| Literature DB >> 31453421 |
Stephen Safe1, Huajun Han2,3,4, Jennifer Goldsby3,4, Kumaravel Mohankumar1, Robert S Chapkin2,3,4.
Abstract
The aryl hydrocarbon receptor (AhR) binds structurally diverse ligands that vary from the environmental toxicant 2,3,7,8-tetrachlorodibenzo-B-dioxin (TCDD) to AhR- active pharmaceuticals and health-promoting phytochemicals. There are remarkable differences in the toxicity of TCDD and related halogenated aromatics (HAs) vs. health promoting AhR ligands, and genomic analysis shows that even among the toxic HAs, there are differences in their regulation of genes and pathways. Thus, like ligands for other receptors, AhR ligands are selective AhR modulators (SAhRMs) which exhibit variable tissue-, organ- and species-specific genomic and functional activities.Entities:
Keywords: AhR; ligands; structure-activity genomic differences
Year: 2018 PMID: 31453421 PMCID: PMC6709982 DOI: 10.1016/j.cotox.2018.11.005
Source DB: PubMed Journal: Curr Opin Toxicol ISSN: 2468-2020