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...
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Veröffentlicht in: | Molecular carcinogenesis 2008-04, Vol.47 (4), p.310-319 |
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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. |
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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 & 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 & 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 & 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> |
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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 |
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