Studies on Estrogenic Activities of Food Additives with Human Breast Cancer MCF-7 Cells and Mechanism of Estrogenicity by BHA and OPP
Estrogenic activities of more than 90 chemicals including food additives, foodstuffs of plant origin, and some chemicals, which could be orally ingested, were examined by assaying estrogen receptor (ER)-dependent proliferation of MCF-7 cells. Among 66 food additives, 17 compounds stimulated the prol...
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Veröffentlicht in: | YAKUGAKU ZASSHI 2003/06/01, Vol.123(6), pp.443-452 |
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description | Estrogenic activities of more than 90 chemicals including food additives, foodstuffs of plant origin, and some chemicals, which could be orally ingested, were examined by assaying estrogen receptor (ER)-dependent proliferation of MCF-7 cells. Among 66 food additives, 17 compounds stimulated the proliferation, but their concentrations giving maximal cell yield were higher than that of 17β-estradiol and their estrogenic activities were weak. Flavonoids had relatively strong estrogenic activities. In the assay of ER competitive binding to human ERα and ERβ in vitro, the antioxidant t-butylhydroxyanisole (BHA) had the capacity to compete with 17β-estradiol, while the capacity of o-phenyl phenol (OPP) was too small to calculate. Both BHA and OPP induced a decrease in gene expression of ERα and an increase in that of progesterone receptor in a time-dependent manner. These effects were similar to that of 17β-estradiol, a though much higher concentrations were required for these compounds than 17β-estradiol. These results may suggest that we should be careful not to ingest excessive food additives. |
doi_str_mv | 10.1248/yakushi.123.443 |
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Among 66 food additives, 17 compounds stimulated the proliferation, but their concentrations giving maximal cell yield were higher than that of 17β-estradiol and their estrogenic activities were weak. Flavonoids had relatively strong estrogenic activities. In the assay of ER competitive binding to human ERα and ERβ in vitro, the antioxidant t-butylhydroxyanisole (BHA) had the capacity to compete with 17β-estradiol, while the capacity of o-phenyl phenol (OPP) was too small to calculate. Both BHA and OPP induced a decrease in gene expression of ERα and an increase in that of progesterone receptor in a time-dependent manner. These effects were similar to that of 17β-estradiol, a though much higher concentrations were required for these compounds than 17β-estradiol. These results may suggest that we should be careful not to ingest excessive food additives.</description><identifier>ISSN: 0031-6903</identifier><identifier>EISSN: 1347-5231</identifier><identifier>DOI: 10.1248/yakushi.123.443</identifier><identifier>PMID: 12822488</identifier><language>jpn</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>Antioxidants - adverse effects ; Antioxidants - metabolism ; BHA ; Binding, Competitive ; Biphenyl Compounds - adverse effects ; Biphenyl Compounds - metabolism ; Breast Neoplasms - metabolism ; Breast Neoplasms - pathology ; Butylated Hydroxyanisole - adverse effects ; Butylated Hydroxyanisole - metabolism ; Cell Division - drug effects ; Dose-Response Relationship, Drug ; Estradiol - metabolism ; Estradiol - pharmacology ; estrogen ; estrogen receptor ; Estrogen Receptor alpha ; Female ; Food Additives - adverse effects ; food-additive ; Fungicides, Industrial - adverse effects ; Fungicides, Industrial - metabolism ; Gene Expression - drug effects ; Humans ; MCF-7 ; OPP ; Receptors, Estrogen - genetics ; Receptors, Estrogen - metabolism ; Receptors, Estrogen - physiology ; Time Factors ; Tumor Cells, Cultured</subject><ispartof>YAKUGAKU ZASSHI, 2003/06/01, Vol.123(6), pp.443-452</ispartof><rights>2003 by the PHARMACEUTICAL SOCIETY OF JAPAN</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,1881,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12822488$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>OKUBO, Tomoko</creatorcontrib><creatorcontrib>KANO, Itsu</creatorcontrib><title>Studies on Estrogenic Activities of Food Additives with Human Breast Cancer MCF-7 Cells and Mechanism of Estrogenicity by BHA and OPP</title><title>YAKUGAKU ZASSHI</title><addtitle>YAKUGAKU ZASSHI</addtitle><description>Estrogenic activities of more than 90 chemicals including food additives, foodstuffs of plant origin, and some chemicals, which could be orally ingested, were examined by assaying estrogen receptor (ER)-dependent proliferation of MCF-7 cells. Among 66 food additives, 17 compounds stimulated the proliferation, but their concentrations giving maximal cell yield were higher than that of 17β-estradiol and their estrogenic activities were weak. Flavonoids had relatively strong estrogenic activities. In the assay of ER competitive binding to human ERα and ERβ in vitro, the antioxidant t-butylhydroxyanisole (BHA) had the capacity to compete with 17β-estradiol, while the capacity of o-phenyl phenol (OPP) was too small to calculate. Both BHA and OPP induced a decrease in gene expression of ERα and an increase in that of progesterone receptor in a time-dependent manner. These effects were similar to that of 17β-estradiol, a though much higher concentrations were required for these compounds than 17β-estradiol. These results may suggest that we should be careful not to ingest excessive food additives.</description><subject>Antioxidants - adverse effects</subject><subject>Antioxidants - metabolism</subject><subject>BHA</subject><subject>Binding, Competitive</subject><subject>Biphenyl Compounds - adverse effects</subject><subject>Biphenyl Compounds - metabolism</subject><subject>Breast Neoplasms - metabolism</subject><subject>Breast Neoplasms - pathology</subject><subject>Butylated Hydroxyanisole - adverse effects</subject><subject>Butylated Hydroxyanisole - metabolism</subject><subject>Cell Division - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Estradiol - metabolism</subject><subject>Estradiol - pharmacology</subject><subject>estrogen</subject><subject>estrogen receptor</subject><subject>Estrogen Receptor alpha</subject><subject>Female</subject><subject>Food Additives - adverse effects</subject><subject>food-additive</subject><subject>Fungicides, Industrial - adverse effects</subject><subject>Fungicides, Industrial - metabolism</subject><subject>Gene Expression - drug effects</subject><subject>Humans</subject><subject>MCF-7</subject><subject>OPP</subject><subject>Receptors, Estrogen - genetics</subject><subject>Receptors, Estrogen - metabolism</subject><subject>Receptors, Estrogen - physiology</subject><subject>Time Factors</subject><subject>Tumor Cells, Cultured</subject><issn>0031-6903</issn><issn>1347-5231</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFUMtuwjAQtKpWBVHOvVX-gVC_8vAxRFAqgUBqe44cZwOmJKDYUPEB_e-6QOkedjWzsyPtIPRIyYAykTwf1eferowHfCAEv0FdykUchIzTW9QlhNMgkoR3UN9aUxDCfIU0uUcdyhLmHZIu-n5z-9KAxdsGj6xrt0tojMapduZg3GlR4fF2W-K0LD1x8MyXcSs82deqwcMWlHU4U42GFs-ycRDjDDYbi1VT4hnolWqMrX9N_t2NO-LiiIeT9KSaLxYP6K5SGwv9y-yhj_HoPZsE0_nLa5ZOgzWLpAuEFERHEEsBsogop6RIKh7FTLOEMiYZ0VXkoSICyrIAIkOQsaZahgkkmvMeejr77vZFDWW-a02t2mP-l4cXjM6CtXVqCVeBap3RG8gvkfsDnkeX7qO_7v2_bQ4N_wGRNHxZ</recordid><startdate>20030601</startdate><enddate>20030601</enddate><creator>OKUBO, Tomoko</creator><creator>KANO, Itsu</creator><general>The Pharmaceutical Society of Japan</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20030601</creationdate><title>Studies on Estrogenic Activities of Food Additives with Human Breast Cancer MCF-7 Cells and Mechanism of Estrogenicity by BHA and OPP</title><author>OKUBO, Tomoko ; KANO, Itsu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j269t-4940c6e794e9b61310b8f3672c28122920cf6672a04eddbe095e97c1c958e8c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>jpn</language><creationdate>2003</creationdate><topic>Antioxidants - adverse effects</topic><topic>Antioxidants - metabolism</topic><topic>BHA</topic><topic>Binding, Competitive</topic><topic>Biphenyl Compounds - adverse effects</topic><topic>Biphenyl Compounds - metabolism</topic><topic>Breast Neoplasms - metabolism</topic><topic>Breast Neoplasms - pathology</topic><topic>Butylated Hydroxyanisole - adverse effects</topic><topic>Butylated Hydroxyanisole - metabolism</topic><topic>Cell Division - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Estradiol - metabolism</topic><topic>Estradiol - pharmacology</topic><topic>estrogen</topic><topic>estrogen receptor</topic><topic>Estrogen Receptor alpha</topic><topic>Female</topic><topic>Food Additives - adverse effects</topic><topic>food-additive</topic><topic>Fungicides, Industrial - adverse effects</topic><topic>Fungicides, Industrial - metabolism</topic><topic>Gene Expression - drug effects</topic><topic>Humans</topic><topic>MCF-7</topic><topic>OPP</topic><topic>Receptors, Estrogen - genetics</topic><topic>Receptors, Estrogen - metabolism</topic><topic>Receptors, Estrogen - physiology</topic><topic>Time Factors</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>OKUBO, Tomoko</creatorcontrib><creatorcontrib>KANO, Itsu</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>YAKUGAKU ZASSHI</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>OKUBO, Tomoko</au><au>KANO, Itsu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies on Estrogenic Activities of Food Additives with Human Breast Cancer MCF-7 Cells and Mechanism of Estrogenicity by BHA and OPP</atitle><jtitle>YAKUGAKU ZASSHI</jtitle><addtitle>YAKUGAKU ZASSHI</addtitle><date>2003-06-01</date><risdate>2003</risdate><volume>123</volume><issue>6</issue><spage>443</spage><epage>452</epage><pages>443-452</pages><issn>0031-6903</issn><eissn>1347-5231</eissn><abstract>Estrogenic activities of more than 90 chemicals including food additives, foodstuffs of plant origin, and some chemicals, which could be orally ingested, were examined by assaying estrogen receptor (ER)-dependent proliferation of MCF-7 cells. Among 66 food additives, 17 compounds stimulated the proliferation, but their concentrations giving maximal cell yield were higher than that of 17β-estradiol and their estrogenic activities were weak. Flavonoids had relatively strong estrogenic activities. In the assay of ER competitive binding to human ERα and ERβ in vitro, the antioxidant t-butylhydroxyanisole (BHA) had the capacity to compete with 17β-estradiol, while the capacity of o-phenyl phenol (OPP) was too small to calculate. Both BHA and OPP induced a decrease in gene expression of ERα and an increase in that of progesterone receptor in a time-dependent manner. These effects were similar to that of 17β-estradiol, a though much higher concentrations were required for these compounds than 17β-estradiol. These results may suggest that we should be careful not to ingest excessive food additives.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>12822488</pmid><doi>10.1248/yakushi.123.443</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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source | MEDLINE; J-STAGE (Japan Science & Technology Information Aggregator, Electronic) Freely Available Titles - Japanese; Alma/SFX Local Collection |
subjects | Antioxidants - adverse effects Antioxidants - metabolism BHA Binding, Competitive Biphenyl Compounds - adverse effects Biphenyl Compounds - metabolism Breast Neoplasms - metabolism Breast Neoplasms - pathology Butylated Hydroxyanisole - adverse effects Butylated Hydroxyanisole - metabolism Cell Division - drug effects Dose-Response Relationship, Drug Estradiol - metabolism Estradiol - pharmacology estrogen estrogen receptor Estrogen Receptor alpha Female Food Additives - adverse effects food-additive Fungicides, Industrial - adverse effects Fungicides, Industrial - metabolism Gene Expression - drug effects Humans MCF-7 OPP Receptors, Estrogen - genetics Receptors, Estrogen - metabolism Receptors, Estrogen - physiology Time Factors Tumor Cells, Cultured |
title | Studies on Estrogenic Activities of Food Additives with Human Breast Cancer MCF-7 Cells and Mechanism of Estrogenicity by BHA and OPP |
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