Tocopherols inhibit oxidative and nitrosative stress in estrogen-induced early mammary hyperplasia in ACI rats
Oxidative stress is known to play a key role in estrogen‐induced breast cancer. This study assessed the chemopreventive activity of the naturally occurring γ‐tocopherol‐rich mixture of tocopherols (γ‐TmT) in early stages of estrogen‐induced mammary hyperplasia in ACI rats. ACI rats provide an establ...
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Veröffentlicht in: | Molecular carcinogenesis 2015-09, Vol.54 (9), p.916-925 |
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creator | Das Gupta, Soumyasri So, Jae Young Wall, Brian Wahler, Joseph Smolarek, Amanda K. Sae-tan, Sudathip Soewono, Kelvin Y. Yu, Haixiang Lee, Mao-Jung Thomas, Paul E. Yang, Chung S. Suh, Nanjoo |
description | Oxidative stress is known to play a key role in estrogen‐induced breast cancer. This study assessed the chemopreventive activity of the naturally occurring γ‐tocopherol‐rich mixture of tocopherols (γ‐TmT) in early stages of estrogen‐induced mammary hyperplasia in ACI rats. ACI rats provide an established model of rodent mammary carcinogenesis due to their high sensitivity to estrogen. Female rats were implanted with 9 mg of 17β‐estradiol (E2) in silastic tubings and fed with control or 0.3% γ‐TmT diet for 1, 3, 7, and 14 d. γ‐TmT increased the levels of tocopherols and their metabolites in the serum and mammary glands of the rats. Histological analysis revealed mammary hyperplasia in the E2 treated rats fed with control or γ‐TmT diet. γ‐TmT decreased the levels of E2‐induced nitrosative and oxidative stress markers, nitrotyrosine, and 8‐oxo‐dG, respectively, in the hyperplastic mammary tissues. 8‐Isoprostane, a marker of oxidative stress in the serum, was also reduced by γ‐TmT. Noticeably, γ‐TmT stimulated Nrf2‐dependent antioxidant response in the mammary glands of E2 treated rats, evident from the induced mRNA levels of Nrf2 and its downstream antioxidant enzymes, superoxide dismutase, catalase, and glutathione peroxidase. Therefore, inhibition of nitrosative/oxidative stress through induction of antioxidant response is the primary effect of γ‐TmT in early stages of E2‐induced mammary hyperplasia. Due to its cytoprotective activity, γ‐TmT could be a potential natural agent for the chemoprevention of estrogen‐induced breast cancer. © 2014 Wiley Periodicals, Inc. |
doi_str_mv | 10.1002/mc.22164 |
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This study assessed the chemopreventive activity of the naturally occurring γ‐tocopherol‐rich mixture of tocopherols (γ‐TmT) in early stages of estrogen‐induced mammary hyperplasia in ACI rats. ACI rats provide an established model of rodent mammary carcinogenesis due to their high sensitivity to estrogen. Female rats were implanted with 9 mg of 17β‐estradiol (E2) in silastic tubings and fed with control or 0.3% γ‐TmT diet for 1, 3, 7, and 14 d. γ‐TmT increased the levels of tocopherols and their metabolites in the serum and mammary glands of the rats. Histological analysis revealed mammary hyperplasia in the E2 treated rats fed with control or γ‐TmT diet. γ‐TmT decreased the levels of E2‐induced nitrosative and oxidative stress markers, nitrotyrosine, and 8‐oxo‐dG, respectively, in the hyperplastic mammary tissues. 8‐Isoprostane, a marker of oxidative stress in the serum, was also reduced by γ‐TmT. Noticeably, γ‐TmT stimulated Nrf2‐dependent antioxidant response in the mammary glands of E2 treated rats, evident from the induced mRNA levels of Nrf2 and its downstream antioxidant enzymes, superoxide dismutase, catalase, and glutathione peroxidase. Therefore, inhibition of nitrosative/oxidative stress through induction of antioxidant response is the primary effect of γ‐TmT in early stages of E2‐induced mammary hyperplasia. Due to its cytoprotective activity, γ‐TmT could be a potential natural agent for the chemoprevention of estrogen‐induced breast cancer. © 2014 Wiley Periodicals, Inc.</description><identifier>ISSN: 0899-1987</identifier><identifier>EISSN: 1098-2744</identifier><identifier>DOI: 10.1002/mc.22164</identifier><identifier>PMID: 24782330</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Animals ; Antioxidants - therapeutic use ; Breast cancer ; Breast Diseases - chemically induced ; Breast Diseases - diet therapy ; Breast Diseases - metabolism ; Breast Diseases - pathology ; Dietary Supplements - analysis ; estrogen ; Estrogens ; Female ; Humans ; Hyperplasia - chemically induced ; Hyperplasia - diet therapy ; Hyperplasia - metabolism ; Hyperplasia - pathology ; Mammary Glands, Animal - metabolism ; Mammary Glands, Animal - pathology ; NF-E2-Related Factor 2 - genetics ; Oxidative stress ; Oxidative Stress - drug effects ; Rats ; Rats, Inbred ACI ; RNA, Messenger - genetics ; Rodents ; Tocopherols - therapeutic use ; Tyrosine - analogs & derivatives ; Tyrosine - analysis ; Up-Regulation ; Vitamin E</subject><ispartof>Molecular carcinogenesis, 2015-09, Vol.54 (9), p.916-925</ispartof><rights>2014 Wiley Periodicals, Inc.</rights><rights>2015 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5094-997f1b49881b29c5e1920f74053685d4b31d3fdaaf45de53da4fa9612203d23</citedby></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.22164$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fmc.22164$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24782330$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Das Gupta, Soumyasri</creatorcontrib><creatorcontrib>So, Jae Young</creatorcontrib><creatorcontrib>Wall, Brian</creatorcontrib><creatorcontrib>Wahler, Joseph</creatorcontrib><creatorcontrib>Smolarek, Amanda K.</creatorcontrib><creatorcontrib>Sae-tan, Sudathip</creatorcontrib><creatorcontrib>Soewono, Kelvin Y.</creatorcontrib><creatorcontrib>Yu, Haixiang</creatorcontrib><creatorcontrib>Lee, Mao-Jung</creatorcontrib><creatorcontrib>Thomas, Paul E.</creatorcontrib><creatorcontrib>Yang, Chung S.</creatorcontrib><creatorcontrib>Suh, Nanjoo</creatorcontrib><title>Tocopherols inhibit oxidative and nitrosative stress in estrogen-induced early mammary hyperplasia in ACI rats</title><title>Molecular carcinogenesis</title><addtitle>Mol. Carcinog</addtitle><description>Oxidative stress is known to play a key role in estrogen‐induced breast cancer. This study assessed the chemopreventive activity of the naturally occurring γ‐tocopherol‐rich mixture of tocopherols (γ‐TmT) in early stages of estrogen‐induced mammary hyperplasia in ACI rats. ACI rats provide an established model of rodent mammary carcinogenesis due to their high sensitivity to estrogen. Female rats were implanted with 9 mg of 17β‐estradiol (E2) in silastic tubings and fed with control or 0.3% γ‐TmT diet for 1, 3, 7, and 14 d. γ‐TmT increased the levels of tocopherols and their metabolites in the serum and mammary glands of the rats. Histological analysis revealed mammary hyperplasia in the E2 treated rats fed with control or γ‐TmT diet. γ‐TmT decreased the levels of E2‐induced nitrosative and oxidative stress markers, nitrotyrosine, and 8‐oxo‐dG, respectively, in the hyperplastic mammary tissues. 8‐Isoprostane, a marker of oxidative stress in the serum, was also reduced by γ‐TmT. Noticeably, γ‐TmT stimulated Nrf2‐dependent antioxidant response in the mammary glands of E2 treated rats, evident from the induced mRNA levels of Nrf2 and its downstream antioxidant enzymes, superoxide dismutase, catalase, and glutathione peroxidase. Therefore, inhibition of nitrosative/oxidative stress through induction of antioxidant response is the primary effect of γ‐TmT in early stages of E2‐induced mammary hyperplasia. Due to its cytoprotective activity, γ‐TmT could be a potential natural agent for the chemoprevention of estrogen‐induced breast cancer. © 2014 Wiley Periodicals, Inc.</description><subject>Animals</subject><subject>Antioxidants - therapeutic use</subject><subject>Breast cancer</subject><subject>Breast Diseases - chemically induced</subject><subject>Breast Diseases - diet therapy</subject><subject>Breast Diseases - metabolism</subject><subject>Breast Diseases - pathology</subject><subject>Dietary Supplements - analysis</subject><subject>estrogen</subject><subject>Estrogens</subject><subject>Female</subject><subject>Humans</subject><subject>Hyperplasia - chemically induced</subject><subject>Hyperplasia - diet therapy</subject><subject>Hyperplasia - metabolism</subject><subject>Hyperplasia - pathology</subject><subject>Mammary Glands, Animal - metabolism</subject><subject>Mammary Glands, Animal - pathology</subject><subject>NF-E2-Related Factor 2 - genetics</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Rats</subject><subject>Rats, Inbred ACI</subject><subject>RNA, Messenger - genetics</subject><subject>Rodents</subject><subject>Tocopherols - therapeutic use</subject><subject>Tyrosine - analogs & derivatives</subject><subject>Tyrosine - analysis</subject><subject>Up-Regulation</subject><subject>Vitamin E</subject><issn>0899-1987</issn><issn>1098-2744</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkVtLwzAUx4Mobk7BTyABn6u5dWlehDG8gRfEwR5D2qQu2iY16eb27e2cTn04nHM4P_7nBsAxRmcYIXJeF2eE4CHbAX2MRJYQztgu6KNMiASLjPfAQYyvCGHMU7QPeoTxjFCK-sBNfOGbmQm-itC6mc1tC_3SatXahYHKaehsG3zc5LENJq5BaLrQvxiXWKfnhdHQqFCtYK3qWoUVnK0aE5pKRavW9Gh8C4Nq4yHYK1UVzdG3H4Dnq8vJ-Ca5e7y-HY_ukiJFgiVC8BLnTGQZzokoUoMFQSVnKKXDLNUsp1jTUitVslSblGrFSiWGmBBENaEDcLFRbeZ5bXRhXBtUJZtg17NJr6z8X3F2Jl_8QjImiOiaDMDpt0Dw7_NuVfnq58F1E0vMEWWUss4G4ORvm63-z3U7INkAH7Yyq20dI7n-mqwL-fU1eT_-8r-8ja1ZbnkV3uSQU57K6cO1nE6IwOTmSU7pJ5h_mkI</recordid><startdate>201509</startdate><enddate>201509</enddate><creator>Das Gupta, Soumyasri</creator><creator>So, Jae Young</creator><creator>Wall, Brian</creator><creator>Wahler, Joseph</creator><creator>Smolarek, Amanda K.</creator><creator>Sae-tan, Sudathip</creator><creator>Soewono, Kelvin Y.</creator><creator>Yu, Haixiang</creator><creator>Lee, Mao-Jung</creator><creator>Thomas, Paul E.</creator><creator>Yang, Chung S.</creator><creator>Suh, Nanjoo</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7TM</scope><scope>7TO</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>201509</creationdate><title>Tocopherols inhibit oxidative and nitrosative stress in estrogen-induced early mammary hyperplasia in ACI rats</title><author>Das Gupta, Soumyasri ; So, Jae Young ; Wall, Brian ; Wahler, Joseph ; Smolarek, Amanda K. ; Sae-tan, Sudathip ; Soewono, Kelvin Y. ; Yu, Haixiang ; Lee, Mao-Jung ; Thomas, Paul E. ; Yang, Chung S. ; Suh, Nanjoo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5094-997f1b49881b29c5e1920f74053685d4b31d3fdaaf45de53da4fa9612203d23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Animals</topic><topic>Antioxidants - therapeutic use</topic><topic>Breast cancer</topic><topic>Breast Diseases - chemically induced</topic><topic>Breast Diseases - diet therapy</topic><topic>Breast Diseases - metabolism</topic><topic>Breast Diseases - pathology</topic><topic>Dietary Supplements - analysis</topic><topic>estrogen</topic><topic>Estrogens</topic><topic>Female</topic><topic>Humans</topic><topic>Hyperplasia - chemically induced</topic><topic>Hyperplasia - diet therapy</topic><topic>Hyperplasia - metabolism</topic><topic>Hyperplasia - pathology</topic><topic>Mammary Glands, Animal - metabolism</topic><topic>Mammary Glands, Animal - pathology</topic><topic>NF-E2-Related Factor 2 - genetics</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Rats</topic><topic>Rats, Inbred ACI</topic><topic>RNA, Messenger - genetics</topic><topic>Rodents</topic><topic>Tocopherols - therapeutic use</topic><topic>Tyrosine - analogs & derivatives</topic><topic>Tyrosine - analysis</topic><topic>Up-Regulation</topic><topic>Vitamin E</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Das Gupta, Soumyasri</creatorcontrib><creatorcontrib>So, Jae Young</creatorcontrib><creatorcontrib>Wall, Brian</creatorcontrib><creatorcontrib>Wahler, Joseph</creatorcontrib><creatorcontrib>Smolarek, Amanda K.</creatorcontrib><creatorcontrib>Sae-tan, Sudathip</creatorcontrib><creatorcontrib>Soewono, Kelvin Y.</creatorcontrib><creatorcontrib>Yu, Haixiang</creatorcontrib><creatorcontrib>Lee, Mao-Jung</creatorcontrib><creatorcontrib>Thomas, Paul E.</creatorcontrib><creatorcontrib>Yang, Chung S.</creatorcontrib><creatorcontrib>Suh, Nanjoo</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Molecular carcinogenesis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Das Gupta, Soumyasri</au><au>So, Jae Young</au><au>Wall, Brian</au><au>Wahler, Joseph</au><au>Smolarek, Amanda K.</au><au>Sae-tan, Sudathip</au><au>Soewono, Kelvin Y.</au><au>Yu, Haixiang</au><au>Lee, Mao-Jung</au><au>Thomas, Paul E.</au><au>Yang, Chung S.</au><au>Suh, Nanjoo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tocopherols inhibit oxidative and nitrosative stress in estrogen-induced early mammary hyperplasia in ACI rats</atitle><jtitle>Molecular carcinogenesis</jtitle><addtitle>Mol. Carcinog</addtitle><date>2015-09</date><risdate>2015</risdate><volume>54</volume><issue>9</issue><spage>916</spage><epage>925</epage><pages>916-925</pages><issn>0899-1987</issn><eissn>1098-2744</eissn><abstract>Oxidative stress is known to play a key role in estrogen‐induced breast cancer. This study assessed the chemopreventive activity of the naturally occurring γ‐tocopherol‐rich mixture of tocopherols (γ‐TmT) in early stages of estrogen‐induced mammary hyperplasia in ACI rats. ACI rats provide an established model of rodent mammary carcinogenesis due to their high sensitivity to estrogen. Female rats were implanted with 9 mg of 17β‐estradiol (E2) in silastic tubings and fed with control or 0.3% γ‐TmT diet for 1, 3, 7, and 14 d. γ‐TmT increased the levels of tocopherols and their metabolites in the serum and mammary glands of the rats. Histological analysis revealed mammary hyperplasia in the E2 treated rats fed with control or γ‐TmT diet. γ‐TmT decreased the levels of E2‐induced nitrosative and oxidative stress markers, nitrotyrosine, and 8‐oxo‐dG, respectively, in the hyperplastic mammary tissues. 8‐Isoprostane, a marker of oxidative stress in the serum, was also reduced by γ‐TmT. Noticeably, γ‐TmT stimulated Nrf2‐dependent antioxidant response in the mammary glands of E2 treated rats, evident from the induced mRNA levels of Nrf2 and its downstream antioxidant enzymes, superoxide dismutase, catalase, and glutathione peroxidase. Therefore, inhibition of nitrosative/oxidative stress through induction of antioxidant response is the primary effect of γ‐TmT in early stages of E2‐induced mammary hyperplasia. Due to its cytoprotective activity, γ‐TmT could be a potential natural agent for the chemoprevention of estrogen‐induced breast cancer. © 2014 Wiley Periodicals, Inc.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>24782330</pmid><doi>10.1002/mc.22164</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Antioxidants - therapeutic use Breast cancer Breast Diseases - chemically induced Breast Diseases - diet therapy Breast Diseases - metabolism Breast Diseases - pathology Dietary Supplements - analysis estrogen Estrogens Female Humans Hyperplasia - chemically induced Hyperplasia - diet therapy Hyperplasia - metabolism Hyperplasia - pathology Mammary Glands, Animal - metabolism Mammary Glands, Animal - pathology NF-E2-Related Factor 2 - genetics Oxidative stress Oxidative Stress - drug effects Rats Rats, Inbred ACI RNA, Messenger - genetics Rodents Tocopherols - therapeutic use Tyrosine - analogs & derivatives Tyrosine - analysis Up-Regulation Vitamin E |
title | Tocopherols inhibit oxidative and nitrosative stress in estrogen-induced early mammary hyperplasia in ACI rats |
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