject>Phospholipases A2, Secretory - genetics</subject><subject>Phospholipases A2, Secretory - metabolism</subject><subject>prostaglandins</subject><subject>Prostaglandins - biosynthesis</subject><subject>Receptors, Prostaglandin E - genetics</subject><subject>Receptors, Prostaglandin E - metabolism</subject><subject>repeated implantation failure</subject><subject>Sterility. Assisted procreation</subject><subject>window of implantation</subject><subject>Young Adult</subject><issn>0015-0282</issn><issn>1556-5653</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNUk2v1CAUbYzGNz79C6YujKtWKNCWjYkZP5OXuFDXhMJl3h07tAIdM_4D_7XUmfgSV4YEAvec-3EORfGMkpoS2r7c1w5C8jHlvW4IkTXpatq2_b1iQ4VoK9EKdr_YEEJFRZq-uSoexbgnhLS0ax4WV1T2VFBJN8WvN-DAJDxCCd5OB0gB9VjOYYpJ70btLfoynny6hYixRAs-oUOwZX6fdcJ8j-UPTLdlgBl0WiOHORNTDk6-dBrHJUC5eAthN6HfrcwjpjCV6xQ44s8_yMfFA6fHCE8u53Xx9d3bL9sP1c2n9x-3r28qI2iTKsop9KznGrixTFMY8uJDxwbCNTEgzOBAdEzrXrTOStcMjPKh77noJeecXRcvznnzjN8XiEkdMBoYc8swLVF1gknZtV2bkfKMNFmNGMCpOeBBh5OiRK1GqL26M0KtRijSqdWIzH16qbIMB7B3zIvyGfD8AtDR6NEF7Q3Gv7iGUZmha7vbMw6yJkeEoKLJohuwGLJxyk74X-28-ieLGdFjLvwNThD30xJ8Fl1RFRtF1Of156wfh0jCuMjt_ga2mMbU</recordid><startdate>20100901</startdate><enddate>20100901</enddate><creator>Achache, Hanna, M.Sc</creator><creator>Tsafrir, Avi, M.D</creator><creator>Prus, Diana, M.D</creator><creator>Reich, Reuven, Ph.D</creator><creator>Revel, Ariel, M.D</creator><general>Elsevier Inc</general><general>Elsevier</general><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>20100901</creationdate><title>Defective endometrial prostaglandin synthesis identified in patients with repeated implantation failure undergoing in vitro fertilization</title><author>Achache, Hanna, M.Sc ; Tsafrir, Avi, M.D ; Prus, Diana, M.D ; Reich, Reuven, Ph.D ; Revel, Ariel, M.D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c512t-141e8384ae4cd3a1ebebe4b73b04a0ce5cbfe573aa856fd9f2b314b8845894443</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Abortion, Habitual - diagnosis</topic><topic>Abortion, Habitual - etiology</topic><topic>Abortion, Habitual - genetics</topic><topic>Abortion, Habitual - metabolism</topic><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Birth control</topic><topic>Case-Control Studies</topic><topic>Cyclooxygenase 2 - genetics</topic><topic>Cyclooxygenase 2 - metabolism</topic><topic>Embryo Implantation - genetics</topic><topic>Embryo Implantation - physiology</topic><topic>Embryo Loss - diagnosis</topic><topic>Embryo Loss - etiology</topic><topic>Embryo Loss - genetics</topic><topic>Embryo Loss - metabolism</topic><topic>endometrial receptivity</topic><topic>Endometrium</topic><topic>Endometrium - metabolism</topic><topic>Endometrium - pathology</topic><topic>Female</topic><topic>Fertility - genetics</topic><topic>Fertility - physiology</topic><topic>Fertilization in Vitro</topic><topic>Group IV Phospholipases A2 - genetics</topic><topic>Group IV Phospholipases A2 - metabolism</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Humans</topic><topic>in vitro fertilization</topic><topic>Internal Medicine</topic><topic>Lipid Metabolism Disorders - complications</topic><topic>Lipid Metabolism Disorders - diagnosis</topic><topic>Lipid Metabolism Disorders - genetics</topic><topic>Lipid Metabolism Disorders - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Obstetrics and Gynecology</topic><topic>Phospholipases A2, Secretory - genetics</topic><topic>Phospholipases A2, Secretory - metabolism</topic><topic>prostaglandins</topic><topic>Prostaglandins - biosynthesis</topic><topic>Receptors, Prostaglandin E - genetics</topic><topic>Receptors, Prostaglandin E - metabolism</topic><topic>repeated implantation failure</topic><topic>Sterility. Assisted procreation</topic><topic>window of implantation</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Achache, Hanna, M.Sc</creatorcontrib><creatorcontrib>Tsafrir, Avi, M.D</creatorcontrib><creatorcontrib>Prus, Diana, M.D</creatorcontrib><creatorcontrib>Reich, Reuven, Ph.D</creatorcontrib><creatorcontrib>Revel, Ariel, M.D</creatorcontrib><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>Fertility and sterility</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Achache, Hanna, M.Sc</au><au>Tsafrir, Avi, M.D</au><au>Prus, Diana, M.D</au><au>Reich, Reuven, Ph.D</au><au>Revel, Ariel, M.D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Defective endometrial prostaglandin synthesis identified in patients with repeated implantation failure undergoing in vitro fertilization</atitle><jtitle>Fertility and sterility</jtitle><addtitle>Fertil Steril</addtitle><date>2010-09-01</date><risdate>2010</risdate><volume>94</volume><issue>4</issue><spage>1271</spage><epage>1278</epage><pages>1271-1278</pages><issn>0015-0282</issn><eissn>1556-5653</eissn><coden>FESTAS</coden><abstract>Objective To define the role of prostaglandins (PG) in the endometrium of patients with repeated failure of embryo implantation. Prostaglandins are produced after the sequential oxidation of arachidonic acid by cyclooxygenases (COX-1 and COX-2) and terminal PG synthases. Design Case-control study. Setting In vitro fertilization unit at a university hospital. Patient(s) Thirty-four women, comprising of 19 patients with repeated IVF failure and 15 controls with proven fertility. Intervention(s) Endometrial expression levels of the enzymes responsible for the PG synthesis were compared between the two groups. Main Outcome Measure(s) Cytosolic phospholipase A2 (cPLA2α ) expression and activity were assessed by Western blot. Expression of cyclooxygenase-2, secretory phospholipase A2 group IIA, V, and IB (sPLA2 -IIA, sPLA2 -V, sPLA2 -IB), glypican-1, PG E synthase, PG E receptors, and lysophosphatidic acid receptor 3 (LPA3) was measured by real-time polymerase chain reaction (PCR). Localization of COX-2, sPLA2 -IIA, and LPA3 within the secretory endometrium was detected by immunohistochemistry. Result(s) Patients displaying recurrent implantation failure expressed reduced levels of cPLA2α and COX-2 compared with controls. In response to this deficiency, sPLA2 -IIA was found to be overexpressed. Interestingly, LPA3, which is known to converge on the cPLA2 -arachidonic acid-COX-PG signaling pathway, was also decreased in these patients. Conclusion(s) Prostaglandin synthesis appears to be disrupted in patients with repeated IVF failure compared with fertile controls. We therefore suggest that reduced PG synthesis in the human endometrium may lead to poor endometrial receptivity.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>19815191</pmid><doi>10.1016/j.fertnstert.2009.07.1668</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record>
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subjects Abortion, Habitual - diagnosis
Abortion, Habitual - etiology
Abortion, Habitual - genetics
Abortion, Habitual - metabolism
Adult
Biological and medical sciences
Birth control
Case-Control Studies
Cyclooxygenase 2 - genetics
Cyclooxygenase 2 - metabolism
Embryo Implantation - genetics
Embryo Implantation - physiology
Embryo Loss - diagnosis
Embryo Loss - etiology
Embryo Loss - genetics
Embryo Loss - metabolism
endometrial receptivity
Endometrium
Endometrium - metabolism
Endometrium - pathology
Female
Fertility - genetics
Fertility - physiology
Fertilization in Vitro
Group IV Phospholipases A2 - genetics
Group IV Phospholipases A2 - metabolism
Gynecology. Andrology. Obstetrics
Humans
in vitro fertilization
Internal Medicine
Lipid Metabolism Disorders - complications
Lipid Metabolism Disorders - diagnosis
Lipid Metabolism Disorders - genetics
Lipid Metabolism Disorders - metabolism
Male
Medical sciences
Obstetrics and Gynecology
Phospholipases A2, Secretory - genetics
Phospholipases A2, Secretory - metabolism
prostaglandins
Prostaglandins - biosynthesis
Receptors, Prostaglandin E - genetics
Receptors, Prostaglandin E - metabolism
repeated implantation failure
Sterility. Assisted procreation
window of implantation
Young Adult
title Defective endometrial prostaglandin synthesis identified in patients with repeated implantation failure undergoing in vitro fertilization
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