Role of prolactin in growth of the rat mammary tumor MTW9
The growth of MTW9 mammary tumors exhibits different degrees of responsiveness to ovariectomy, ranging from sensitivity to resistance. This range of response is a function of time elapsing from tumor inoculation until performance of ovariectomy provided that prolactin (PRL) level is kept continuousl...
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Veröffentlicht in: | International journal of cancer 1991-04, Vol.48 (1), p.109-112 |
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description | The growth of MTW9 mammary tumors exhibits different degrees of responsiveness to ovariectomy, ranging from sensitivity to resistance. This range of response is a function of time elapsing from tumor inoculation until performance of ovariectomy provided that prolactin (PRL) level is kept continuously high. In vivo studies showed that the MTW9 tumors developed by chronic administration of spiramide were sensitive to ovariectomy by 60 days, but they became resistant to ovariectomy by 100 days. However, when spiramide treatment was discontinued after tumor appearance, the tumors were still sensitive to ovariectomy by 100 days. Chromatofo‐cusing (CF) profile of cytosolic estrogen receptors (ER) correlated with the responsiveness to ovariectomy. A 2‐peak profile for tumors sensitive to ovariectomy, and only a one‐peak profile for tumors resistant to ovariectomy, were seen. Although the prolactin level in rats bearing the tumors was higher than in the normal rats, no correlation between the PRL level and the change in CF profile of ER over time was seen. Also, these changes could not be correlated with the tumor size. In vitro studies showed that incubation of cytosolic ER from a sensitive tumor (2 peaks) with PRL led to a CF profile with only one peak, characteristic of a resistant tumor. Leupeptin, molybdate and phenylmethylsulfonylfluoride (PMSF) could not prevent this transition. The effect was not reproduced by incubation with growth hormone or progesterone. Our data suggest that PRL, either directly or through intermediates, may play a role in changing the response to hormonal therapy of the mammary tumor MTW9. |
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This range of response is a function of time elapsing from tumor inoculation until performance of ovariectomy provided that prolactin (PRL) level is kept continuously high. In vivo studies showed that the MTW9 tumors developed by chronic administration of spiramide were sensitive to ovariectomy by 60 days, but they became resistant to ovariectomy by 100 days. However, when spiramide treatment was discontinued after tumor appearance, the tumors were still sensitive to ovariectomy by 100 days. Chromatofo‐cusing (CF) profile of cytosolic estrogen receptors (ER) correlated with the responsiveness to ovariectomy. A 2‐peak profile for tumors sensitive to ovariectomy, and only a one‐peak profile for tumors resistant to ovariectomy, were seen. Although the prolactin level in rats bearing the tumors was higher than in the normal rats, no correlation between the PRL level and the change in CF profile of ER over time was seen. Also, these changes could not be correlated with the tumor size. In vitro studies showed that incubation of cytosolic ER from a sensitive tumor (2 peaks) with PRL led to a CF profile with only one peak, characteristic of a resistant tumor. Leupeptin, molybdate and phenylmethylsulfonylfluoride (PMSF) could not prevent this transition. The effect was not reproduced by incubation with growth hormone or progesterone. Our data suggest that PRL, either directly or through intermediates, may play a role in changing the response to hormonal therapy of the mammary tumor MTW9.</description><identifier>ISSN: 0020-7136</identifier><identifier>EISSN: 1097-0215</identifier><identifier>DOI: 10.1002/ijc.2910480120</identifier><identifier>PMID: 2019452</identifier><identifier>CODEN: IJCNAW</identifier><language>eng</language><publisher>New York: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Animal tumors. Experimental tumors ; Animals ; Biological and medical sciences ; Cell Division - drug effects ; Cytosol - chemistry ; Experimental genital and mammary tumors ; Female ; Mammary Neoplasms, Experimental - pathology ; Medical sciences ; Ovariectomy ; Pituitary Neoplasms - pathology ; Prolactin - pharmacology ; Prolactin - physiology ; Rats ; Receptors, Estrogen - analysis ; Receptors, Estrogen - biosynthesis ; Receptors, Estrogen - drug effects ; Spiro Compounds - pharmacology ; Tranquilizing Agents - pharmacology ; Tumors</subject><ispartof>International journal of cancer, 1991-04, Vol.48 (1), p.109-112</ispartof><rights>Copyright © 1991 Wiley‐Liss, Inc., A Wiley Company</rights><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3700-74b64bc120b508674f11c38cf5eb82663ec11f26b748e85397541e0e4232705b3</citedby><cites>FETCH-LOGICAL-c3700-74b64bc120b508674f11c38cf5eb82663ec11f26b748e85397541e0e4232705b3</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%2Fijc.2910480120$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fijc.2910480120$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19819109$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2019452$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Platica, Micsunica</creatorcontrib><creatorcontrib>Doody, Jacqueline</creatorcontrib><creatorcontrib>Mandeli, John P.</creatorcontrib><creatorcontrib>Hollander, Vincent P.</creatorcontrib><title>Role of prolactin in growth of the rat mammary tumor MTW9</title><title>International journal of cancer</title><addtitle>Int J Cancer</addtitle><description>The growth of MTW9 mammary tumors exhibits different degrees of responsiveness to ovariectomy, ranging from sensitivity to resistance. This range of response is a function of time elapsing from tumor inoculation until performance of ovariectomy provided that prolactin (PRL) level is kept continuously high. In vivo studies showed that the MTW9 tumors developed by chronic administration of spiramide were sensitive to ovariectomy by 60 days, but they became resistant to ovariectomy by 100 days. However, when spiramide treatment was discontinued after tumor appearance, the tumors were still sensitive to ovariectomy by 100 days. Chromatofo‐cusing (CF) profile of cytosolic estrogen receptors (ER) correlated with the responsiveness to ovariectomy. A 2‐peak profile for tumors sensitive to ovariectomy, and only a one‐peak profile for tumors resistant to ovariectomy, were seen. Although the prolactin level in rats bearing the tumors was higher than in the normal rats, no correlation between the PRL level and the change in CF profile of ER over time was seen. Also, these changes could not be correlated with the tumor size. In vitro studies showed that incubation of cytosolic ER from a sensitive tumor (2 peaks) with PRL led to a CF profile with only one peak, characteristic of a resistant tumor. Leupeptin, molybdate and phenylmethylsulfonylfluoride (PMSF) could not prevent this transition. The effect was not reproduced by incubation with growth hormone or progesterone. Our data suggest that PRL, either directly or through intermediates, may play a role in changing the response to hormonal therapy of the mammary tumor MTW9.</description><subject>Animal tumors. Experimental tumors</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Cell Division - drug effects</subject><subject>Cytosol - chemistry</subject><subject>Experimental genital and mammary tumors</subject><subject>Female</subject><subject>Mammary Neoplasms, Experimental - pathology</subject><subject>Medical sciences</subject><subject>Ovariectomy</subject><subject>Pituitary Neoplasms - pathology</subject><subject>Prolactin - pharmacology</subject><subject>Prolactin - physiology</subject><subject>Rats</subject><subject>Receptors, Estrogen - analysis</subject><subject>Receptors, Estrogen - biosynthesis</subject><subject>Receptors, Estrogen - drug effects</subject><subject>Spiro Compounds - pharmacology</subject><subject>Tranquilizing Agents - pharmacology</subject><subject>Tumors</subject><issn>0020-7136</issn><issn>1097-0215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1Lw0AQxRdRaq1evQm56C11ZrOb3T1K8aNSEaTiMWzWjU1JmrqbUPrfu6XBehMGBmZ-8-bxCLlEGCMAvS2XZkwVApOAFI7IEEGJGCjyYzIMAMQCk_SUnHm_BEDkwAZkQAEV43RI1FtT2agporVrKm3achWF-nLNpl3sxu3CRk63Ua3rWrtt1HZ146KX-Yc6JyeFrry96PuIvD_czydP8ez1cTq5m8UmERC-szxluQnecg4yFaxANIk0Bbe5pGmaWINY0DQXTFrJEyU4QwuW0YQK4HkyIjd73eDwu7O-zerSG1tVemWbzmcSOBWCQQDHe9C4xntni2ztyp3pDCHbZZWFrLJDVuHgqlfu8tp-_uJ9OGF_3e-1N7oqnF6Z0h9UlcQgpgKn9tymrOz2n6_Z9Hnyx8MPR7h-zQ</recordid><startdate>19910422</startdate><enddate>19910422</enddate><creator>Platica, Micsunica</creator><creator>Doody, Jacqueline</creator><creator>Mandeli, John P.</creator><creator>Hollander, Vincent P.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</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>19910422</creationdate><title>Role of prolactin in growth of the rat mammary tumor MTW9</title><author>Platica, Micsunica ; Doody, Jacqueline ; Mandeli, John P. ; Hollander, Vincent P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3700-74b64bc120b508674f11c38cf5eb82663ec11f26b748e85397541e0e4232705b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Animal tumors. Experimental tumors</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Cell Division - drug effects</topic><topic>Cytosol - chemistry</topic><topic>Experimental genital and mammary tumors</topic><topic>Female</topic><topic>Mammary Neoplasms, Experimental - pathology</topic><topic>Medical sciences</topic><topic>Ovariectomy</topic><topic>Pituitary Neoplasms - pathology</topic><topic>Prolactin - pharmacology</topic><topic>Prolactin - physiology</topic><topic>Rats</topic><topic>Receptors, Estrogen - analysis</topic><topic>Receptors, Estrogen - biosynthesis</topic><topic>Receptors, Estrogen - drug effects</topic><topic>Spiro Compounds - pharmacology</topic><topic>Tranquilizing Agents - pharmacology</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Platica, Micsunica</creatorcontrib><creatorcontrib>Doody, Jacqueline</creatorcontrib><creatorcontrib>Mandeli, John P.</creatorcontrib><creatorcontrib>Hollander, Vincent P.</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>International journal of cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Platica, Micsunica</au><au>Doody, Jacqueline</au><au>Mandeli, John P.</au><au>Hollander, Vincent P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of prolactin in growth of the rat mammary tumor MTW9</atitle><jtitle>International journal of cancer</jtitle><addtitle>Int J Cancer</addtitle><date>1991-04-22</date><risdate>1991</risdate><volume>48</volume><issue>1</issue><spage>109</spage><epage>112</epage><pages>109-112</pages><issn>0020-7136</issn><eissn>1097-0215</eissn><coden>IJCNAW</coden><abstract>The growth of MTW9 mammary tumors exhibits different degrees of responsiveness to ovariectomy, ranging from sensitivity to resistance. This range of response is a function of time elapsing from tumor inoculation until performance of ovariectomy provided that prolactin (PRL) level is kept continuously high. In vivo studies showed that the MTW9 tumors developed by chronic administration of spiramide were sensitive to ovariectomy by 60 days, but they became resistant to ovariectomy by 100 days. However, when spiramide treatment was discontinued after tumor appearance, the tumors were still sensitive to ovariectomy by 100 days. Chromatofo‐cusing (CF) profile of cytosolic estrogen receptors (ER) correlated with the responsiveness to ovariectomy. A 2‐peak profile for tumors sensitive to ovariectomy, and only a one‐peak profile for tumors resistant to ovariectomy, were seen. Although the prolactin level in rats bearing the tumors was higher than in the normal rats, no correlation between the PRL level and the change in CF profile of ER over time was seen. Also, these changes could not be correlated with the tumor size. In vitro studies showed that incubation of cytosolic ER from a sensitive tumor (2 peaks) with PRL led to a CF profile with only one peak, characteristic of a resistant tumor. Leupeptin, molybdate and phenylmethylsulfonylfluoride (PMSF) could not prevent this transition. The effect was not reproduced by incubation with growth hormone or progesterone. Our data suggest that PRL, either directly or through intermediates, may play a role in changing the response to hormonal therapy of the mammary tumor MTW9.</abstract><cop>New York</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>2019452</pmid><doi>10.1002/ijc.2910480120</doi><tpages>4</tpages></addata></record> |
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subjects | Animal tumors. Experimental tumors Animals Biological and medical sciences Cell Division - drug effects Cytosol - chemistry Experimental genital and mammary tumors Female Mammary Neoplasms, Experimental - pathology Medical sciences Ovariectomy Pituitary Neoplasms - pathology Prolactin - pharmacology Prolactin - physiology Rats Receptors, Estrogen - analysis Receptors, Estrogen - biosynthesis Receptors, Estrogen - drug effects Spiro Compounds - pharmacology Tranquilizing Agents - pharmacology Tumors |
title | Role of prolactin in growth of the rat mammary tumor MTW9 |
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