Antioxidant functions of the aryl hydrocarbon receptor (AhR)

dc.contributor.authorDietrich, Cornelia
dc.date.accessioned2022-06-20T07:47:04Z
dc.date.available2022-06-20T07:47:04Z
dc.date.issued2016
dc.description.abstractThe aryl hydrocarbon receptor (AhR) is a transcription factor belonging to the basic helix-loop-helix/PER-ARNT-SIM family. It is activated by a variety of ligands, such as environmental contaminants like polycyclic aromatic hydrocarbons or dioxins, but also by naturally occurring compounds and endogenous ligands. Binding of the ligand leads to dimerization of the AhR with aryl hydrocarbon receptor nuclear translocator (ARNT) and transcriptional activation of several xenobiotic phase I and phase II metabolizing enzymes. It is generally accepted that the toxic responses of polycyclic aromatic hydrocarbons, dioxins, and structurally related compounds are mediated by activation of the AhR. A multitude of studies indicate that the AhR operates beyond xenobiotic metabolism and exerts pleiotropic functions. Increasing evidence points to a protective role of the AhR against carcinogenesis and oxidative stress. Herein, I will highlight data demonstrating a causal role of the AhR in the antioxidant response and present novel findings on potential AhR-mediated antioxidative mechanisms.en_GB
dc.description.sponsorshipDFG, Open Access-Publizieren Universität Mainz / Universitätsmedizinde
dc.identifier.doihttp://doi.org/10.25358/openscience-7166
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/7180
dc.language.isoengde
dc.rightsCC-BY-4.0*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleAntioxidant functions of the aryl hydrocarbon receptor (AhR)en_GB
dc.typeZeitschriftenaufsatzde
jgu.journal.titleStem cells internationalde
jgu.journal.volume2016de
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number2700
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternativeArt. 7943495de
jgu.publisher.doi10.1155/2016/7943495de
jgu.publisher.issn1687-9678de
jgu.publisher.nameSage-Hindawide
jgu.publisher.placeLondon u.a.de
jgu.publisher.urihttp://dx.doi.org/10.1155/2016/7943495de
jgu.publisher.year2016
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode610de
jgu.type.dinitypeArticleen_GB
jgu.type.resourceTextde
jgu.type.versionPublished versionde
opus.affiliatedDietrich, Cornelia
opus.date.modified2018-08-23T08:53:51Z
opus.identifier.opusid56423
opus.institute.number0414
opus.metadataonlyfalse
opus.organisation.stringFB 04: Medizin: Institut für Toxikologiede_DE
opus.subject.dfgcode00-000
opus.type.contenttypeKeinede_DE
opus.type.contenttypeNoneen_EN

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