Control of peripheral benzodiazepine receptor-mediated breast cancer in rats by soy protein

Soy protein is known to have breast tumor suppressing activity. The expression of peripheral benzodiazepine receptors (PBRs), currently renamed as translocator protein (TSPO) and their associated functions, such as nuclear cholesterol uptake and content also have been shown to be increased in breast...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Molecular carcinogenesis 2008-04, Vol.47 (4), p.310-319
Hauptverfasser: Mukhopadhyay, Sutapa, Rajaratnam, Veera, Mukherjee, Shyamali, Das, Salil K.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 319
container_issue 4
container_start_page 310
container_title Molecular carcinogenesis
container_volume 47
creator Mukhopadhyay, Sutapa
Rajaratnam, Veera
Mukherjee, Shyamali
Das, Salil K.
description Soy protein is known to have breast tumor suppressing activity. The expression of peripheral benzodiazepine receptors (PBRs), currently renamed as translocator protein (TSPO) and their associated functions, such as nuclear cholesterol uptake and content also have been shown to be increased in breast cancer. Here we investigated whether the breast tumor suppressing effects of soy protein is mediated by down‐regulation of PBR expression and function. Breast tumors were induced by gavage administration of a single dose (80 mg/kg) of dimethylbenz[a]anthracene (DMBA) into 50‐d old female Sprague Dawley rats, maintained on a standard AIN‐76A diet containing either casein or soy protein. Approximately 120 d following DMBA administration, the animals were sacrificed. All tumors were detected by palpation and at autopsy biopsy specimens were taken for histological grading. The ligand binding capacity, expression, and protein levels of PBRs, their nuclear localization and function, such as nuclear cholesterol uptake and content, were significantly increased in the tumors. However, replacement of casein by soy protein in the diet caused a significant decrease in all of these parameters. These data suggest that soy protein inhibits breast tumor development by decreasing the expression of the tumor‐promoting gene, which encodes PBRs. © 2007 Wiley‐Liss, Inc.
doi_str_mv 10.1002/mc.20387
format Article
fullrecord <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_mc_20387</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_ZBZD2105_0</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3577-4dae6949fa6067b18891dd3090c91524a13da0535c84b8d0d0dd03fad6d7264a3</originalsourceid><addsrcrecordid>eNp10E1LxDAQBuAgiruugr9AcvTSddK0TXPUqquw6kUR1kNIkylWtx8kFe3-equ76knmMDA8vDAvIYcMpgwgPKnMNASeii0yZiDTIBRRtE3GkEoZMJmKEdnz_gWAMRHDLhkxIXkoIzEmT1lTd65Z0qagLbqyfUanlzTHetXYUq-wLWukDg22XeOCCodjh5bmDrXvqNG1QUfLmjrdeZr31Dc9bV3TYVnvk51CLz0ebPaEPFxe3GdXwfxudp2dzgPDYyGCyGpMZCQLnUAicpamklnLQYKRLA4jzbjVEPPYpFGeWhjGAi-0TawIk0jzCTle5xrXeO-wUK0rK-16xUB99aMqo777GejRmrZv-fDLH9wUMoBgDd7LJfb_Bqmb7Cdw40vf4cev1-5VJYKLWD3eztTibHEeMogV8E8iIH3x</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Control of peripheral benzodiazepine receptor-mediated breast cancer in rats by soy protein</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>Mukhopadhyay, Sutapa ; Rajaratnam, Veera ; Mukherjee, Shyamali ; Das, Salil K.</creator><creatorcontrib>Mukhopadhyay, Sutapa ; Rajaratnam, Veera ; Mukherjee, Shyamali ; Das, Salil K.</creatorcontrib><description>Soy protein is known to have breast tumor suppressing activity. The expression of peripheral benzodiazepine receptors (PBRs), currently renamed as translocator protein (TSPO) and their associated functions, such as nuclear cholesterol uptake and content also have been shown to be increased in breast cancer. Here we investigated whether the breast tumor suppressing effects of soy protein is mediated by down‐regulation of PBR expression and function. Breast tumors were induced by gavage administration of a single dose (80 mg/kg) of dimethylbenz[a]anthracene (DMBA) into 50‐d old female Sprague Dawley rats, maintained on a standard AIN‐76A diet containing either casein or soy protein. Approximately 120 d following DMBA administration, the animals were sacrificed. All tumors were detected by palpation and at autopsy biopsy specimens were taken for histological grading. The ligand binding capacity, expression, and protein levels of PBRs, their nuclear localization and function, such as nuclear cholesterol uptake and content, were significantly increased in the tumors. However, replacement of casein by soy protein in the diet caused a significant decrease in all of these parameters. These data suggest that soy protein inhibits breast tumor development by decreasing the expression of the tumor‐promoting gene, which encodes PBRs. © 2007 Wiley‐Liss, Inc.</description><identifier>ISSN: 0899-1987</identifier><identifier>EISSN: 1098-2744</identifier><identifier>DOI: 10.1002/mc.20387</identifier><identifier>PMID: 17932947</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>9,10-Dimethyl-1,2-benzanthracene - pharmacology ; Animals ; Benzodiazepinones - metabolism ; breast cancer ; Carcinogens - pharmacology ; Female ; Ligands ; Mammary Neoplasms, Experimental - chemically induced ; Mammary Neoplasms, Experimental - diet therapy ; Mammary Neoplasms, Experimental - metabolism ; PBRs ; Protein Binding ; Rats ; Rats, Sprague-Dawley ; Receptors, GABA-A - metabolism ; Receptors, GABA-A - physiology ; soy protein ; Soybean Proteins - administration &amp; dosage ; Soybean Proteins - therapeutic use ; Tritium - metabolism</subject><ispartof>Molecular carcinogenesis, 2008-04, Vol.47 (4), p.310-319</ispartof><rights>Copyright © 2007 Wiley‐Liss, Inc.</rights><rights>(c) 2007 Wiley-Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3577-4dae6949fa6067b18891dd3090c91524a13da0535c84b8d0d0dd03fad6d7264a3</citedby><cites>FETCH-LOGICAL-c3577-4dae6949fa6067b18891dd3090c91524a13da0535c84b8d0d0dd03fad6d7264a3</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%2Fmc.20387$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmc.20387$$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/17932947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mukhopadhyay, Sutapa</creatorcontrib><creatorcontrib>Rajaratnam, Veera</creatorcontrib><creatorcontrib>Mukherjee, Shyamali</creatorcontrib><creatorcontrib>Das, Salil K.</creatorcontrib><title>Control of peripheral benzodiazepine receptor-mediated breast cancer in rats by soy protein</title><title>Molecular carcinogenesis</title><addtitle>Mol. Carcinog</addtitle><description>Soy protein is known to have breast tumor suppressing activity. The expression of peripheral benzodiazepine receptors (PBRs), currently renamed as translocator protein (TSPO) and their associated functions, such as nuclear cholesterol uptake and content also have been shown to be increased in breast cancer. Here we investigated whether the breast tumor suppressing effects of soy protein is mediated by down‐regulation of PBR expression and function. Breast tumors were induced by gavage administration of a single dose (80 mg/kg) of dimethylbenz[a]anthracene (DMBA) into 50‐d old female Sprague Dawley rats, maintained on a standard AIN‐76A diet containing either casein or soy protein. Approximately 120 d following DMBA administration, the animals were sacrificed. All tumors were detected by palpation and at autopsy biopsy specimens were taken for histological grading. The ligand binding capacity, expression, and protein levels of PBRs, their nuclear localization and function, such as nuclear cholesterol uptake and content, were significantly increased in the tumors. However, replacement of casein by soy protein in the diet caused a significant decrease in all of these parameters. These data suggest that soy protein inhibits breast tumor development by decreasing the expression of the tumor‐promoting gene, which encodes PBRs. © 2007 Wiley‐Liss, Inc.</description><subject>9,10-Dimethyl-1,2-benzanthracene - pharmacology</subject><subject>Animals</subject><subject>Benzodiazepinones - metabolism</subject><subject>breast cancer</subject><subject>Carcinogens - pharmacology</subject><subject>Female</subject><subject>Ligands</subject><subject>Mammary Neoplasms, Experimental - chemically induced</subject><subject>Mammary Neoplasms, Experimental - diet therapy</subject><subject>Mammary Neoplasms, Experimental - metabolism</subject><subject>PBRs</subject><subject>Protein Binding</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, GABA-A - metabolism</subject><subject>Receptors, GABA-A - physiology</subject><subject>soy protein</subject><subject>Soybean Proteins - administration &amp; dosage</subject><subject>Soybean Proteins - therapeutic use</subject><subject>Tritium - metabolism</subject><issn>0899-1987</issn><issn>1098-2744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10E1LxDAQBuAgiruugr9AcvTSddK0TXPUqquw6kUR1kNIkylWtx8kFe3-equ76knmMDA8vDAvIYcMpgwgPKnMNASeii0yZiDTIBRRtE3GkEoZMJmKEdnz_gWAMRHDLhkxIXkoIzEmT1lTd65Z0qagLbqyfUanlzTHetXYUq-wLWukDg22XeOCCodjh5bmDrXvqNG1QUfLmjrdeZr31Dc9bV3TYVnvk51CLz0ebPaEPFxe3GdXwfxudp2dzgPDYyGCyGpMZCQLnUAicpamklnLQYKRLA4jzbjVEPPYpFGeWhjGAi-0TawIk0jzCTle5xrXeO-wUK0rK-16xUB99aMqo777GejRmrZv-fDLH9wUMoBgDd7LJfb_Bqmb7Cdw40vf4cev1-5VJYKLWD3eztTibHEeMogV8E8iIH3x</recordid><startdate>200804</startdate><enddate>200804</enddate><creator>Mukhopadhyay, Sutapa</creator><creator>Rajaratnam, Veera</creator><creator>Mukherjee, Shyamali</creator><creator>Das, Salil K.</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></search><sort><creationdate>200804</creationdate><title>Control of peripheral benzodiazepine receptor-mediated breast cancer in rats by soy protein</title><author>Mukhopadhyay, Sutapa ; Rajaratnam, Veera ; Mukherjee, Shyamali ; Das, Salil K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3577-4dae6949fa6067b18891dd3090c91524a13da0535c84b8d0d0dd03fad6d7264a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>9,10-Dimethyl-1,2-benzanthracene - pharmacology</topic><topic>Animals</topic><topic>Benzodiazepinones - metabolism</topic><topic>breast cancer</topic><topic>Carcinogens - pharmacology</topic><topic>Female</topic><topic>Ligands</topic><topic>Mammary Neoplasms, Experimental - chemically induced</topic><topic>Mammary Neoplasms, Experimental - diet therapy</topic><topic>Mammary Neoplasms, Experimental - metabolism</topic><topic>PBRs</topic><topic>Protein Binding</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, GABA-A - metabolism</topic><topic>Receptors, GABA-A - physiology</topic><topic>soy protein</topic><topic>Soybean Proteins - administration &amp; dosage</topic><topic>Soybean Proteins - therapeutic use</topic><topic>Tritium - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukhopadhyay, Sutapa</creatorcontrib><creatorcontrib>Rajaratnam, Veera</creatorcontrib><creatorcontrib>Mukherjee, Shyamali</creatorcontrib><creatorcontrib>Das, Salil K.</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><jtitle>Molecular carcinogenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mukhopadhyay, Sutapa</au><au>Rajaratnam, Veera</au><au>Mukherjee, Shyamali</au><au>Das, Salil K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Control of peripheral benzodiazepine receptor-mediated breast cancer in rats by soy protein</atitle><jtitle>Molecular carcinogenesis</jtitle><addtitle>Mol. Carcinog</addtitle><date>2008-04</date><risdate>2008</risdate><volume>47</volume><issue>4</issue><spage>310</spage><epage>319</epage><pages>310-319</pages><issn>0899-1987</issn><eissn>1098-2744</eissn><abstract>Soy protein is known to have breast tumor suppressing activity. The expression of peripheral benzodiazepine receptors (PBRs), currently renamed as translocator protein (TSPO) and their associated functions, such as nuclear cholesterol uptake and content also have been shown to be increased in breast cancer. Here we investigated whether the breast tumor suppressing effects of soy protein is mediated by down‐regulation of PBR expression and function. Breast tumors were induced by gavage administration of a single dose (80 mg/kg) of dimethylbenz[a]anthracene (DMBA) into 50‐d old female Sprague Dawley rats, maintained on a standard AIN‐76A diet containing either casein or soy protein. Approximately 120 d following DMBA administration, the animals were sacrificed. All tumors were detected by palpation and at autopsy biopsy specimens were taken for histological grading. The ligand binding capacity, expression, and protein levels of PBRs, their nuclear localization and function, such as nuclear cholesterol uptake and content, were significantly increased in the tumors. However, replacement of casein by soy protein in the diet caused a significant decrease in all of these parameters. These data suggest that soy protein inhibits breast tumor development by decreasing the expression of the tumor‐promoting gene, which encodes PBRs. © 2007 Wiley‐Liss, Inc.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17932947</pmid><doi>10.1002/mc.20387</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0899-1987
ispartof Molecular carcinogenesis, 2008-04, Vol.47 (4), p.310-319
issn 0899-1987
1098-2744
language eng
recordid cdi_crossref_primary_10_1002_mc_20387
source MEDLINE; Access via Wiley Online Library
subjects 9,10-Dimethyl-1,2-benzanthracene - pharmacology
Animals
Benzodiazepinones - metabolism
breast cancer
Carcinogens - pharmacology
Female
Ligands
Mammary Neoplasms, Experimental - chemically induced
Mammary Neoplasms, Experimental - diet therapy
Mammary Neoplasms, Experimental - metabolism
PBRs
Protein Binding
Rats
Rats, Sprague-Dawley
Receptors, GABA-A - metabolism
Receptors, GABA-A - physiology
soy protein
Soybean Proteins - administration & dosage
Soybean Proteins - therapeutic use
Tritium - metabolism
title Control of peripheral benzodiazepine receptor-mediated breast cancer in rats by soy protein
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T18%3A09%3A16IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Control%20of%20peripheral%20benzodiazepine%20receptor-mediated%20breast%20cancer%20in%20rats%20by%20soy%20protein&rft.jtitle=Molecular%20carcinogenesis&rft.au=Mukhopadhyay,%20Sutapa&rft.date=2008-04&rft.volume=47&rft.issue=4&rft.spage=310&rft.epage=319&rft.pages=310-319&rft.issn=0899-1987&rft.eissn=1098-2744&rft_id=info:doi/10.1002/mc.20387&rft_dat=%3Cistex_cross%3Eark_67375_WNG_ZBZD2105_0%3C/istex_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/17932947&rfr_iscdi=true