Expression of the insulin-like and platelet-derived growth factor genes in human uterine tissues
The human uterus repeatedly exhibits cyclic biochemical and cytological changes during the reproductive period of life. These changes are the result of a well‐characterized endocrine network involving the hypothalamus, pituitary, and ovary. The exact nature of the mechanism(s) by which the sex stero...
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Veröffentlicht in: | Molecular reproduction and development 1990-10, Vol.27 (2), p.93-101 |
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description | The human uterus repeatedly exhibits cyclic biochemical and cytological changes during the reproductive period of life. These changes are the result of a well‐characterized endocrine network involving the hypothalamus, pituitary, and ovary. The exact nature of the mechanism(s) by which the sex steroids act on the uterus remains to be elucidated. Possible local mediators of hormonal action on the uterus include polypeptide growth factors. Using the method of RNA transfer blot hybridization, we have analyzed tissue samples from the cycling human endometrium and tissue samples of human myometrium and myometrial benign tumor (leiomyoma) for the presence of platelet‐derived growth factor (PDGF) and insulin‐like growth factor (IGF) RNA. All the uterine tissues examined possessed RNA for PDGF‐B chain and IGF‐I and ‐II. Two transcripts were observed for PDGF‐B chain, four were observed for IGF‐I, and eight were observed for IGF‐II. Overall, the relative abundance of PDGF‐B chain RNA was consistent in all of the uterine tissues examined. In contrast, IGF RNA relative abundance varied. IGF‐I RNA was highest in late proliferative stage endometrium, and IGF‐II RNA was highest in early proliferative stage endometrium. Both IGF‐I and IGF‐II RNAs were greater in amount in leiomyoma than in myometrium. The increased IGF‐I RNA in late proliferative–stage human endometrium correlates with the known elevation of estradiol secretion by the ovary and the increased concentration of uterine estradiol receptors during this stage of the menstrual cycle. Furthermore, these data are consistent with reports of increased IGF‐I RNA in the rat uterus in response to administration of estradiol. Elevated levels of IGF RNA in leiomyomas may be related to the genesis and/or progression of these myometrial tumors. |
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These changes are the result of a well‐characterized endocrine network involving the hypothalamus, pituitary, and ovary. The exact nature of the mechanism(s) by which the sex steroids act on the uterus remains to be elucidated. Possible local mediators of hormonal action on the uterus include polypeptide growth factors. Using the method of RNA transfer blot hybridization, we have analyzed tissue samples from the cycling human endometrium and tissue samples of human myometrium and myometrial benign tumor (leiomyoma) for the presence of platelet‐derived growth factor (PDGF) and insulin‐like growth factor (IGF) RNA. All the uterine tissues examined possessed RNA for PDGF‐B chain and IGF‐I and ‐II. Two transcripts were observed for PDGF‐B chain, four were observed for IGF‐I, and eight were observed for IGF‐II. Overall, the relative abundance of PDGF‐B chain RNA was consistent in all of the uterine tissues examined. In contrast, IGF RNA relative abundance varied. IGF‐I RNA was highest in late proliferative stage endometrium, and IGF‐II RNA was highest in early proliferative stage endometrium. Both IGF‐I and IGF‐II RNAs were greater in amount in leiomyoma than in myometrium. The increased IGF‐I RNA in late proliferative–stage human endometrium correlates with the known elevation of estradiol secretion by the ovary and the increased concentration of uterine estradiol receptors during this stage of the menstrual cycle. Furthermore, these data are consistent with reports of increased IGF‐I RNA in the rat uterus in response to administration of estradiol. Elevated levels of IGF RNA in leiomyomas may be related to the genesis and/or progression of these myometrial tumors.</description><identifier>ISSN: 1040-452X</identifier><identifier>EISSN: 1098-2795</identifier><identifier>DOI: 10.1002/mrd.1080270203</identifier><identifier>PMID: 1979007</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Endometrium ; Endometrium - metabolism ; Female ; Gene Expression Regulation ; Humans ; Insulin-Like Growth Factor I - genetics ; Insulin-Like Growth Factor II - genetics ; Leiomyoma ; Leiomyoma - metabolism ; Menstrual cycle ; Menstrual Cycle - physiology ; Myometrium ; Myometrium - metabolism ; Platelet-Derived Growth Factor - genetics ; Poly A - biosynthesis ; Proto-Oncogene Proteins - genetics ; Proto-Oncogene Proteins c-sis ; RNA, Messenger - biosynthesis ; sis protooncogene ; Somatomedin ; Uterine Neoplasms - metabolism</subject><ispartof>Molecular reproduction and development, 1990-10, Vol.27 (2), p.93-101</ispartof><rights>Copyright © 1990 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4443-1ea87ed4224b888dd486e0dd39ee9f6959896515ee4765cf907f6abdeed7cb133</citedby><cites>FETCH-LOGICAL-c4443-1ea87ed4224b888dd486e0dd39ee9f6959896515ee4765cf907f6abdeed7cb133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fmrd.1080270203$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmrd.1080270203$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1979007$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Boehm, Keith D.</creatorcontrib><creatorcontrib>Daimon, Makoto</creatorcontrib><creatorcontrib>Gorodeski, Israel G.</creatorcontrib><creatorcontrib>Sheean, Leon A.</creatorcontrib><creatorcontrib>Utian, Wulf H.</creatorcontrib><creatorcontrib>Ilan, Judith</creatorcontrib><title>Expression of the insulin-like and platelet-derived growth factor genes in human uterine tissues</title><title>Molecular reproduction and development</title><addtitle>Mol. Reprod. Dev</addtitle><description>The human uterus repeatedly exhibits cyclic biochemical and cytological changes during the reproductive period of life. These changes are the result of a well‐characterized endocrine network involving the hypothalamus, pituitary, and ovary. The exact nature of the mechanism(s) by which the sex steroids act on the uterus remains to be elucidated. Possible local mediators of hormonal action on the uterus include polypeptide growth factors. Using the method of RNA transfer blot hybridization, we have analyzed tissue samples from the cycling human endometrium and tissue samples of human myometrium and myometrial benign tumor (leiomyoma) for the presence of platelet‐derived growth factor (PDGF) and insulin‐like growth factor (IGF) RNA. All the uterine tissues examined possessed RNA for PDGF‐B chain and IGF‐I and ‐II. Two transcripts were observed for PDGF‐B chain, four were observed for IGF‐I, and eight were observed for IGF‐II. Overall, the relative abundance of PDGF‐B chain RNA was consistent in all of the uterine tissues examined. In contrast, IGF RNA relative abundance varied. IGF‐I RNA was highest in late proliferative stage endometrium, and IGF‐II RNA was highest in early proliferative stage endometrium. Both IGF‐I and IGF‐II RNAs were greater in amount in leiomyoma than in myometrium. The increased IGF‐I RNA in late proliferative–stage human endometrium correlates with the known elevation of estradiol secretion by the ovary and the increased concentration of uterine estradiol receptors during this stage of the menstrual cycle. Furthermore, these data are consistent with reports of increased IGF‐I RNA in the rat uterus in response to administration of estradiol. Elevated levels of IGF RNA in leiomyomas may be related to the genesis and/or progression of these myometrial tumors.</description><subject>Endometrium</subject><subject>Endometrium - metabolism</subject><subject>Female</subject><subject>Gene Expression Regulation</subject><subject>Humans</subject><subject>Insulin-Like Growth Factor I - genetics</subject><subject>Insulin-Like Growth Factor II - genetics</subject><subject>Leiomyoma</subject><subject>Leiomyoma - metabolism</subject><subject>Menstrual cycle</subject><subject>Menstrual Cycle - physiology</subject><subject>Myometrium</subject><subject>Myometrium - metabolism</subject><subject>Platelet-Derived Growth Factor - genetics</subject><subject>Poly A - biosynthesis</subject><subject>Proto-Oncogene Proteins - genetics</subject><subject>Proto-Oncogene Proteins c-sis</subject><subject>RNA, Messenger - biosynthesis</subject><subject>sis protooncogene</subject><subject>Somatomedin</subject><subject>Uterine Neoplasms - metabolism</subject><issn>1040-452X</issn><issn>1098-2795</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkElLxTAUhYMozlt3Qlbuqjdt2iRL0ecADiCK4ibmNbe-aIdnkjr8eysVxZWre-B851w4hGwx2GUA6V7j7SAkpAJSyBbIKgMlk1SofPFLc0h4nt6tkLUQngBAKQnLZJkpoQDEKnmYvM89huC6lnYVjTOkrg197dqkds9ITWvpvDYRa4yJRe9e0dJH373FGa1MGTtPH7HFMKTorG9MS_s4UC3S6ELoMWyQpcrUATe_7zq5OZpcH5wkZ5fHpwf7Z0nJOc8ShkYKtDxN-VRKaS2XBYK1mUJUVaFyJVWRsxyRiyIvKwWiKszUIlpRTlmWrZOdsXfuu5fhb9SNCyXWtWmx64OWwDgAEwO4O4Kl70LwWOm5d43xH5qB_ppUD5Pq30mHwPZ3cz9t0P7i44aDr0b_zdX48U-bPr86_NOdjFkXIr7_ZI1_1oXIRK5vL471vUrFkbzKtMg-AYs6kwA</recordid><startdate>199010</startdate><enddate>199010</enddate><creator>Boehm, Keith D.</creator><creator>Daimon, Makoto</creator><creator>Gorodeski, Israel G.</creator><creator>Sheean, Leon A.</creator><creator>Utian, Wulf H.</creator><creator>Ilan, Judith</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</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>199010</creationdate><title>Expression of the insulin-like and platelet-derived growth factor genes in human uterine tissues</title><author>Boehm, Keith D. ; Daimon, Makoto ; Gorodeski, Israel G. ; Sheean, Leon A. ; Utian, Wulf H. ; Ilan, Judith</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4443-1ea87ed4224b888dd486e0dd39ee9f6959896515ee4765cf907f6abdeed7cb133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>Endometrium</topic><topic>Endometrium - metabolism</topic><topic>Female</topic><topic>Gene Expression Regulation</topic><topic>Humans</topic><topic>Insulin-Like Growth Factor I - genetics</topic><topic>Insulin-Like Growth Factor II - genetics</topic><topic>Leiomyoma</topic><topic>Leiomyoma - metabolism</topic><topic>Menstrual cycle</topic><topic>Menstrual Cycle - physiology</topic><topic>Myometrium</topic><topic>Myometrium - metabolism</topic><topic>Platelet-Derived Growth Factor - genetics</topic><topic>Poly A - biosynthesis</topic><topic>Proto-Oncogene Proteins - genetics</topic><topic>Proto-Oncogene Proteins c-sis</topic><topic>RNA, Messenger - biosynthesis</topic><topic>sis protooncogene</topic><topic>Somatomedin</topic><topic>Uterine Neoplasms - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Boehm, Keith D.</creatorcontrib><creatorcontrib>Daimon, Makoto</creatorcontrib><creatorcontrib>Gorodeski, Israel G.</creatorcontrib><creatorcontrib>Sheean, Leon A.</creatorcontrib><creatorcontrib>Utian, Wulf H.</creatorcontrib><creatorcontrib>Ilan, Judith</creatorcontrib><collection>Istex</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>Molecular reproduction and development</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Boehm, Keith D.</au><au>Daimon, Makoto</au><au>Gorodeski, Israel G.</au><au>Sheean, Leon A.</au><au>Utian, Wulf H.</au><au>Ilan, Judith</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Expression of the insulin-like and platelet-derived growth factor genes in human uterine tissues</atitle><jtitle>Molecular reproduction and development</jtitle><addtitle>Mol. Reprod. Dev</addtitle><date>1990-10</date><risdate>1990</risdate><volume>27</volume><issue>2</issue><spage>93</spage><epage>101</epage><pages>93-101</pages><issn>1040-452X</issn><eissn>1098-2795</eissn><abstract>The human uterus repeatedly exhibits cyclic biochemical and cytological changes during the reproductive period of life. These changes are the result of a well‐characterized endocrine network involving the hypothalamus, pituitary, and ovary. The exact nature of the mechanism(s) by which the sex steroids act on the uterus remains to be elucidated. Possible local mediators of hormonal action on the uterus include polypeptide growth factors. Using the method of RNA transfer blot hybridization, we have analyzed tissue samples from the cycling human endometrium and tissue samples of human myometrium and myometrial benign tumor (leiomyoma) for the presence of platelet‐derived growth factor (PDGF) and insulin‐like growth factor (IGF) RNA. All the uterine tissues examined possessed RNA for PDGF‐B chain and IGF‐I and ‐II. Two transcripts were observed for PDGF‐B chain, four were observed for IGF‐I, and eight were observed for IGF‐II. Overall, the relative abundance of PDGF‐B chain RNA was consistent in all of the uterine tissues examined. In contrast, IGF RNA relative abundance varied. IGF‐I RNA was highest in late proliferative stage endometrium, and IGF‐II RNA was highest in early proliferative stage endometrium. Both IGF‐I and IGF‐II RNAs were greater in amount in leiomyoma than in myometrium. The increased IGF‐I RNA in late proliferative–stage human endometrium correlates with the known elevation of estradiol secretion by the ovary and the increased concentration of uterine estradiol receptors during this stage of the menstrual cycle. Furthermore, these data are consistent with reports of increased IGF‐I RNA in the rat uterus in response to administration of estradiol. Elevated levels of IGF RNA in leiomyomas may be related to the genesis and/or progression of these myometrial tumors.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>1979007</pmid><doi>10.1002/mrd.1080270203</doi><tpages>9</tpages></addata></record> |
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subjects | Endometrium Endometrium - metabolism Female Gene Expression Regulation Humans Insulin-Like Growth Factor I - genetics Insulin-Like Growth Factor II - genetics Leiomyoma Leiomyoma - metabolism Menstrual cycle Menstrual Cycle - physiology Myometrium Myometrium - metabolism Platelet-Derived Growth Factor - genetics Poly A - biosynthesis Proto-Oncogene Proteins - genetics Proto-Oncogene Proteins c-sis RNA, Messenger - biosynthesis sis protooncogene Somatomedin Uterine Neoplasms - metabolism |
title | Expression of the insulin-like and platelet-derived growth factor genes in human uterine tissues |
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