Species, Interindividual, and Tissue Specificity in Endocrine Signaling
The activity of endocrine-active agents exhibits specificity at many levels. Differential responsiveness to these agents has been observed between different species and extends to interindividual differences within a species and between different tissues as well. In cases where they have been identi...
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Veröffentlicht in: | Environmental health perspectives 1999-08, Vol.107 (suppl 4), p.619-624 |
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description | The activity of endocrine-active agents exhibits specificity at many levels. Differential responsiveness to these agents has been observed between different species and extends to interindividual differences within a species and between different tissues as well. In cases where they have been identified, the biologic and molecular mechanisms underlying this specificity are quite diverse. Determinants of species specificity include differences that exist in receptor binding, gene transcription, and cellular responses to endocrine-active compounds between species. Interindividual differences in responsiveness may be determined at the level of genetic polymorphisms in hormone-metabolizing enzymes, hormone receptors, and in those genes that are transactivated by these receptors, as well as during changing windows of susceptibility that occur as a function of age, such as prenatal and postmenopausal exposures. Extrinsic factors such as diet can also impact individual susceptibility to endocrine-active agents. Tissue-specific determinants of susceptibility are well documented, but little is known regarding the mechanisms underlying these different responses. Differences in the expression of accessory proteins for steroid hormone receptors and different patterns of receptor expression, estrogen receptor α and estrogen receptor β for example, may contribute to tissue specificity, as may differences in the pattern of expression of other genes such as hormone-metabolizing enzymes. The use of animal model systems and development of appropriate mathematical models has the potential to yield additional valuable information for elucidating the role of these determinants of specificity at low-dose exposures and for improved risk assessments for the adverse health effects of endocrine-active compounds. |
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Ansar ; Brown, Terry ; Ho, Shuk-Mei ; Hodges, Leslie ; Lucier, George ; Russo, Jose ; Weigel, Nancy ; Weise, Tom ; Vandenbergh, John</creator><creatorcontrib>Walker, Cheryl ; Ahmed, S. Ansar ; Brown, Terry ; Ho, Shuk-Mei ; Hodges, Leslie ; Lucier, George ; Russo, Jose ; Weigel, Nancy ; Weise, Tom ; Vandenbergh, John</creatorcontrib><description>The activity of endocrine-active agents exhibits specificity at many levels. Differential responsiveness to these agents has been observed between different species and extends to interindividual differences within a species and between different tissues as well. In cases where they have been identified, the biologic and molecular mechanisms underlying this specificity are quite diverse. Determinants of species specificity include differences that exist in receptor binding, gene transcription, and cellular responses to endocrine-active compounds between species. Interindividual differences in responsiveness may be determined at the level of genetic polymorphisms in hormone-metabolizing enzymes, hormone receptors, and in those genes that are transactivated by these receptors, as well as during changing windows of susceptibility that occur as a function of age, such as prenatal and postmenopausal exposures. Extrinsic factors such as diet can also impact individual susceptibility to endocrine-active agents. Tissue-specific determinants of susceptibility are well documented, but little is known regarding the mechanisms underlying these different responses. Differences in the expression of accessory proteins for steroid hormone receptors and different patterns of receptor expression, estrogen receptor α and estrogen receptor β for example, may contribute to tissue specificity, as may differences in the pattern of expression of other genes such as hormone-metabolizing enzymes. The use of animal model systems and development of appropriate mathematical models has the potential to yield additional valuable information for elucidating the role of these determinants of specificity at low-dose exposures and for improved risk assessments for the adverse health effects of endocrine-active compounds.</description><identifier>ISSN: 0091-6765</identifier><identifier>EISSN: 1552-9924</identifier><identifier>DOI: 10.1289/ehp.99107s4619</identifier><identifier>PMID: 10421772</identifier><language>eng</language><publisher>United States: National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare</publisher><subject>Age Factors ; Animal models ; Animals ; Breast cancer ; Characterizing the Effects of Endocrine Disruptors on Human Health at Environmental Exposure Levels: Monograph Based on Papers Developed at the Workshop on Characterizing the Effects of Endocrine Disruptors on Human Health at Environmental Exposure Levels Held 11-13 May 1998 in Raleigh, North Carolina ; Disease Models, Animal ; Dose response relationship ; Dose-Response Relationship, Drug ; Endocrine disruptors ; Endocrine System - drug effects ; Endocrine System - physiology ; Environmental Pollutants - adverse effects ; Estrogens ; Genes ; genetic polymorphism ; Hormones ; Humans ; Menopause ; Models, Theoretical ; Prostate ; Rats ; Receptors ; Receptors, Estrogen - drug effects ; Receptors, Estrogen - physiology ; Signal Transduction ; Species Specificity ; Transcription, Genetic ; Xenobiotics - adverse effects</subject><ispartof>Environmental health perspectives, 1999-08, Vol.107 (suppl 4), p.619-624</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c446t-3a603acd358733b03ca35bd85a5605913aa3911d907b228d8927f105da4b02753</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/3434554$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/3434554$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,864,885,27924,27925,53791,53793,58017,58250</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10421772$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Walker, Cheryl</creatorcontrib><creatorcontrib>Ahmed, S. Ansar</creatorcontrib><creatorcontrib>Brown, Terry</creatorcontrib><creatorcontrib>Ho, Shuk-Mei</creatorcontrib><creatorcontrib>Hodges, Leslie</creatorcontrib><creatorcontrib>Lucier, George</creatorcontrib><creatorcontrib>Russo, Jose</creatorcontrib><creatorcontrib>Weigel, Nancy</creatorcontrib><creatorcontrib>Weise, Tom</creatorcontrib><creatorcontrib>Vandenbergh, John</creatorcontrib><title>Species, Interindividual, and Tissue Specificity in Endocrine Signaling</title><title>Environmental health perspectives</title><addtitle>Environ Health Perspect</addtitle><description>The activity of endocrine-active agents exhibits specificity at many levels. Differential responsiveness to these agents has been observed between different species and extends to interindividual differences within a species and between different tissues as well. In cases where they have been identified, the biologic and molecular mechanisms underlying this specificity are quite diverse. Determinants of species specificity include differences that exist in receptor binding, gene transcription, and cellular responses to endocrine-active compounds between species. Interindividual differences in responsiveness may be determined at the level of genetic polymorphisms in hormone-metabolizing enzymes, hormone receptors, and in those genes that are transactivated by these receptors, as well as during changing windows of susceptibility that occur as a function of age, such as prenatal and postmenopausal exposures. Extrinsic factors such as diet can also impact individual susceptibility to endocrine-active agents. Tissue-specific determinants of susceptibility are well documented, but little is known regarding the mechanisms underlying these different responses. Differences in the expression of accessory proteins for steroid hormone receptors and different patterns of receptor expression, estrogen receptor α and estrogen receptor β for example, may contribute to tissue specificity, as may differences in the pattern of expression of other genes such as hormone-metabolizing enzymes. The use of animal model systems and development of appropriate mathematical models has the potential to yield additional valuable information for elucidating the role of these determinants of specificity at low-dose exposures and for improved risk assessments for the adverse health effects of endocrine-active compounds.</description><subject>Age Factors</subject><subject>Animal models</subject><subject>Animals</subject><subject>Breast cancer</subject><subject>Characterizing the Effects of Endocrine Disruptors on Human Health at Environmental Exposure Levels: Monograph Based on Papers Developed at the Workshop on Characterizing the Effects of Endocrine Disruptors on Human Health at Environmental Exposure Levels Held 11-13 May 1998 in Raleigh, North Carolina</subject><subject>Disease Models, Animal</subject><subject>Dose response relationship</subject><subject>Dose-Response Relationship, Drug</subject><subject>Endocrine disruptors</subject><subject>Endocrine System - drug effects</subject><subject>Endocrine System - physiology</subject><subject>Environmental Pollutants - adverse effects</subject><subject>Estrogens</subject><subject>Genes</subject><subject>genetic polymorphism</subject><subject>Hormones</subject><subject>Humans</subject><subject>Menopause</subject><subject>Models, Theoretical</subject><subject>Prostate</subject><subject>Rats</subject><subject>Receptors</subject><subject>Receptors, Estrogen - drug effects</subject><subject>Receptors, Estrogen - physiology</subject><subject>Signal Transduction</subject><subject>Species Specificity</subject><subject>Transcription, Genetic</subject><subject>Xenobiotics - adverse effects</subject><issn>0091-6765</issn><issn>1552-9924</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1999</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkD1PwzAQhi0EglJYGVEGxNSU83e8ICEEpVIlBspsObZbjFKnxAkS_56UVlCmG97nnju9CF1gGGNSqBv_th4rhUEmJrA6QAPMOcmVIuwQDQAUzoUU_ASdpvQOALgQ4hidYGAES0kGaPKy9jb4NMqmsfVNiC58BteZapSZ6LJ5SKnz2Q-0CDa0X1mI2UN0te3ZPgjLaKoQl2foaGGq5M93c4heHx_m90_57Hkyvb-b5ZYx0ebUCKDGOsoLSWkJ1BrKS1dwwwVwhakxVGHsFMiSkMIVisgFBu4MK4FITofodutdd-XKO-tj25hKr5uwMs2Xrk3Q_5MY3vSy_tSYC8lhI7jeCZr6o_Op1auQrK8qE33dJY0lLagkqgfHW9A2dUqNX_wewaA33eu-e_3Xfb9wuf_aHr4tuweutsB7autmX0coSE0ZZZwz-g2_ZIun</recordid><startdate>19990801</startdate><enddate>19990801</enddate><creator>Walker, Cheryl</creator><creator>Ahmed, S. Ansar</creator><creator>Brown, Terry</creator><creator>Ho, Shuk-Mei</creator><creator>Hodges, Leslie</creator><creator>Lucier, George</creator><creator>Russo, Jose</creator><creator>Weigel, Nancy</creator><creator>Weise, Tom</creator><creator>Vandenbergh, John</creator><general>National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare</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><scope>7U7</scope><scope>C1K</scope><scope>5PM</scope></search><sort><creationdate>19990801</creationdate><title>Species, Interindividual, and Tissue Specificity in Endocrine Signaling</title><author>Walker, Cheryl ; Ahmed, S. Ansar ; Brown, Terry ; Ho, Shuk-Mei ; Hodges, Leslie ; Lucier, George ; Russo, Jose ; Weigel, Nancy ; Weise, Tom ; Vandenbergh, John</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c446t-3a603acd358733b03ca35bd85a5605913aa3911d907b228d8927f105da4b02753</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1999</creationdate><topic>Age Factors</topic><topic>Animal models</topic><topic>Animals</topic><topic>Breast cancer</topic><topic>Characterizing the Effects of Endocrine Disruptors on Human Health at Environmental Exposure Levels: Monograph Based on Papers Developed at the Workshop on Characterizing the Effects of Endocrine Disruptors on Human Health at Environmental Exposure Levels Held 11-13 May 1998 in Raleigh, North Carolina</topic><topic>Disease Models, Animal</topic><topic>Dose response relationship</topic><topic>Dose-Response Relationship, Drug</topic><topic>Endocrine disruptors</topic><topic>Endocrine System - drug effects</topic><topic>Endocrine System - physiology</topic><topic>Environmental Pollutants - adverse effects</topic><topic>Estrogens</topic><topic>Genes</topic><topic>genetic polymorphism</topic><topic>Hormones</topic><topic>Humans</topic><topic>Menopause</topic><topic>Models, Theoretical</topic><topic>Prostate</topic><topic>Rats</topic><topic>Receptors</topic><topic>Receptors, Estrogen - drug effects</topic><topic>Receptors, Estrogen - physiology</topic><topic>Signal Transduction</topic><topic>Species Specificity</topic><topic>Transcription, Genetic</topic><topic>Xenobiotics - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Walker, Cheryl</creatorcontrib><creatorcontrib>Ahmed, S. Ansar</creatorcontrib><creatorcontrib>Brown, Terry</creatorcontrib><creatorcontrib>Ho, Shuk-Mei</creatorcontrib><creatorcontrib>Hodges, Leslie</creatorcontrib><creatorcontrib>Lucier, George</creatorcontrib><creatorcontrib>Russo, Jose</creatorcontrib><creatorcontrib>Weigel, Nancy</creatorcontrib><creatorcontrib>Weise, Tom</creatorcontrib><creatorcontrib>Vandenbergh, John</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</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>Walker, Cheryl</au><au>Ahmed, S. Ansar</au><au>Brown, Terry</au><au>Ho, Shuk-Mei</au><au>Hodges, Leslie</au><au>Lucier, George</au><au>Russo, Jose</au><au>Weigel, Nancy</au><au>Weise, Tom</au><au>Vandenbergh, John</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Species, Interindividual, and Tissue Specificity in Endocrine Signaling</atitle><jtitle>Environmental health perspectives</jtitle><addtitle>Environ Health Perspect</addtitle><date>1999-08-01</date><risdate>1999</risdate><volume>107</volume><issue>suppl 4</issue><spage>619</spage><epage>624</epage><pages>619-624</pages><issn>0091-6765</issn><eissn>1552-9924</eissn><abstract>The activity of endocrine-active agents exhibits specificity at many levels. Differential responsiveness to these agents has been observed between different species and extends to interindividual differences within a species and between different tissues as well. In cases where they have been identified, the biologic and molecular mechanisms underlying this specificity are quite diverse. Determinants of species specificity include differences that exist in receptor binding, gene transcription, and cellular responses to endocrine-active compounds between species. Interindividual differences in responsiveness may be determined at the level of genetic polymorphisms in hormone-metabolizing enzymes, hormone receptors, and in those genes that are transactivated by these receptors, as well as during changing windows of susceptibility that occur as a function of age, such as prenatal and postmenopausal exposures. Extrinsic factors such as diet can also impact individual susceptibility to endocrine-active agents. Tissue-specific determinants of susceptibility are well documented, but little is known regarding the mechanisms underlying these different responses. Differences in the expression of accessory proteins for steroid hormone receptors and different patterns of receptor expression, estrogen receptor α and estrogen receptor β for example, may contribute to tissue specificity, as may differences in the pattern of expression of other genes such as hormone-metabolizing enzymes. The use of animal model systems and development of appropriate mathematical models has the potential to yield additional valuable information for elucidating the role of these determinants of specificity at low-dose exposures and for improved risk assessments for the adverse health effects of endocrine-active compounds.</abstract><cop>United States</cop><pub>National Institute of Environmental Health Sciences. National Institutes of Health. Department of Health, Education and Welfare</pub><pmid>10421772</pmid><doi>10.1289/ehp.99107s4619</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Age Factors Animal models Animals Breast cancer Characterizing the Effects of Endocrine Disruptors on Human Health at Environmental Exposure Levels: Monograph Based on Papers Developed at the Workshop on Characterizing the Effects of Endocrine Disruptors on Human Health at Environmental Exposure Levels Held 11-13 May 1998 in Raleigh, North Carolina Disease Models, Animal Dose response relationship Dose-Response Relationship, Drug Endocrine disruptors Endocrine System - drug effects Endocrine System - physiology Environmental Pollutants - adverse effects Estrogens Genes genetic polymorphism Hormones Humans Menopause Models, Theoretical Prostate Rats Receptors Receptors, Estrogen - drug effects Receptors, Estrogen - physiology Signal Transduction Species Specificity Transcription, Genetic Xenobiotics - adverse effects |
title | Species, Interindividual, and Tissue Specificity in Endocrine Signaling |
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