2017
DOI: 10.1016/j.tiv.2017.06.025
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Dioxin-like activity of brominated dioxins as individual compounds or mixtures in in vitro reporter gene assays with rat and mouse hepatoma cell lines

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Cited by 14 publications
(4 citation statements)
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“…As shown in Table , the concentration of TCDD-EQ PBDD/DFs was much higher than that of TCDD-EQ PCDD/DFs in DHF effluents. As possible major contributors, PBDD/DFs with dioxin-like activity ,,, were analyzed to evaluate their contribution to the TCDD-EQ PBDD/DFs for the effluents of DHF-3, -4, -8, -9, and -10. The contribution ratio of theoretical TCDD-EQ PBDD/DFs to TCDD-EQ PBDD/DFs ranged from 0.23 to 63% (median: 3.9%) (Tables and S9), indicating that the ratios were very different among the facilities.…”
Section: Discussionmentioning
confidence: 99%
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“…As shown in Table , the concentration of TCDD-EQ PBDD/DFs was much higher than that of TCDD-EQ PCDD/DFs in DHF effluents. As possible major contributors, PBDD/DFs with dioxin-like activity ,,, were analyzed to evaluate their contribution to the TCDD-EQ PBDD/DFs for the effluents of DHF-3, -4, -8, -9, and -10. The contribution ratio of theoretical TCDD-EQ PBDD/DFs to TCDD-EQ PBDD/DFs ranged from 0.23 to 63% (median: 3.9%) (Tables and S9), indicating that the ratios were very different among the facilities.…”
Section: Discussionmentioning
confidence: 99%
“…The concentrations of PBDD/DFs in the extracts were determined by GC–HRMS; the measurement conditions are described in the Supporting Information, and the target compounds and their abbreviations are shown in Table S5. WHO-TEQ or theoretical TCDD-EQ values (WHO-TEQ PBDD/DFs ; theoretical TCDD-EQ PBDD/DFs ) were calculated by multiplying the concentration of each detected PBDD/DF by the WHO-toxicity equivalency factor of their chlorinated analogue or their respective CALUX-REP and then summing the individual WHO-TEQs or theoretical TCDD-EQs to obtain the total WHO-TEQ or theoretical TCDD-EQ.…”
Section: Methodsmentioning
confidence: 99%
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“…Certainly, informative experimental bioassays will be necessary to obtain greater insight on the AhR-ligand interaction modes, and particularly to discriminate between agonistic and antagonistic modulations. One of the most popularized assays is the in vitro AhR Chemically Activated LUciferase eXpression (CALUX) bioassay, which has been reported to be useful in the detection of the AhR antagonistic and agonistic effects of dioxin and dioxin-like chemical compounds [26,27]. This assay is based on the analysis of the induced luciferase response in a recombinant cell line driven by several CYP1A1 dioxin response elements (DREs) as a direct reflection of AhR-mediated transcriptional activity.…”
Section: Introductionmentioning
confidence: 99%