Maternal Dioxin Exposure Combined with a Diet High in Fat Increases Mammary Cancer Incidence in Mice
Background: Results from previous studies have suggested that breast cancer risk correlates with total lifetime exposure to estrogens and that early-life 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure or diets high in fat can also increase cancer risk. Objectives: Because both TCDD and diet aff...
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Veröffentlicht in: | Environmental health perspectives 2010-05, Vol.118 (5), p.596-601 |
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description | Background: Results from previous studies have suggested that breast cancer risk correlates with total lifetime exposure to estrogens and that early-life 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure or diets high in fat can also increase cancer risk. Objectives: Because both TCDD and diet affect the estrogen pathway, we examined how TCDD and a high-fat diet (HFD) interact to alter breast cancer susceptibility. Methods: We exposed pregnant female FVB/NJ mice (12.5 days postcoitus) to 1 μg/kg TCDD or vehicle; at parturition, the dams were randomly assigned to a low-fat diet (LFD) or a high-fat diet (HFD). Female offspring were maintained on the same diets after weaning and were exposed to 7,12-dimethylbenz[a]anthracene on postnatal days (PNDs) 35, 49, and 63 to initiate mammary tumors. A second cohort of females was treated identically until PND35 or PND49, when mammary gland morphology was examined, or PND50, when mammary gland mRNA was analyzed. Results: We found that maternal TCDD exposure doubled mammary tumor incidence only in mice fed the HFD. Among HFD-fed mice, maternal TCDD exposure caused rapid mammary development with increased Cyp1b1 (cytochrome P450 1B1) expression and decreased Comt (catechol-O-methyltransferase) expression in mammary tissue. Maternal TCDD exposure also increased mammary tumor Cyp1b1 expression. Conclusions: Our data suggest that the HFD increases sensitivity to maternal TCDD exposure, resulting in increased breast cancer incidence, by changing metabolism capability. These results provide a mechanism to explain epidemiological data linking early-life TCDD exposure and diets high in fat to increased risk for breast cancer in humans. |
doi_str_mv | 10.1289/ehp.0901047 |
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Objectives: Because both TCDD and diet affect the estrogen pathway, we examined how TCDD and a high-fat diet (HFD) interact to alter breast cancer susceptibility. Methods: We exposed pregnant female FVB/NJ mice (12.5 days postcoitus) to 1 μg/kg TCDD or vehicle; at parturition, the dams were randomly assigned to a low-fat diet (LFD) or a high-fat diet (HFD). Female offspring were maintained on the same diets after weaning and were exposed to 7,12-dimethylbenz[a]anthracene on postnatal days (PNDs) 35, 49, and 63 to initiate mammary tumors. A second cohort of females was treated identically until PND35 or PND49, when mammary gland morphology was examined, or PND50, when mammary gland mRNA was analyzed. Results: We found that maternal TCDD exposure doubled mammary tumor incidence only in mice fed the HFD. Among HFD-fed mice, maternal TCDD exposure caused rapid mammary development with increased Cyp1b1 (cytochrome P450 1B1) expression and decreased Comt (catechol-O-methyltransferase) expression in mammary tissue. Maternal TCDD exposure also increased mammary tumor Cyp1b1 expression. Conclusions: Our data suggest that the HFD increases sensitivity to maternal TCDD exposure, resulting in increased breast cancer incidence, by changing metabolism capability. These results provide a mechanism to explain epidemiological data linking early-life TCDD exposure and diets high in fat to increased risk for breast cancer in humans.</description><identifier>ISSN: 0091-6765</identifier><identifier>EISSN: 1552-9924</identifier><identifier>DOI: 10.1289/ehp.0901047</identifier><identifier>PMID: 20435547</identifier><identifier>CODEN: EVHPAZ</identifier><language>eng</language><publisher>Research Triangle Park, NC: National Institute of Environmental Health Sciences</publisher><subject>Animals ; Aryl Hydrocarbon Hydroxylases - genetics ; Biological and medical sciences ; Breast cancer ; Cancer ; Carcinogenesis ; Catechol O-Methyltransferase - genetics ; Cocarcinogenesis ; Cytochrome P-450 CYP1B1 ; Diagnosis ; Dietary Fats - administration & dosage ; Dietary Fats - adverse effects ; Dioxin ; Environment. Living conditions ; Environmental Pollutants - administration & dosage ; Environmental Pollutants - toxicity ; Estrogens ; Estrogens, Non-Steroidal - administration & dosage ; Estrogens, Non-Steroidal - toxicity ; Female ; Gene Expression - drug effects ; Gynecology. Andrology. Obstetrics ; Health aspects ; Humans ; Ketogenic diet ; Lesions ; Mammary gland diseases ; Mammary glands ; Mammary Neoplasms, Experimental - etiology ; Mammary Neoplasms, Experimental - genetics ; Mammary Neoplasms, Experimental - pathology ; Medical sciences ; Mice ; Polychlorinated Dibenzodioxins - administration & dosage ; Polychlorinated Dibenzodioxins - toxicity ; Pregnancy ; Prenatal Exposure Delayed Effects - etiology ; Public health. Hygiene ; Public health. Hygiene-occupational medicine ; Rats ; Risk Factors ; Toxicology ; Tumors ; Vehicles</subject><ispartof>Environmental health perspectives, 2010-05, Vol.118 (5), p.596-601</ispartof><rights>2015 INIST-CNRS</rights><rights>COPYRIGHT 2010 National Institute of Environmental Health Sciences</rights><rights>Copyright National Institute of Environmental Health Sciences May 2010</rights><rights>2010</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c695t-b62ddb7a9cf37d3266ef324cf2dffc880d12de83f9b68f07b7e4a74980ffac333</citedby><cites>FETCH-LOGICAL-c695t-b62ddb7a9cf37d3266ef324cf2dffc880d12de83f9b68f07b7e4a74980ffac333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/25653878$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/25653878$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,864,885,27922,27923,53789,53791,58015,58248</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=22701103$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20435547$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>La Merrill, Michele</creatorcontrib><creatorcontrib>Harper, Rachel</creatorcontrib><creatorcontrib>Birnbaum, Linda S.</creatorcontrib><creatorcontrib>Cardiff, Robert D.</creatorcontrib><creatorcontrib>Threadgill, David W.</creatorcontrib><title>Maternal Dioxin Exposure Combined with a Diet High in Fat Increases Mammary Cancer Incidence in Mice</title><title>Environmental health perspectives</title><addtitle>Environ Health Perspect</addtitle><description>Background: Results from previous studies have suggested that breast cancer risk correlates with total lifetime exposure to estrogens and that early-life 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure or diets high in fat can also increase cancer risk. Objectives: Because both TCDD and diet affect the estrogen pathway, we examined how TCDD and a high-fat diet (HFD) interact to alter breast cancer susceptibility. Methods: We exposed pregnant female FVB/NJ mice (12.5 days postcoitus) to 1 μg/kg TCDD or vehicle; at parturition, the dams were randomly assigned to a low-fat diet (LFD) or a high-fat diet (HFD). Female offspring were maintained on the same diets after weaning and were exposed to 7,12-dimethylbenz[a]anthracene on postnatal days (PNDs) 35, 49, and 63 to initiate mammary tumors. A second cohort of females was treated identically until PND35 or PND49, when mammary gland morphology was examined, or PND50, when mammary gland mRNA was analyzed. Results: We found that maternal TCDD exposure doubled mammary tumor incidence only in mice fed the HFD. Among HFD-fed mice, maternal TCDD exposure caused rapid mammary development with increased Cyp1b1 (cytochrome P450 1B1) expression and decreased Comt (catechol-O-methyltransferase) expression in mammary tissue. Maternal TCDD exposure also increased mammary tumor Cyp1b1 expression. Conclusions: Our data suggest that the HFD increases sensitivity to maternal TCDD exposure, resulting in increased breast cancer incidence, by changing metabolism capability. These results provide a mechanism to explain epidemiological data linking early-life TCDD exposure and diets high in fat to increased risk for breast cancer in humans.</description><subject>Animals</subject><subject>Aryl Hydrocarbon Hydroxylases - genetics</subject><subject>Biological and medical sciences</subject><subject>Breast cancer</subject><subject>Cancer</subject><subject>Carcinogenesis</subject><subject>Catechol O-Methyltransferase - genetics</subject><subject>Cocarcinogenesis</subject><subject>Cytochrome P-450 CYP1B1</subject><subject>Diagnosis</subject><subject>Dietary Fats - administration & dosage</subject><subject>Dietary Fats - adverse effects</subject><subject>Dioxin</subject><subject>Environment. Living conditions</subject><subject>Environmental Pollutants - administration & dosage</subject><subject>Environmental Pollutants - toxicity</subject><subject>Estrogens</subject><subject>Estrogens, Non-Steroidal - administration & dosage</subject><subject>Estrogens, Non-Steroidal - toxicity</subject><subject>Female</subject><subject>Gene Expression - drug effects</subject><subject>Gynecology. Andrology. Obstetrics</subject><subject>Health aspects</subject><subject>Humans</subject><subject>Ketogenic diet</subject><subject>Lesions</subject><subject>Mammary gland diseases</subject><subject>Mammary glands</subject><subject>Mammary Neoplasms, Experimental - etiology</subject><subject>Mammary Neoplasms, Experimental - genetics</subject><subject>Mammary Neoplasms, Experimental - pathology</subject><subject>Medical sciences</subject><subject>Mice</subject><subject>Polychlorinated Dibenzodioxins - administration & dosage</subject><subject>Polychlorinated Dibenzodioxins - toxicity</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects - etiology</subject><subject>Public health. Hygiene</subject><subject>Public health. Hygiene-occupational medicine</subject><subject>Rats</subject><subject>Risk Factors</subject><subject>Toxicology</subject><subject>Tumors</subject><subject>Vehicles</subject><issn>0091-6765</issn><issn>1552-9924</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqN0s9v0zAUB_AIgVgZnDiDoiFACKU4TmInF6SpbKzSqkn8ulqO89y4SuxiO1v573Fo2VbUA8ohUd7Hz0_2N4qep2ia4rL6AO16iiqUopw-iCZpUeCkqnD-MJogVKUJoaQ4ip44t0IIpSUhj6MjjPKsKHI6iZoF92A17-JPymyUjs82a-MGC_HM9LXS0MQ3yrcxD3Xw8YVatnFQ59zHcy0scAcuXvC-5_ZXPONagB0LqoHwOcqFEvA0eiR55-DZ7n0cfT8_-za7SC6vPs9np5eJIFXhk5rgpqkpr4TMaJNhQkBmOBcSN1KKskRNihsoM1nVpJSI1hRyTvOqRFJykWXZcfRx23c91D00ArS3vGNrq8bxmOGK7Ve0atnSXDMcjoVQHBq83TWw5ucAzrNeOQFdxzWYwTGa56Qqsz_y5B-5MsN4jo5hjAkO0-cBvdqiJe-AKS1N2FWMLdkpxjSn4zUElRxQS9AQRjQapAq_9_z0gA9PA70SBxe821sQjIeNX_LBOTb_-uX_7dWPffvmnm2Bd751phu8Mtrtw_dbKKxxzoK8vZIUsTHDLGSY7TIc9Mv7t3hr_4Y2gNc7wJ3gnbQhdsrdOUxRmqIxDi-2buW8sXf1ghRZScvsN_B4_tg</recordid><startdate>20100501</startdate><enddate>20100501</enddate><creator>La Merrill, Michele</creator><creator>Harper, Rachel</creator><creator>Birnbaum, Linda S.</creator><creator>Cardiff, Robert D.</creator><creator>Threadgill, David W.</creator><general>National Institute of Environmental Health Sciences</general><general>US Department of Health and Human Services</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>IOV</scope><scope>ISR</scope><scope>3V.</scope><scope>4T-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FE</scope><scope>8FG</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AEUYN</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>L6V</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7S</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>S0X</scope><scope>7ST</scope><scope>7U7</scope><scope>C1K</scope><scope>SOI</scope><scope>5PM</scope></search><sort><creationdate>20100501</creationdate><title>Maternal Dioxin Exposure Combined with a Diet High in Fat Increases Mammary Cancer Incidence in Mice</title><author>La Merrill, Michele ; Harper, Rachel ; Birnbaum, Linda S. ; Cardiff, Robert D. ; Threadgill, David W.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c695t-b62ddb7a9cf37d3266ef324cf2dffc880d12de83f9b68f07b7e4a74980ffac333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Animals</topic><topic>Aryl Hydrocarbon Hydroxylases - genetics</topic><topic>Biological and medical sciences</topic><topic>Breast cancer</topic><topic>Cancer</topic><topic>Carcinogenesis</topic><topic>Catechol O-Methyltransferase - genetics</topic><topic>Cocarcinogenesis</topic><topic>Cytochrome P-450 CYP1B1</topic><topic>Diagnosis</topic><topic>Dietary Fats - administration & dosage</topic><topic>Dietary Fats - adverse effects</topic><topic>Dioxin</topic><topic>Environment. Living conditions</topic><topic>Environmental Pollutants - administration & dosage</topic><topic>Environmental Pollutants - toxicity</topic><topic>Estrogens</topic><topic>Estrogens, Non-Steroidal - administration & dosage</topic><topic>Estrogens, Non-Steroidal - toxicity</topic><topic>Female</topic><topic>Gene Expression - drug effects</topic><topic>Gynecology. Andrology. Obstetrics</topic><topic>Health aspects</topic><topic>Humans</topic><topic>Ketogenic diet</topic><topic>Lesions</topic><topic>Mammary gland diseases</topic><topic>Mammary glands</topic><topic>Mammary Neoplasms, Experimental - etiology</topic><topic>Mammary Neoplasms, Experimental - genetics</topic><topic>Mammary Neoplasms, Experimental - pathology</topic><topic>Medical sciences</topic><topic>Mice</topic><topic>Polychlorinated Dibenzodioxins - administration & dosage</topic><topic>Polychlorinated Dibenzodioxins - toxicity</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects - etiology</topic><topic>Public health. Hygiene</topic><topic>Public health. Hygiene-occupational medicine</topic><topic>Rats</topic><topic>Risk Factors</topic><topic>Toxicology</topic><topic>Tumors</topic><topic>Vehicles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>La Merrill, Michele</creatorcontrib><creatorcontrib>Harper, Rachel</creatorcontrib><creatorcontrib>Birnbaum, Linda S.</creatorcontrib><creatorcontrib>Cardiff, Robert D.</creatorcontrib><creatorcontrib>Threadgill, David W.</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>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>Materials Science & Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest One Sustainability</collection><collection>ProQuest Central UK/Ireland</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Technology Collection</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>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Engineering Collection</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Engineering Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Environmental 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>Engineering Collection</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>Environment Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Environmental health perspectives</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>La Merrill, Michele</au><au>Harper, Rachel</au><au>Birnbaum, Linda S.</au><au>Cardiff, Robert D.</au><au>Threadgill, David W.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Maternal Dioxin Exposure Combined with a Diet High in Fat Increases Mammary Cancer Incidence in Mice</atitle><jtitle>Environmental health perspectives</jtitle><addtitle>Environ Health Perspect</addtitle><date>2010-05-01</date><risdate>2010</risdate><volume>118</volume><issue>5</issue><spage>596</spage><epage>601</epage><pages>596-601</pages><issn>0091-6765</issn><eissn>1552-9924</eissn><coden>EVHPAZ</coden><abstract>Background: Results from previous studies have suggested that breast cancer risk correlates with total lifetime exposure to estrogens and that early-life 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) exposure or diets high in fat can also increase cancer risk. Objectives: Because both TCDD and diet affect the estrogen pathway, we examined how TCDD and a high-fat diet (HFD) interact to alter breast cancer susceptibility. Methods: We exposed pregnant female FVB/NJ mice (12.5 days postcoitus) to 1 μg/kg TCDD or vehicle; at parturition, the dams were randomly assigned to a low-fat diet (LFD) or a high-fat diet (HFD). Female offspring were maintained on the same diets after weaning and were exposed to 7,12-dimethylbenz[a]anthracene on postnatal days (PNDs) 35, 49, and 63 to initiate mammary tumors. A second cohort of females was treated identically until PND35 or PND49, when mammary gland morphology was examined, or PND50, when mammary gland mRNA was analyzed. Results: We found that maternal TCDD exposure doubled mammary tumor incidence only in mice fed the HFD. Among HFD-fed mice, maternal TCDD exposure caused rapid mammary development with increased Cyp1b1 (cytochrome P450 1B1) expression and decreased Comt (catechol-O-methyltransferase) expression in mammary tissue. Maternal TCDD exposure also increased mammary tumor Cyp1b1 expression. Conclusions: Our data suggest that the HFD increases sensitivity to maternal TCDD exposure, resulting in increased breast cancer incidence, by changing metabolism capability. These results provide a mechanism to explain epidemiological data linking early-life TCDD exposure and diets high in fat to increased risk for breast cancer in humans.</abstract><cop>Research Triangle Park, NC</cop><pub>National Institute of Environmental Health Sciences</pub><pmid>20435547</pmid><doi>10.1289/ehp.0901047</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Aryl Hydrocarbon Hydroxylases - genetics Biological and medical sciences Breast cancer Cancer Carcinogenesis Catechol O-Methyltransferase - genetics Cocarcinogenesis Cytochrome P-450 CYP1B1 Diagnosis Dietary Fats - administration & dosage Dietary Fats - adverse effects Dioxin Environment. Living conditions Environmental Pollutants - administration & dosage Environmental Pollutants - toxicity Estrogens Estrogens, Non-Steroidal - administration & dosage Estrogens, Non-Steroidal - toxicity Female Gene Expression - drug effects Gynecology. Andrology. Obstetrics Health aspects Humans Ketogenic diet Lesions Mammary gland diseases Mammary glands Mammary Neoplasms, Experimental - etiology Mammary Neoplasms, Experimental - genetics Mammary Neoplasms, Experimental - pathology Medical sciences Mice Polychlorinated Dibenzodioxins - administration & dosage Polychlorinated Dibenzodioxins - toxicity Pregnancy Prenatal Exposure Delayed Effects - etiology Public health. Hygiene Public health. Hygiene-occupational medicine Rats Risk Factors Toxicology Tumors Vehicles |
title | Maternal Dioxin Exposure Combined with a Diet High in Fat Increases Mammary Cancer Incidence in Mice |
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