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The role of insulin-like growth factor 2 mRNA binding proteins in female reproductive pathophysiology
Insulin-like growth factor 2 (IGF2) mRNA binding proteins (IMPs) family belongs to a highly conserved family of RNA-binding proteins (RBPs) and is responsible for regulating RNA processing including localization, translation and stability. Mammalian IMPs (IMP1-3) take part in development, metabolism...
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Published in: | Reproductive biology and endocrinology 2022-06, Vol.20 (1), p.89-89, Article 89 |
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description | Insulin-like growth factor 2 (IGF2) mRNA binding proteins (IMPs) family belongs to a highly conserved family of RNA-binding proteins (RBPs) and is responsible for regulating RNA processing including localization, translation and stability. Mammalian IMPs (IMP1-3) take part in development, metabolism and tumorigenesis, where they are believed to play a major role in cell growth, metabolism, migration and invasion. IMPs have been identified that are expressed in ovary, placenta and embryo. The up-to-date evidence suggest that IMPs are involved in folliculogenesis, oocyte maturation, embryogenesis, implantation, and placentation. The dysregulation of IMPs not only contributes to carcinogenesis but also disturbs the female reproduction, and may participate in the pathogenesis of reproductive diseases and obstetric syndromes, such as polycystic ovary syndrome (PCOS), pre-eclampsia (PE), gestational diabetes mellitus (GDM) and gynecological tumors. In this review, we summarize the role of IMPs in female reproductive pathophysiology, and hope to provide new insights into the identification of potential therapeutic targets. |
doi_str_mv | 10.1186/s12958-022-00960-z |
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Mammalian IMPs (IMP1-3) take part in development, metabolism and tumorigenesis, where they are believed to play a major role in cell growth, metabolism, migration and invasion. IMPs have been identified that are expressed in ovary, placenta and embryo. The up-to-date evidence suggest that IMPs are involved in folliculogenesis, oocyte maturation, embryogenesis, implantation, and placentation. The dysregulation of IMPs not only contributes to carcinogenesis but also disturbs the female reproduction, and may participate in the pathogenesis of reproductive diseases and obstetric syndromes, such as polycystic ovary syndrome (PCOS), pre-eclampsia (PE), gestational diabetes mellitus (GDM) and gynecological tumors. In this review, we summarize the role of IMPs in female reproductive pathophysiology, and hope to provide new insights into the identification of potential therapeutic targets.</description><identifier>ISSN: 1477-7827</identifier><identifier>EISSN: 1477-7827</identifier><identifier>DOI: 10.1186/s12958-022-00960-z</identifier><identifier>PMID: 35706003</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Binding proteins ; Carcinogenesis ; Cell division ; Cell growth ; Cell migration ; Diabetes ; Diabetes mellitus ; Embryogenesis ; Embryonic development ; Embryos ; Endometrium ; Female reproductive system ; Folliculogenesis ; GDM ; Genomes ; IMP ; Insulin ; Insulin-like growth factor II ; Insulin-like growth factors ; Kinases ; Localization ; Mammals ; Messenger RNA ; Metabolism ; mRNA ; Obstetrics ; Ovaries ; Ovary ; Pathogenesis ; Pathophysiology ; PCOS ; Physiological aspects ; Physiology ; Polycystic ovary syndrome ; Pre-eclampsia ; Pregnancy ; Protein binding ; Proteins ; Review ; RNA processing ; RNA-binding protein ; Stein-Leventhal syndrome ; Therapeutic targets ; Tumorigenesis</subject><ispartof>Reproductive biology and endocrinology, 2022-06, Vol.20 (1), p.89-89, Article 89</ispartof><rights>2022. The Author(s).</rights><rights>COPYRIGHT 2022 BioMed Central Ltd.</rights><rights>2022. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). 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Mammalian IMPs (IMP1-3) take part in development, metabolism and tumorigenesis, where they are believed to play a major role in cell growth, metabolism, migration and invasion. IMPs have been identified that are expressed in ovary, placenta and embryo. The up-to-date evidence suggest that IMPs are involved in folliculogenesis, oocyte maturation, embryogenesis, implantation, and placentation. The dysregulation of IMPs not only contributes to carcinogenesis but also disturbs the female reproduction, and may participate in the pathogenesis of reproductive diseases and obstetric syndromes, such as polycystic ovary syndrome (PCOS), pre-eclampsia (PE), gestational diabetes mellitus (GDM) and gynecological tumors. In this review, we summarize the role of IMPs in female reproductive pathophysiology, and hope to provide new insights into the identification of potential therapeutic targets.</description><subject>Binding proteins</subject><subject>Carcinogenesis</subject><subject>Cell division</subject><subject>Cell growth</subject><subject>Cell migration</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Embryogenesis</subject><subject>Embryonic development</subject><subject>Embryos</subject><subject>Endometrium</subject><subject>Female reproductive system</subject><subject>Folliculogenesis</subject><subject>GDM</subject><subject>Genomes</subject><subject>IMP</subject><subject>Insulin</subject><subject>Insulin-like growth factor II</subject><subject>Insulin-like growth factors</subject><subject>Kinases</subject><subject>Localization</subject><subject>Mammals</subject><subject>Messenger RNA</subject><subject>Metabolism</subject><subject>mRNA</subject><subject>Obstetrics</subject><subject>Ovaries</subject><subject>Ovary</subject><subject>Pathogenesis</subject><subject>Pathophysiology</subject><subject>PCOS</subject><subject>Physiological aspects</subject><subject>Physiology</subject><subject>Polycystic ovary syndrome</subject><subject>Pre-eclampsia</subject><subject>Pregnancy</subject><subject>Protein binding</subject><subject>Proteins</subject><subject>Review</subject><subject>RNA processing</subject><subject>RNA-binding protein</subject><subject>Stein-Leventhal syndrome</subject><subject>Therapeutic targets</subject><subject>Tumorigenesis</subject><issn>1477-7827</issn><issn>1477-7827</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptUstu1DAUjRCIlsIPsECW2LBJ8SN-bZBGFY9KFUiorC3HuU48JPHgJK2mX49nppQOQpZs6_qcc-3jUxSvCT4nRIn3E6GaqxJTWmKsBS7vnhSnpJKylIrKp4_2J8WLaVpjTDFW4nlxwrjEAmN2WsB1ByjFHlD0KIzT0oex7MNPQG2Kt3OHvHVzTIii4fvXFarD2ISxRZsUZ8jwTEEeBpv5CXKxWdwcbgBt7NzFTbedQuxju31ZPPO2n-DV_XpW_Pj08friS3n17fPlxeqqdFywuZQeOK4V51pTrglVVkCNFdOsIY5XpPYOM7CNrhxtoJFKc4ErLpyoScWoZWfF5UG3iXZtNikMNm1NtMHsCzG1xqY5uB6MpF7VrAIFeXZaKIKplzXUQmkhwWWtDwetzVIP0DgY52T7I9HjkzF0po03RhOtCcdZ4N29QIq_FphmM4TJQd_bEeIyGSqkzP-Qb56hb_-BruOSxmzVDqUIUxrLv6g2-23C6GPu63aiZiWxpLqS-7bn_0Hl0cAQXBzBh1w_ItADwaU4TQn8wxsJNrugmUPQTA6a2QfN3GXSm8fuPFD-JIv9BuIAzcU</recordid><startdate>20220615</startdate><enddate>20220615</enddate><creator>Xu, Xiao</creator><creator>Shen, Hao-Ran</creator><creator>Zhang, Jia-Rong</creator><creator>Li, Xue-Lian</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QG</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-2195-7904</orcidid></search><sort><creationdate>20220615</creationdate><title>The role of insulin-like growth factor 2 mRNA binding proteins in female reproductive pathophysiology</title><author>Xu, Xiao ; Shen, Hao-Ran ; Zhang, Jia-Rong ; Li, Xue-Lian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c563t-7fe50b85599259128a6eb08393d1c541bfc03ead94c2ded789560456c6b1432a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Binding proteins</topic><topic>Carcinogenesis</topic><topic>Cell division</topic><topic>Cell growth</topic><topic>Cell migration</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Embryogenesis</topic><topic>Embryonic development</topic><topic>Embryos</topic><topic>Endometrium</topic><topic>Female reproductive system</topic><topic>Folliculogenesis</topic><topic>GDM</topic><topic>Genomes</topic><topic>IMP</topic><topic>Insulin</topic><topic>Insulin-like growth factor II</topic><topic>Insulin-like growth factors</topic><topic>Kinases</topic><topic>Localization</topic><topic>Mammals</topic><topic>Messenger RNA</topic><topic>Metabolism</topic><topic>mRNA</topic><topic>Obstetrics</topic><topic>Ovaries</topic><topic>Ovary</topic><topic>Pathogenesis</topic><topic>Pathophysiology</topic><topic>PCOS</topic><topic>Physiological aspects</topic><topic>Physiology</topic><topic>Polycystic ovary syndrome</topic><topic>Pre-eclampsia</topic><topic>Pregnancy</topic><topic>Protein binding</topic><topic>Proteins</topic><topic>Review</topic><topic>RNA processing</topic><topic>RNA-binding protein</topic><topic>Stein-Leventhal syndrome</topic><topic>Therapeutic targets</topic><topic>Tumorigenesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xu, Xiao</creatorcontrib><creatorcontrib>Shen, Hao-Ran</creatorcontrib><creatorcontrib>Zhang, Jia-Rong</creatorcontrib><creatorcontrib>Li, Xue-Lian</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Animal Behavior Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>British Nursing Database</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Reproductive biology and endocrinology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xu, Xiao</au><au>Shen, Hao-Ran</au><au>Zhang, Jia-Rong</au><au>Li, Xue-Lian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of insulin-like growth factor 2 mRNA binding proteins in female reproductive pathophysiology</atitle><jtitle>Reproductive biology and endocrinology</jtitle><addtitle>Reprod Biol Endocrinol</addtitle><date>2022-06-15</date><risdate>2022</risdate><volume>20</volume><issue>1</issue><spage>89</spage><epage>89</epage><pages>89-89</pages><artnum>89</artnum><issn>1477-7827</issn><eissn>1477-7827</eissn><abstract>Insulin-like growth factor 2 (IGF2) mRNA binding proteins (IMPs) family belongs to a highly conserved family of RNA-binding proteins (RBPs) and is responsible for regulating RNA processing including localization, translation and stability. Mammalian IMPs (IMP1-3) take part in development, metabolism and tumorigenesis, where they are believed to play a major role in cell growth, metabolism, migration and invasion. IMPs have been identified that are expressed in ovary, placenta and embryo. The up-to-date evidence suggest that IMPs are involved in folliculogenesis, oocyte maturation, embryogenesis, implantation, and placentation. The dysregulation of IMPs not only contributes to carcinogenesis but also disturbs the female reproduction, and may participate in the pathogenesis of reproductive diseases and obstetric syndromes, such as polycystic ovary syndrome (PCOS), pre-eclampsia (PE), gestational diabetes mellitus (GDM) and gynecological tumors. In this review, we summarize the role of IMPs in female reproductive pathophysiology, and hope to provide new insights into the identification of potential therapeutic targets.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>35706003</pmid><doi>10.1186/s12958-022-00960-z</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0003-2195-7904</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Binding proteins Carcinogenesis Cell division Cell growth Cell migration Diabetes Diabetes mellitus Embryogenesis Embryonic development Embryos Endometrium Female reproductive system Folliculogenesis GDM Genomes IMP Insulin Insulin-like growth factor II Insulin-like growth factors Kinases Localization Mammals Messenger RNA Metabolism mRNA Obstetrics Ovaries Ovary Pathogenesis Pathophysiology PCOS Physiological aspects Physiology Polycystic ovary syndrome Pre-eclampsia Pregnancy Protein binding Proteins Review RNA processing RNA-binding protein Stein-Leventhal syndrome Therapeutic targets Tumorigenesis |
title | The role of insulin-like growth factor 2 mRNA binding proteins in female reproductive pathophysiology |
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