Regulation of Prolactin Receptor Levels and Activity in Breast Cancer

From its traditional identity as a hormone involved in growth and differentiation of mammary epithelium and in lactation, to having a pertinent role in the development of mammary carcinoma, the peptide hormone/cytokine prolactin (PRL) has emerged as a versatile signaling molecule. There has been sig...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of mammary gland biology and neoplasia 2008-03, Vol.13 (1), p.81-91
Hauptverfasser: Swaminathan, G, Varghese, B, Fuchs, S. Y
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 91
container_issue 1
container_start_page 81
container_title Journal of mammary gland biology and neoplasia
container_volume 13
creator Swaminathan, G
Varghese, B
Fuchs, S. Y
description From its traditional identity as a hormone involved in growth and differentiation of mammary epithelium and in lactation, to having a pertinent role in the development of mammary carcinoma, the peptide hormone/cytokine prolactin (PRL) has emerged as a versatile signaling molecule. There has been significant progress in our understanding of the fine working of PRL in the past several years. Notably, much effort has been concentrated on the mediator of PRL action, namely, the prolactin receptor (PRLr). The causal link between increased PRLr expression and breast cancer is being increasingly appreciated. Considering that the level of the receptor on the surface is a critical determinant of signaling output in response to PRL, the uncovering of regulatory elements that control receptor expression becomes important. The principle focus of this review is on the regulation of PRLr expression and activity in breast cancer with a brief overview of different isoforms of PRLr, their expression, signaling capabilities and the biological outcomes of PRL/PRLr signaling.
doi_str_mv 10.1007/s10911-008-9068-6
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2276629</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>70341198</sourcerecordid><originalsourceid>FETCH-LOGICAL-c491t-2ea48fb4531705932b025e44342b97ee43d822de56ce6b69969ab2326be33b33</originalsourceid><addsrcrecordid>eNp9kU9v1DAQxS1ERf_AB-DSRhx6C4zHjmNfkMqqBaSVQKWcLSc7WVJl7a2drNRvX1dZUcqhJ1t6v_c848fYew4fOUD9KXEwnJcAujSgdKlesSNe1aKsQZjX-Q5alAKQH7LjlG4BwGhVvWGHXCNIo_GIXV7Tehrc2AdfhK74GcPg2rH3xTW1tB1DLJa0oyEVzq-Ki6zs-vG-yPqXSC6NxcL5luJbdtC5IdG7_XnCbq4ubxbfyuWPr98XF8uylYaPJZKTumtkJXgNlRHYAFYkpZDYmJpIipVGXFGlWlKNMkYZ16BA1ZAQjRAn7PMcu52aDa1a8mN0g93GfuPivQ2ut88V3_-x67CziLVSaHLA-T4ghruJ0mg3fWppGJynMCWb_01ybnQGP_wH3oYp-rybRW5QaF7XGeIz1MaQUqTu7yQc7GNBdi7I5oLsY0FWZc_pvys8OfaNZABnIGXJryk-vfxS6tls6lywbh37ZH__QuAiM0pqheIBCMKj2w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>219238177</pqid></control><display><type>article</type><title>Regulation of Prolactin Receptor Levels and Activity in Breast Cancer</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Swaminathan, G ; Varghese, B ; Fuchs, S. Y</creator><creatorcontrib>Swaminathan, G ; Varghese, B ; Fuchs, S. Y</creatorcontrib><description>From its traditional identity as a hormone involved in growth and differentiation of mammary epithelium and in lactation, to having a pertinent role in the development of mammary carcinoma, the peptide hormone/cytokine prolactin (PRL) has emerged as a versatile signaling molecule. There has been significant progress in our understanding of the fine working of PRL in the past several years. Notably, much effort has been concentrated on the mediator of PRL action, namely, the prolactin receptor (PRLr). The causal link between increased PRLr expression and breast cancer is being increasingly appreciated. Considering that the level of the receptor on the surface is a critical determinant of signaling output in response to PRL, the uncovering of regulatory elements that control receptor expression becomes important. The principle focus of this review is on the regulation of PRLr expression and activity in breast cancer with a brief overview of different isoforms of PRLr, their expression, signaling capabilities and the biological outcomes of PRL/PRLr signaling.</description><identifier>ISSN: 1083-3021</identifier><identifier>EISSN: 1573-7039</identifier><identifier>DOI: 10.1007/s10911-008-9068-6</identifier><identifier>PMID: 18204982</identifier><language>eng</language><publisher>Boston: Boston : Springer US</publisher><subject>Animals ; Breast cancer ; breast neoplasms ; Breast Neoplasms - genetics ; Breast Neoplasms - metabolism ; Cancer Research ; endocytosis ; Gene Expression Regulation, Neoplastic ; Humans ; Medicine ; Medicine &amp; Public Health ; Oncology ; Prolactin receptor ; Protein Isoforms - chemistry ; Protein Isoforms - metabolism ; Receptors, Prolactin - chemistry ; Receptors, Prolactin - genetics ; Receptors, Prolactin - metabolism ; Regulation ; Signal Transduction ; Signaling ; Ubiquitin - metabolism ; Ubiquitination</subject><ispartof>Journal of mammary gland biology and neoplasia, 2008-03, Vol.13 (1), p.81-91</ispartof><rights>Springer Science+Business Media, LLC 2008</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c491t-2ea48fb4531705932b025e44342b97ee43d822de56ce6b69969ab2326be33b33</citedby><cites>FETCH-LOGICAL-c491t-2ea48fb4531705932b025e44342b97ee43d822de56ce6b69969ab2326be33b33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10911-008-9068-6$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10911-008-9068-6$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,777,781,882,27905,27906,41469,42538,51300</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18204982$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Swaminathan, G</creatorcontrib><creatorcontrib>Varghese, B</creatorcontrib><creatorcontrib>Fuchs, S. Y</creatorcontrib><title>Regulation of Prolactin Receptor Levels and Activity in Breast Cancer</title><title>Journal of mammary gland biology and neoplasia</title><addtitle>J Mammary Gland Biol Neoplasia</addtitle><addtitle>J Mammary Gland Biol Neoplasia</addtitle><description>From its traditional identity as a hormone involved in growth and differentiation of mammary epithelium and in lactation, to having a pertinent role in the development of mammary carcinoma, the peptide hormone/cytokine prolactin (PRL) has emerged as a versatile signaling molecule. There has been significant progress in our understanding of the fine working of PRL in the past several years. Notably, much effort has been concentrated on the mediator of PRL action, namely, the prolactin receptor (PRLr). The causal link between increased PRLr expression and breast cancer is being increasingly appreciated. Considering that the level of the receptor on the surface is a critical determinant of signaling output in response to PRL, the uncovering of regulatory elements that control receptor expression becomes important. The principle focus of this review is on the regulation of PRLr expression and activity in breast cancer with a brief overview of different isoforms of PRLr, their expression, signaling capabilities and the biological outcomes of PRL/PRLr signaling.</description><subject>Animals</subject><subject>Breast cancer</subject><subject>breast neoplasms</subject><subject>Breast Neoplasms - genetics</subject><subject>Breast Neoplasms - metabolism</subject><subject>Cancer Research</subject><subject>endocytosis</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Oncology</subject><subject>Prolactin receptor</subject><subject>Protein Isoforms - chemistry</subject><subject>Protein Isoforms - metabolism</subject><subject>Receptors, Prolactin - chemistry</subject><subject>Receptors, Prolactin - genetics</subject><subject>Receptors, Prolactin - metabolism</subject><subject>Regulation</subject><subject>Signal Transduction</subject><subject>Signaling</subject><subject>Ubiquitin - metabolism</subject><subject>Ubiquitination</subject><issn>1083-3021</issn><issn>1573-7039</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNp9kU9v1DAQxS1ERf_AB-DSRhx6C4zHjmNfkMqqBaSVQKWcLSc7WVJl7a2drNRvX1dZUcqhJ1t6v_c848fYew4fOUD9KXEwnJcAujSgdKlesSNe1aKsQZjX-Q5alAKQH7LjlG4BwGhVvWGHXCNIo_GIXV7Tehrc2AdfhK74GcPg2rH3xTW1tB1DLJa0oyEVzq-Ki6zs-vG-yPqXSC6NxcL5luJbdtC5IdG7_XnCbq4ubxbfyuWPr98XF8uylYaPJZKTumtkJXgNlRHYAFYkpZDYmJpIipVGXFGlWlKNMkYZ16BA1ZAQjRAn7PMcu52aDa1a8mN0g93GfuPivQ2ut88V3_-x67CziLVSaHLA-T4ghruJ0mg3fWppGJynMCWb_01ybnQGP_wH3oYp-rybRW5QaF7XGeIz1MaQUqTu7yQc7GNBdi7I5oLsY0FWZc_pvys8OfaNZABnIGXJryk-vfxS6tls6lywbh37ZH__QuAiM0pqheIBCMKj2w</recordid><startdate>20080301</startdate><enddate>20080301</enddate><creator>Swaminathan, G</creator><creator>Varghese, B</creator><creator>Fuchs, S. Y</creator><general>Boston : Springer US</general><general>Springer US</general><general>Springer Nature B.V</general><scope>FBQ</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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20080301</creationdate><title>Regulation of Prolactin Receptor Levels and Activity in Breast Cancer</title><author>Swaminathan, G ; Varghese, B ; Fuchs, S. Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c491t-2ea48fb4531705932b025e44342b97ee43d822de56ce6b69969ab2326be33b33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Animals</topic><topic>Breast cancer</topic><topic>breast neoplasms</topic><topic>Breast Neoplasms - genetics</topic><topic>Breast Neoplasms - metabolism</topic><topic>Cancer Research</topic><topic>endocytosis</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Oncology</topic><topic>Prolactin receptor</topic><topic>Protein Isoforms - chemistry</topic><topic>Protein Isoforms - metabolism</topic><topic>Receptors, Prolactin - chemistry</topic><topic>Receptors, Prolactin - genetics</topic><topic>Receptors, Prolactin - metabolism</topic><topic>Regulation</topic><topic>Signal Transduction</topic><topic>Signaling</topic><topic>Ubiquitin - metabolism</topic><topic>Ubiquitination</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Swaminathan, G</creatorcontrib><creatorcontrib>Varghese, B</creatorcontrib><creatorcontrib>Fuchs, S. Y</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</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 Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science 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><jtitle>Journal of mammary gland biology and neoplasia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Swaminathan, G</au><au>Varghese, B</au><au>Fuchs, S. Y</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of Prolactin Receptor Levels and Activity in Breast Cancer</atitle><jtitle>Journal of mammary gland biology and neoplasia</jtitle><stitle>J Mammary Gland Biol Neoplasia</stitle><addtitle>J Mammary Gland Biol Neoplasia</addtitle><date>2008-03-01</date><risdate>2008</risdate><volume>13</volume><issue>1</issue><spage>81</spage><epage>91</epage><pages>81-91</pages><issn>1083-3021</issn><eissn>1573-7039</eissn><abstract>From its traditional identity as a hormone involved in growth and differentiation of mammary epithelium and in lactation, to having a pertinent role in the development of mammary carcinoma, the peptide hormone/cytokine prolactin (PRL) has emerged as a versatile signaling molecule. There has been significant progress in our understanding of the fine working of PRL in the past several years. Notably, much effort has been concentrated on the mediator of PRL action, namely, the prolactin receptor (PRLr). The causal link between increased PRLr expression and breast cancer is being increasingly appreciated. Considering that the level of the receptor on the surface is a critical determinant of signaling output in response to PRL, the uncovering of regulatory elements that control receptor expression becomes important. The principle focus of this review is on the regulation of PRLr expression and activity in breast cancer with a brief overview of different isoforms of PRLr, their expression, signaling capabilities and the biological outcomes of PRL/PRLr signaling.</abstract><cop>Boston</cop><pub>Boston : Springer US</pub><pmid>18204982</pmid><doi>10.1007/s10911-008-9068-6</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1083-3021
ispartof Journal of mammary gland biology and neoplasia, 2008-03, Vol.13 (1), p.81-91
issn 1083-3021
1573-7039
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_2276629
source MEDLINE; Springer Nature - Complete Springer Journals
subjects Animals
Breast cancer
breast neoplasms
Breast Neoplasms - genetics
Breast Neoplasms - metabolism
Cancer Research
endocytosis
Gene Expression Regulation, Neoplastic
Humans
Medicine
Medicine & Public Health
Oncology
Prolactin receptor
Protein Isoforms - chemistry
Protein Isoforms - metabolism
Receptors, Prolactin - chemistry
Receptors, Prolactin - genetics
Receptors, Prolactin - metabolism
Regulation
Signal Transduction
Signaling
Ubiquitin - metabolism
Ubiquitination
title Regulation of Prolactin Receptor Levels and Activity in Breast Cancer
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-20T17%3A56%3A48IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Regulation%20of%20Prolactin%20Receptor%20Levels%20and%20Activity%20in%20Breast%20Cancer&rft.jtitle=Journal%20of%20mammary%20gland%20biology%20and%20neoplasia&rft.au=Swaminathan,%20G&rft.date=2008-03-01&rft.volume=13&rft.issue=1&rft.spage=81&rft.epage=91&rft.pages=81-91&rft.issn=1083-3021&rft.eissn=1573-7039&rft_id=info:doi/10.1007/s10911-008-9068-6&rft_dat=%3Cproquest_pubme%3E70341198%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=219238177&rft_id=info:pmid/18204982&rfr_iscdi=true