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Decreased placental glypican expression is associated with human fetal growth restriction
Placental mediated fetal growth restriction (FGR) is a leading cause of perinatal morbidity and mortality. Heparan sulphate proteoglycans (HSPG) are highly expressed in placentae and regulate haemostasis. We hypothesise that altered expression of HSPGs, glypicans (GPC) may contribute to the developm...
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Published in: | Placenta (Eastbourne) 2019-01, Vol.76, p.6-9 |
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creator | Gunatillake, T. Chui, A. Fitzpatrick, E. Ignjatovic, V. Monagle, P. Whitelock, J. Zanten, D. Eijsink, J. Borg, A. Stevenson, J. Brennecke, S.P. Erwich, J.J.H.M. Said, J.M. Murthi, P. |
description | Placental mediated fetal growth restriction (FGR) is a leading cause of perinatal morbidity and mortality. Heparan sulphate proteoglycans (HSPG) are highly expressed in placentae and regulate haemostasis. We hypothesise that altered expression of HSPGs, glypicans (GPC) may contribute to the development of FGR and small-for-gestational-age (SGA). GPC expression was determined in first-trimester chorionic villous samples collected from women with later SGA pregnancies and in placentae from third-trimester FGR and gestation-matched uncomplicated pregnancies. The expression of both GPC1 and GPC3 were significantly reduced in first-trimester SGA as well as in the third-trimester FGR placentae compared to controls. This is the first study to report a relationship between altered placental GPC expression and subsequent development of SGA/FGR.
•Heparan sulphate proteoglycans are abundantly expressed in human placentae.•Placental glypican expression is reduced in third-trimester FGR samples.•Reduced glypican expression in first-trimester pregnancy may contribute to the development of FGR. |
doi_str_mv | 10.1016/j.placenta.2018.12.007 |
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•Heparan sulphate proteoglycans are abundantly expressed in human placentae.•Placental glypican expression is reduced in third-trimester FGR samples.•Reduced glypican expression in first-trimester pregnancy may contribute to the development of FGR.</description><identifier>ISSN: 0143-4004</identifier><identifier>EISSN: 1532-3102</identifier><identifier>DOI: 10.1016/j.placenta.2018.12.007</identifier><identifier>PMID: 30803713</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adult ; Case-Control Studies ; Female ; Fetal growth ; Fetal Growth Retardation - metabolism ; Glypican ; Glypicans - metabolism ; Heparan sulphate ; Humans ; Infant, Newborn ; Infant, Small for Gestational Age ; Placenta - metabolism ; Pregnancy ; Pregnancy Trimester, First - metabolism ; Pregnancy Trimester, Third - metabolism ; Proteoglycans ; Restriction</subject><ispartof>Placenta (Eastbourne), 2019-01, Vol.76, p.6-9</ispartof><rights>2018</rights><rights>Copyright © 2018. Published by Elsevier Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c416t-575b9a5dc9f14ca8eff62bc720b34fc003ad08412a9fc9c2d44b665fdac1d2ad3</citedby><cites>FETCH-LOGICAL-c416t-575b9a5dc9f14ca8eff62bc720b34fc003ad08412a9fc9c2d44b665fdac1d2ad3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30803713$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gunatillake, T.</creatorcontrib><creatorcontrib>Chui, A.</creatorcontrib><creatorcontrib>Fitzpatrick, E.</creatorcontrib><creatorcontrib>Ignjatovic, V.</creatorcontrib><creatorcontrib>Monagle, P.</creatorcontrib><creatorcontrib>Whitelock, J.</creatorcontrib><creatorcontrib>Zanten, D.</creatorcontrib><creatorcontrib>Eijsink, J.</creatorcontrib><creatorcontrib>Borg, A.</creatorcontrib><creatorcontrib>Stevenson, J.</creatorcontrib><creatorcontrib>Brennecke, S.P.</creatorcontrib><creatorcontrib>Erwich, J.J.H.M.</creatorcontrib><creatorcontrib>Said, J.M.</creatorcontrib><creatorcontrib>Murthi, P.</creatorcontrib><title>Decreased placental glypican expression is associated with human fetal growth restriction</title><title>Placenta (Eastbourne)</title><addtitle>Placenta</addtitle><description>Placental mediated fetal growth restriction (FGR) is a leading cause of perinatal morbidity and mortality. Heparan sulphate proteoglycans (HSPG) are highly expressed in placentae and regulate haemostasis. We hypothesise that altered expression of HSPGs, glypicans (GPC) may contribute to the development of FGR and small-for-gestational-age (SGA). GPC expression was determined in first-trimester chorionic villous samples collected from women with later SGA pregnancies and in placentae from third-trimester FGR and gestation-matched uncomplicated pregnancies. The expression of both GPC1 and GPC3 were significantly reduced in first-trimester SGA as well as in the third-trimester FGR placentae compared to controls. This is the first study to report a relationship between altered placental GPC expression and subsequent development of SGA/FGR.
•Heparan sulphate proteoglycans are abundantly expressed in human placentae.•Placental glypican expression is reduced in third-trimester FGR samples.•Reduced glypican expression in first-trimester pregnancy may contribute to the development of FGR.</description><subject>Adult</subject><subject>Case-Control Studies</subject><subject>Female</subject><subject>Fetal growth</subject><subject>Fetal Growth Retardation - metabolism</subject><subject>Glypican</subject><subject>Glypicans - metabolism</subject><subject>Heparan sulphate</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Infant, Small for Gestational Age</subject><subject>Placenta - metabolism</subject><subject>Pregnancy</subject><subject>Pregnancy Trimester, First - metabolism</subject><subject>Pregnancy Trimester, Third - metabolism</subject><subject>Proteoglycans</subject><subject>Restriction</subject><issn>0143-4004</issn><issn>1532-3102</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNqFkE1v1DAQhi0EotuWv1DlyCXpjO183UClfEiVeimHnixnPKZeZZNgZyn997hslyunkaznnXf8CHGBUCFgc7mtltEST6utJGBXoawA2ldig7WSpUKQr8UGUKtSA-gTcZrSFgB6jfKtOFHQgWpRbcT9J6bINrErjgvH4sf4tASyU8G_l8gphXkqQipsSjMFu2b2MawPxcN-lxnPfyNxfsxPmV5joDUnzsUbb8fE717mmfj--fru6mt5c_vl29XHm5I0NmtZt_XQ29pR71GT7dj7Rg7UShiU9gSgrIMun217Tz1Jp_XQNLV3ltBJ69SZeH_Yu8T55z73m11IxONoJ573yUjsGqxlX7cZbQ4oxTmlyN4sMexsfDII5lmr2ZqjBfOs1aA0WWsOXrx07Icdu3-xo8cMfDgAnH_6K3A0iQJPxC5EptW4Ofyv4w-JiY7O</recordid><startdate>20190115</startdate><enddate>20190115</enddate><creator>Gunatillake, T.</creator><creator>Chui, A.</creator><creator>Fitzpatrick, E.</creator><creator>Ignjatovic, V.</creator><creator>Monagle, P.</creator><creator>Whitelock, J.</creator><creator>Zanten, D.</creator><creator>Eijsink, J.</creator><creator>Borg, A.</creator><creator>Stevenson, J.</creator><creator>Brennecke, S.P.</creator><creator>Erwich, J.J.H.M.</creator><creator>Said, J.M.</creator><creator>Murthi, P.</creator><general>Elsevier Ltd</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>7X8</scope></search><sort><creationdate>20190115</creationdate><title>Decreased placental glypican expression is associated with human fetal growth restriction</title><author>Gunatillake, T. ; Chui, A. ; Fitzpatrick, E. ; Ignjatovic, V. ; Monagle, P. ; Whitelock, J. ; Zanten, D. ; Eijsink, J. ; Borg, A. ; Stevenson, J. ; Brennecke, S.P. ; Erwich, J.J.H.M. ; Said, J.M. ; Murthi, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c416t-575b9a5dc9f14ca8eff62bc720b34fc003ad08412a9fc9c2d44b665fdac1d2ad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Adult</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Fetal growth</topic><topic>Fetal Growth Retardation - metabolism</topic><topic>Glypican</topic><topic>Glypicans - metabolism</topic><topic>Heparan sulphate</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Infant, Small for Gestational Age</topic><topic>Placenta - metabolism</topic><topic>Pregnancy</topic><topic>Pregnancy Trimester, First - metabolism</topic><topic>Pregnancy Trimester, Third - metabolism</topic><topic>Proteoglycans</topic><topic>Restriction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gunatillake, T.</creatorcontrib><creatorcontrib>Chui, A.</creatorcontrib><creatorcontrib>Fitzpatrick, E.</creatorcontrib><creatorcontrib>Ignjatovic, V.</creatorcontrib><creatorcontrib>Monagle, P.</creatorcontrib><creatorcontrib>Whitelock, J.</creatorcontrib><creatorcontrib>Zanten, D.</creatorcontrib><creatorcontrib>Eijsink, J.</creatorcontrib><creatorcontrib>Borg, A.</creatorcontrib><creatorcontrib>Stevenson, J.</creatorcontrib><creatorcontrib>Brennecke, S.P.</creatorcontrib><creatorcontrib>Erwich, J.J.H.M.</creatorcontrib><creatorcontrib>Said, J.M.</creatorcontrib><creatorcontrib>Murthi, P.</creatorcontrib><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>Placenta (Eastbourne)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gunatillake, T.</au><au>Chui, A.</au><au>Fitzpatrick, E.</au><au>Ignjatovic, V.</au><au>Monagle, P.</au><au>Whitelock, J.</au><au>Zanten, D.</au><au>Eijsink, J.</au><au>Borg, A.</au><au>Stevenson, J.</au><au>Brennecke, S.P.</au><au>Erwich, J.J.H.M.</au><au>Said, J.M.</au><au>Murthi, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Decreased placental glypican expression is associated with human fetal growth restriction</atitle><jtitle>Placenta (Eastbourne)</jtitle><addtitle>Placenta</addtitle><date>2019-01-15</date><risdate>2019</risdate><volume>76</volume><spage>6</spage><epage>9</epage><pages>6-9</pages><issn>0143-4004</issn><eissn>1532-3102</eissn><abstract>Placental mediated fetal growth restriction (FGR) is a leading cause of perinatal morbidity and mortality. Heparan sulphate proteoglycans (HSPG) are highly expressed in placentae and regulate haemostasis. We hypothesise that altered expression of HSPGs, glypicans (GPC) may contribute to the development of FGR and small-for-gestational-age (SGA). GPC expression was determined in first-trimester chorionic villous samples collected from women with later SGA pregnancies and in placentae from third-trimester FGR and gestation-matched uncomplicated pregnancies. The expression of both GPC1 and GPC3 were significantly reduced in first-trimester SGA as well as in the third-trimester FGR placentae compared to controls. This is the first study to report a relationship between altered placental GPC expression and subsequent development of SGA/FGR.
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subjects | Adult Case-Control Studies Female Fetal growth Fetal Growth Retardation - metabolism Glypican Glypicans - metabolism Heparan sulphate Humans Infant, Newborn Infant, Small for Gestational Age Placenta - metabolism Pregnancy Pregnancy Trimester, First - metabolism Pregnancy Trimester, Third - metabolism Proteoglycans Restriction |
title | Decreased placental glypican expression is associated with human fetal growth restriction |
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