Role of high-fat diet on the effect of pioglitazone and melatonin in a rat model of breast cancer
The risk of cancer may be modulated by drugs with pleiotropic effects and diet has been implicated in the efficacy of treatment. The oncopreventive effects of the antidiabetic drug pioglitazone (PIO) and the anti-insomnia drug melatonin (MT), in vivo, have been proven before, but using a standard-ty...
Gespeichert in:
Veröffentlicht in: | European journal of cancer prevention 2016-09, Vol.25 (5), p.395-403 |
---|---|
Hauptverfasser: | , , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 403 |
---|---|
container_issue | 5 |
container_start_page | 395 |
container_title | European journal of cancer prevention |
container_volume | 25 |
creator | Bojková, Bianka Orendáš, Peter Kajo, Karol Kubatka, Peter Výbohová, Desanka Bálentová, Sona Kružliak, Peter Zulli, Anthony Demecková, Vlasta Péč, Martin Adamkov, Marián |
description | The risk of cancer may be modulated by drugs with pleiotropic effects and diet has been implicated in the efficacy of treatment. The oncopreventive effects of the antidiabetic drug pioglitazone (PIO) and the anti-insomnia drug melatonin (MT), in vivo, have been proven before, but using a standard-type diet. This study evaluated the impact of a high-fat diet on their efficacy in chemically induced mammary carcinogenesis in Sprague–Dawley rats. Mammary tumours were induced by N-methyl-N-nitrosourea (50 mg/kg, intraperitoneal, on the 41st postnatal day). PIO and MT administration was initiated 11 days before the carcinogen application and lasted until the termination of the experiment at 16 weeks. PIO was administered in a diet (10% fat) at a concentration of 100 ppm and MT was administered in tap water (20 mg/l). PIO, MT and the combination did not significantly alter the basic tumour growth parameters. However, histopathology showed a decrease in the high-grade/low-grade tumour ratio, particularly in animals that received combined treatment (P |
doi_str_mv | 10.1097/CEJ.0000000000000195 |
format | Article |
fullrecord | <record><control><sourceid>jstor_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1097_CEJ_0000000000000195</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><jstor_id>48504498</jstor_id><sourcerecordid>48504498</sourcerecordid><originalsourceid>FETCH-LOGICAL-c329t-54584afa0c49c1e1b01ea6dbc656af02c8eeef4040ab51d85a21520e053555093</originalsourceid><addsrcrecordid>eNpdkN1Kw0AQRhdRbK2-gcq-QOpssptkL6XUPwqC6HWYbGbblCRbdtcLfXpTqiIOA3PxnW8uDmOXAuYCdHGzWD7N4e8IrY7YVMgiS1QB-phNQSudlGlRTthZCNsRKTKRn7JJmmcSQBVThi-uI-4s37TrTWIx8qalyN3A44Y4WUsm7uNd69ZdG_HTDcRxaHhPHUY3tAMfF7kfm71rqNvDtScMkRscDPlzdmKxC3TxfWfs7W75unhIVs_3j4vbVWKyVMdESVVKtAhGaiNI1CAI86Y2ucrRQmpKIrISJGCtRFMqTIVKgUBlSinQ2YzJw1_jXQiebLXzbY_-oxJQ7Y1Vo7Hqv7Gxdn2o7d7rnprf0o-iEbg6ANsQnf_NZalASl1mX0vSb5s</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Role of high-fat diet on the effect of pioglitazone and melatonin in a rat model of breast cancer</title><source>MEDLINE</source><source>JSTOR Archive Collection A-Z Listing</source><creator>Bojková, Bianka ; Orendáš, Peter ; Kajo, Karol ; Kubatka, Peter ; Výbohová, Desanka ; Bálentová, Sona ; Kružliak, Peter ; Zulli, Anthony ; Demecková, Vlasta ; Péč, Martin ; Adamkov, Marián</creator><creatorcontrib>Bojková, Bianka ; Orendáš, Peter ; Kajo, Karol ; Kubatka, Peter ; Výbohová, Desanka ; Bálentová, Sona ; Kružliak, Peter ; Zulli, Anthony ; Demecková, Vlasta ; Péč, Martin ; Adamkov, Marián</creatorcontrib><description>The risk of cancer may be modulated by drugs with pleiotropic effects and diet has been implicated in the efficacy of treatment. The oncopreventive effects of the antidiabetic drug pioglitazone (PIO) and the anti-insomnia drug melatonin (MT), in vivo, have been proven before, but using a standard-type diet. This study evaluated the impact of a high-fat diet on their efficacy in chemically induced mammary carcinogenesis in Sprague–Dawley rats. Mammary tumours were induced by N-methyl-N-nitrosourea (50 mg/kg, intraperitoneal, on the 41st postnatal day). PIO and MT administration was initiated 11 days before the carcinogen application and lasted until the termination of the experiment at 16 weeks. PIO was administered in a diet (10% fat) at a concentration of 100 ppm and MT was administered in tap water (20 mg/l). PIO, MT and the combination did not significantly alter the basic tumour growth parameters. However, histopathology showed a decrease in the high-grade/low-grade tumour ratio, particularly in animals that received combined treatment (P<0.01). Semiquantitative immunohistochemistry indicated the proapoptotic effect of chemoprevention, particularly in the drug combination group (P<0.01), but no changes in tumour cell proliferation and angiogenesis were recorded. Results were evaluated by one-way analysis of variance or the Mann–Whitney U-test, respectively. PIO and MT, alone or in combination, administered to rats fed a high-fat diet reduced the proportion of high-grade tumours and promoted apoptosis in an in-vivo breast cancer model, although it did not suppress tumour growth. The impact of high dietary fat content on the chemopreventive efficacy of these and other substances should be considered in human studies.</description><identifier>ISSN: 0959-8278</identifier><identifier>EISSN: 1473-5709</identifier><identifier>DOI: 10.1097/CEJ.0000000000000195</identifier><identifier>PMID: 26340057</identifier><language>eng</language><publisher>England: Lippincott Williams & Wilkins, a business of Wolters Kluwer Health</publisher><subject>Animals ; Antioxidants - pharmacology ; Carcinogens - toxicity ; Diet, High-Fat - adverse effects ; Disease Models, Animal ; Drug Therapy, Combination ; Female ; Hypoglycemic Agents - pharmacology ; Mammary Neoplasms, Experimental - drug therapy ; Mammary Neoplasms, Experimental - etiology ; Mammary Neoplasms, Experimental - pathology ; Melatonin - pharmacology ; Methylnitrosourea - toxicity ; Rats ; Rats, Sprague-Dawley ; Research paper ; Thiazolidinediones - pharmacology</subject><ispartof>European journal of cancer prevention, 2016-09, Vol.25 (5), p.395-403</ispartof><rights>Copyright © 2016 Wolters Kluwer Health, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c329t-54584afa0c49c1e1b01ea6dbc656af02c8eeef4040ab51d85a21520e053555093</citedby><cites>FETCH-LOGICAL-c329t-54584afa0c49c1e1b01ea6dbc656af02c8eeef4040ab51d85a21520e053555093</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/48504498$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/48504498$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,27923,27924,58016,58249</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26340057$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bojková, Bianka</creatorcontrib><creatorcontrib>Orendáš, Peter</creatorcontrib><creatorcontrib>Kajo, Karol</creatorcontrib><creatorcontrib>Kubatka, Peter</creatorcontrib><creatorcontrib>Výbohová, Desanka</creatorcontrib><creatorcontrib>Bálentová, Sona</creatorcontrib><creatorcontrib>Kružliak, Peter</creatorcontrib><creatorcontrib>Zulli, Anthony</creatorcontrib><creatorcontrib>Demecková, Vlasta</creatorcontrib><creatorcontrib>Péč, Martin</creatorcontrib><creatorcontrib>Adamkov, Marián</creatorcontrib><title>Role of high-fat diet on the effect of pioglitazone and melatonin in a rat model of breast cancer</title><title>European journal of cancer prevention</title><addtitle>Eur J Cancer Prev</addtitle><description>The risk of cancer may be modulated by drugs with pleiotropic effects and diet has been implicated in the efficacy of treatment. The oncopreventive effects of the antidiabetic drug pioglitazone (PIO) and the anti-insomnia drug melatonin (MT), in vivo, have been proven before, but using a standard-type diet. This study evaluated the impact of a high-fat diet on their efficacy in chemically induced mammary carcinogenesis in Sprague–Dawley rats. Mammary tumours were induced by N-methyl-N-nitrosourea (50 mg/kg, intraperitoneal, on the 41st postnatal day). PIO and MT administration was initiated 11 days before the carcinogen application and lasted until the termination of the experiment at 16 weeks. PIO was administered in a diet (10% fat) at a concentration of 100 ppm and MT was administered in tap water (20 mg/l). PIO, MT and the combination did not significantly alter the basic tumour growth parameters. However, histopathology showed a decrease in the high-grade/low-grade tumour ratio, particularly in animals that received combined treatment (P<0.01). Semiquantitative immunohistochemistry indicated the proapoptotic effect of chemoprevention, particularly in the drug combination group (P<0.01), but no changes in tumour cell proliferation and angiogenesis were recorded. Results were evaluated by one-way analysis of variance or the Mann–Whitney U-test, respectively. PIO and MT, alone or in combination, administered to rats fed a high-fat diet reduced the proportion of high-grade tumours and promoted apoptosis in an in-vivo breast cancer model, although it did not suppress tumour growth. The impact of high dietary fat content on the chemopreventive efficacy of these and other substances should be considered in human studies.</description><subject>Animals</subject><subject>Antioxidants - pharmacology</subject><subject>Carcinogens - toxicity</subject><subject>Diet, High-Fat - adverse effects</subject><subject>Disease Models, Animal</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Hypoglycemic Agents - pharmacology</subject><subject>Mammary Neoplasms, Experimental - drug therapy</subject><subject>Mammary Neoplasms, Experimental - etiology</subject><subject>Mammary Neoplasms, Experimental - pathology</subject><subject>Melatonin - pharmacology</subject><subject>Methylnitrosourea - toxicity</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Research paper</subject><subject>Thiazolidinediones - pharmacology</subject><issn>0959-8278</issn><issn>1473-5709</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkN1Kw0AQRhdRbK2-gcq-QOpssptkL6XUPwqC6HWYbGbblCRbdtcLfXpTqiIOA3PxnW8uDmOXAuYCdHGzWD7N4e8IrY7YVMgiS1QB-phNQSudlGlRTthZCNsRKTKRn7JJmmcSQBVThi-uI-4s37TrTWIx8qalyN3A44Y4WUsm7uNd69ZdG_HTDcRxaHhPHUY3tAMfF7kfm71rqNvDtScMkRscDPlzdmKxC3TxfWfs7W75unhIVs_3j4vbVWKyVMdESVVKtAhGaiNI1CAI86Y2ucrRQmpKIrISJGCtRFMqTIVKgUBlSinQ2YzJw1_jXQiebLXzbY_-oxJQ7Y1Vo7Hqv7Gxdn2o7d7rnprf0o-iEbg6ANsQnf_NZalASl1mX0vSb5s</recordid><startdate>20160901</startdate><enddate>20160901</enddate><creator>Bojková, Bianka</creator><creator>Orendáš, Peter</creator><creator>Kajo, Karol</creator><creator>Kubatka, Peter</creator><creator>Výbohová, Desanka</creator><creator>Bálentová, Sona</creator><creator>Kružliak, Peter</creator><creator>Zulli, Anthony</creator><creator>Demecková, Vlasta</creator><creator>Péč, Martin</creator><creator>Adamkov, Marián</creator><general>Lippincott Williams & Wilkins, a business of Wolters Kluwer Health</general><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>20160901</creationdate><title>Role of high-fat diet on the effect of pioglitazone and melatonin in a rat model of breast cancer</title><author>Bojková, Bianka ; Orendáš, Peter ; Kajo, Karol ; Kubatka, Peter ; Výbohová, Desanka ; Bálentová, Sona ; Kružliak, Peter ; Zulli, Anthony ; Demecková, Vlasta ; Péč, Martin ; Adamkov, Marián</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c329t-54584afa0c49c1e1b01ea6dbc656af02c8eeef4040ab51d85a21520e053555093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Antioxidants - pharmacology</topic><topic>Carcinogens - toxicity</topic><topic>Diet, High-Fat - adverse effects</topic><topic>Disease Models, Animal</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Hypoglycemic Agents - pharmacology</topic><topic>Mammary Neoplasms, Experimental - drug therapy</topic><topic>Mammary Neoplasms, Experimental - etiology</topic><topic>Mammary Neoplasms, Experimental - pathology</topic><topic>Melatonin - pharmacology</topic><topic>Methylnitrosourea - toxicity</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Research paper</topic><topic>Thiazolidinediones - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bojková, Bianka</creatorcontrib><creatorcontrib>Orendáš, Peter</creatorcontrib><creatorcontrib>Kajo, Karol</creatorcontrib><creatorcontrib>Kubatka, Peter</creatorcontrib><creatorcontrib>Výbohová, Desanka</creatorcontrib><creatorcontrib>Bálentová, Sona</creatorcontrib><creatorcontrib>Kružliak, Peter</creatorcontrib><creatorcontrib>Zulli, Anthony</creatorcontrib><creatorcontrib>Demecková, Vlasta</creatorcontrib><creatorcontrib>Péč, Martin</creatorcontrib><creatorcontrib>Adamkov, Marián</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>European journal of cancer prevention</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bojková, Bianka</au><au>Orendáš, Peter</au><au>Kajo, Karol</au><au>Kubatka, Peter</au><au>Výbohová, Desanka</au><au>Bálentová, Sona</au><au>Kružliak, Peter</au><au>Zulli, Anthony</au><au>Demecková, Vlasta</au><au>Péč, Martin</au><au>Adamkov, Marián</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of high-fat diet on the effect of pioglitazone and melatonin in a rat model of breast cancer</atitle><jtitle>European journal of cancer prevention</jtitle><addtitle>Eur J Cancer Prev</addtitle><date>2016-09-01</date><risdate>2016</risdate><volume>25</volume><issue>5</issue><spage>395</spage><epage>403</epage><pages>395-403</pages><issn>0959-8278</issn><eissn>1473-5709</eissn><abstract>The risk of cancer may be modulated by drugs with pleiotropic effects and diet has been implicated in the efficacy of treatment. The oncopreventive effects of the antidiabetic drug pioglitazone (PIO) and the anti-insomnia drug melatonin (MT), in vivo, have been proven before, but using a standard-type diet. This study evaluated the impact of a high-fat diet on their efficacy in chemically induced mammary carcinogenesis in Sprague–Dawley rats. Mammary tumours were induced by N-methyl-N-nitrosourea (50 mg/kg, intraperitoneal, on the 41st postnatal day). PIO and MT administration was initiated 11 days before the carcinogen application and lasted until the termination of the experiment at 16 weeks. PIO was administered in a diet (10% fat) at a concentration of 100 ppm and MT was administered in tap water (20 mg/l). PIO, MT and the combination did not significantly alter the basic tumour growth parameters. However, histopathology showed a decrease in the high-grade/low-grade tumour ratio, particularly in animals that received combined treatment (P<0.01). Semiquantitative immunohistochemistry indicated the proapoptotic effect of chemoprevention, particularly in the drug combination group (P<0.01), but no changes in tumour cell proliferation and angiogenesis were recorded. Results were evaluated by one-way analysis of variance or the Mann–Whitney U-test, respectively. PIO and MT, alone or in combination, administered to rats fed a high-fat diet reduced the proportion of high-grade tumours and promoted apoptosis in an in-vivo breast cancer model, although it did not suppress tumour growth. The impact of high dietary fat content on the chemopreventive efficacy of these and other substances should be considered in human studies.</abstract><cop>England</cop><pub>Lippincott Williams & Wilkins, a business of Wolters Kluwer Health</pub><pmid>26340057</pmid><doi>10.1097/CEJ.0000000000000195</doi><tpages>9</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0959-8278 |
ispartof | European journal of cancer prevention, 2016-09, Vol.25 (5), p.395-403 |
issn | 0959-8278 1473-5709 |
language | eng |
recordid | cdi_crossref_primary_10_1097_CEJ_0000000000000195 |
source | MEDLINE; JSTOR Archive Collection A-Z Listing |
subjects | Animals Antioxidants - pharmacology Carcinogens - toxicity Diet, High-Fat - adverse effects Disease Models, Animal Drug Therapy, Combination Female Hypoglycemic Agents - pharmacology Mammary Neoplasms, Experimental - drug therapy Mammary Neoplasms, Experimental - etiology Mammary Neoplasms, Experimental - pathology Melatonin - pharmacology Methylnitrosourea - toxicity Rats Rats, Sprague-Dawley Research paper Thiazolidinediones - pharmacology |
title | Role of high-fat diet on the effect of pioglitazone and melatonin in a rat model of breast cancer |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T01%3A12%3A18IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-jstor_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Role%20of%20high-fat%20diet%20on%20the%20effect%20of%20pioglitazone%20and%20melatonin%20in%20a%20rat%20model%20of%20breast%20cancer&rft.jtitle=European%20journal%20of%20cancer%20prevention&rft.au=Bojkov%C3%A1,%20Bianka&rft.date=2016-09-01&rft.volume=25&rft.issue=5&rft.spage=395&rft.epage=403&rft.pages=395-403&rft.issn=0959-8278&rft.eissn=1473-5709&rft_id=info:doi/10.1097/CEJ.0000000000000195&rft_dat=%3Cjstor_cross%3E48504498%3C/jstor_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/26340057&rft_jstor_id=48504498&rfr_iscdi=true |