Epigenetic Marks of Xenoestrogen Exposure
Epigenetic Marks of Xenoestrogen Exposure
批准号:
7941819
负责人:
DAVID J WAXMAN
金额:
$41.06万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-09-28 至 2012-07-31
关键词:
AddressAdultAdverse effectsAreaChemicalsChromatinCoupledDataDefectDetectionDevelopmentDiethylstilbestrolDiseaseDoseEconomicsEmbryoEndocrineEndocrine DisruptorsEnvironmental EstrogenEnvironmental ExposureEpigenetic ProcessExpenditureExposure toFemaleFertilityFunctional disorderFundingGene ExpressionGenesGenomicsGoalsHealthHumanIncidenceIndividualKnowledgeLaboratory ResearchLeadLesionLifeLinkMammalsMicroarray AnalysisModelingMolecularMusNaturePerinatalPerinatal ExposurePreventionRecoveryResearchSelective Estrogen Receptor ModulatorsStimulusTechnologyTestingToxic effectToxicologyUterine CancerUterusbasebisphenol Achromatin immunoprecipitationcritical periodenvironmental chemicalepigenomicsestrogenic activityexposed human populationfetalgenome-wideimprintin uteroinsightmouse modelneoplasticpostnatalpublic health relevancereproductiveresponsexenoestrogen
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): This application addresses broad Challenge Area (08) Genomics and specific Challenge Topic 08-ES-104, Identification of Alterations in Epigenetic Marks Related to Environmental Exposures. Environmental exposure to foreign chemicals with estrogenic activities is widespread and is proposed to impact adversely on human health. Exposure to these xenoestrogens and other endocrine-disrupting chemicals has been associated with a variety of developmental and reproductive abnormalities, with humans and other species being hypersensitive to endocrine-active compounds during critical periods of embryonic, fetal and early postnatal life. The overall goal of this project is to investigate the hypothesis that perinatal exposure to xenoestrogens induces epigenetic marks associated with permanent changes in expression of key genes controlling female reproductive tract development, which are, in turn, linked to the observed reproductive tract abnormalities and increased incidence of uterine cancer. It is proposed that each xenoestrogen has a unique epigenetic signature as a result of its unique activity as a selective estrogen receptor modulator. These hypotheses will be tested using in utero mouse models of exposure to the xenoestrogens diethylstilbestrol and bisphenol-A. Diethylstilbestrol is a potent xenoestrogen linked to major reproductive tract developmental abnormalities in mouse models and in exposed humans, while bisphenol-A is a weak xenoestrogen that induces more modest reproductive toxicities in the mouse; the consequences of human exposure to the latter chemical are not definitively established. Discovery of the epigenetic signatures that are common, as well as those that are unique, to each xenoestrogen will help elucidate the reproductive toxicology associated with each chemical. These studies will provide important new insight into the mechanisms through which endocrine-active environmental chemicals induce reproductive toxicities, and may, ultimately, lead to new strategies for detection and prevention of adverse effects in exposed individuals. The significance of the studies proposed is major, both in terms of the new scientific knowledge that is expected to result, and for the potential impact on the large number of individuals that are exposed to environmental xenoestrogens. The economic stimulatory impact is also expected to be major, advancing Recovery Act goals through the direct hiring of research staff to support the needs of this project and via the positive economic stimulus that will result from the expenditure of laboratory research supplies funds.
PUBLIC HEALTH RELEVANCE: This project investigates the actions of environmental chemicals that exert reproductive toxicities, with special emphasis on environmental estrogens that induce female reproductive tract toxicities in humans and other exposed mammals. The studies that are proposed will provide important new insight into the mechanisms through which endocrine-active environmental chemicals induce reproductive toxicities, and may, ultimately, lead to new strategies for detection and prevention of adverse effects in exposed individuals.
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会议论文
Xenobiotic-responsive hepatic long non-coding RNAs
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批准号:10711162
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项目类别:
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资助金额:$3.49万
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财政年份:2022
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负责人:DAVID J WAXMAN
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依托单位:
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批准号:9897015
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项目类别:
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资助金额:$49.11万
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财政年份:2019
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负责人:DAVID J WAXMAN
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依托单位:
Growth Hormone Regulation of Sex Differences in Liver Metabolism
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批准号:10626011
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项目类别:
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资助金额:$49.63万
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财政年份:2019
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负责人:DAVID J WAXMAN
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依托单位:
Growth Hormone Regulation of Sex Differences in Liver Metabolism
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批准号:10402862
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项目类别:
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资助金额:$49.5万
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财政年份:2019
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负责人:DAVID J WAXMAN
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依托单位:
Growth Hormone Regulation of Sex Differences in Liver Metabolism
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批准号:10164773
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项目类别:
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资助金额:$49.37万
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财政年份:2019
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负责人:DAVID J WAXMAN
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依托单位:
Growth Hormone Regulation of Sex Differences in Liver Metabolism
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批准号:10018890
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项目类别:
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资助金额:$50.31万
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财政年份:2019
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负责人:DAVID J WAXMAN
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依托单位:
Xenobiotic-responsive hepatic long non-coding RNAs
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批准号:10809269
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项目类别:
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资助金额:$7.78万
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财政年份:2014
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负责人:DAVID J WAXMAN
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依托单位:
Epigenetic Actions of Environmental Chemicals
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批准号:8762618
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项目类别:
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资助金额:$40.39万
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财政年份:2014
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负责人:DAVID J WAXMAN
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依托单位:
Xenobiotic-responsive hepatic long non-coding RNAs
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批准号:10615645
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项目类别:
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资助金额:$47.2万
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财政年份:2014
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负责人:DAVID J WAXMAN
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依托单位:
Xenobiotic-responsive hepatic long non-coding RNAs
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批准号:10394387
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项目类别:
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资助金额:$47.2万
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财政年份:2014
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负责人:DAVID J WAXMAN
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依托单位:
Xenobiotic-responsive hepatic long non-coding RNAs
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批准号:10210396
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项目类别:
-
资助金额:$47.2万
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财政年份:2014
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负责人:DAVID J WAXMAN
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依托单位:
Xenobiotic-responsive hepatic long non-coding RNAs
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批准号:10058507
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项目类别:
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资助金额:$47.2万
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财政年份:2014
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负责人:DAVID J WAXMAN
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依托单位:
Cytochrome P450-Endogenous Substrate Metabolism
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批准号:8037913
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项目类别:
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资助金额:$10.0万
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财政年份:2010
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负责人:DAVID J WAXMAN
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依托单位:
Cytochrome P450-Endogenous Substrate Metabolism
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批准号:7992597
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项目类别:
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资助金额:$9.59万
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财政年份:2009
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负责人:DAVID J WAXMAN
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依托单位:
Epigenetic Marks of Xenoestrogen Exposure
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批准号:8077724
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项目类别:
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资助金额:$8.1万
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财政年份:2009
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负责人:DAVID J WAXMAN
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依托单位:
Epigenetic Marks of Xenoestrogen Exposure
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批准号:7830420
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项目类别:
-
资助金额:$40.1万
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财政年份:2009
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负责人:DAVID J WAXMAN
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依托单位:
Research Project 3: Nuclear Receptors and Gonadal Toxicity of Xenochemicals
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批准号:6901352
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项目类别:
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资助金额:$21.42万
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财政年份:2005
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负责人:DAVID J WAXMAN
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依托单位:
PPAR, hormones, and xenobiotics
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批准号:6664578
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项目类别:
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资助金额:$13.44万
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财政年份:2002
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负责人:DAVID J WAXMAN
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依托单位:
PPAR, hormones, and xenobiotics
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批准号:6578802
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项目类别:
-
资助金额:$13.44万
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财政年份:2002
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负责人:DAVID J WAXMAN
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依托单位:
PPAR, hormones, and xenobiotics
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批准号:6443953
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项目类别:
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资助金额:$13.44万
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财政年份:2001
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负责人:DAVID J WAXMAN
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依托单位:
海外基金