Cargando…

Differences in TCDD-elicited gene expression profiles in human HepG2, mouse Hepa1c1c7 and rat H4IIE hepatoma cells

BACKGROUND: 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is an environmental contaminant that elicits a broad spectrum of toxic effects in a species-specific manner. Current risk assessment practices routinely extrapolate results from in vivo and in vitro rodent models to assess human risk. In order t...

Descripción completa

Detalles Bibliográficos
Autores principales: Dere, Edward, Lee, Andrea W, Burgoon, Lyle D, Zacharewski, Timothy R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089798/
https://www.ncbi.nlm.nih.gov/pubmed/21496263
http://dx.doi.org/10.1186/1471-2164-12-193
_version_ 1782203081178480640
author Dere, Edward
Lee, Andrea W
Burgoon, Lyle D
Zacharewski, Timothy R
author_facet Dere, Edward
Lee, Andrea W
Burgoon, Lyle D
Zacharewski, Timothy R
author_sort Dere, Edward
collection PubMed
description BACKGROUND: 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is an environmental contaminant that elicits a broad spectrum of toxic effects in a species-specific manner. Current risk assessment practices routinely extrapolate results from in vivo and in vitro rodent models to assess human risk. In order to further investigate the species-specific responses elicited by TCDD, temporal gene expression responses in human HepG2, mouse Hepa1c1c7 and rat H4IIE cells were compared. RESULTS: Microarray analysis identified a core set of conserved gene expression responses across species consistent with the role of AhR in mediating adaptive metabolic responses. However, significant species-specific as well as species-divergent responses were identified. Computational analysis of the regulatory regions of species-specific and -divergent responses suggests that dioxin response elements (DREs) are involved. These results are consistent with in vivo rat vs. mouse species-specific differential gene expression, and more comprehensive comparative DRE searches. CONCLUSIONS: Comparative analysis of human HepG2, mouse Hepa1c1c7 and rat H4IIE TCDD-elicited gene expression responses is consistent with in vivo rat-mouse comparative gene expression studies, and more comprehensive comparative DRE searches, suggesting that AhR-mediated gene expression is species-specific.
format Text
id pubmed-3089798
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-30897982011-05-08 Differences in TCDD-elicited gene expression profiles in human HepG2, mouse Hepa1c1c7 and rat H4IIE hepatoma cells Dere, Edward Lee, Andrea W Burgoon, Lyle D Zacharewski, Timothy R BMC Genomics Research Article BACKGROUND: 2,3,7,8-Tetrachlorodibenzo-p-dioxin (TCDD) is an environmental contaminant that elicits a broad spectrum of toxic effects in a species-specific manner. Current risk assessment practices routinely extrapolate results from in vivo and in vitro rodent models to assess human risk. In order to further investigate the species-specific responses elicited by TCDD, temporal gene expression responses in human HepG2, mouse Hepa1c1c7 and rat H4IIE cells were compared. RESULTS: Microarray analysis identified a core set of conserved gene expression responses across species consistent with the role of AhR in mediating adaptive metabolic responses. However, significant species-specific as well as species-divergent responses were identified. Computational analysis of the regulatory regions of species-specific and -divergent responses suggests that dioxin response elements (DREs) are involved. These results are consistent with in vivo rat vs. mouse species-specific differential gene expression, and more comprehensive comparative DRE searches. CONCLUSIONS: Comparative analysis of human HepG2, mouse Hepa1c1c7 and rat H4IIE TCDD-elicited gene expression responses is consistent with in vivo rat-mouse comparative gene expression studies, and more comprehensive comparative DRE searches, suggesting that AhR-mediated gene expression is species-specific. BioMed Central 2011-04-15 /pmc/articles/PMC3089798/ /pubmed/21496263 http://dx.doi.org/10.1186/1471-2164-12-193 Text en Copyright ©2011 Dere et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dere, Edward
Lee, Andrea W
Burgoon, Lyle D
Zacharewski, Timothy R
Differences in TCDD-elicited gene expression profiles in human HepG2, mouse Hepa1c1c7 and rat H4IIE hepatoma cells
title Differences in TCDD-elicited gene expression profiles in human HepG2, mouse Hepa1c1c7 and rat H4IIE hepatoma cells
title_full Differences in TCDD-elicited gene expression profiles in human HepG2, mouse Hepa1c1c7 and rat H4IIE hepatoma cells
title_fullStr Differences in TCDD-elicited gene expression profiles in human HepG2, mouse Hepa1c1c7 and rat H4IIE hepatoma cells
title_full_unstemmed Differences in TCDD-elicited gene expression profiles in human HepG2, mouse Hepa1c1c7 and rat H4IIE hepatoma cells
title_short Differences in TCDD-elicited gene expression profiles in human HepG2, mouse Hepa1c1c7 and rat H4IIE hepatoma cells
title_sort differences in tcdd-elicited gene expression profiles in human hepg2, mouse hepa1c1c7 and rat h4iie hepatoma cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3089798/
https://www.ncbi.nlm.nih.gov/pubmed/21496263
http://dx.doi.org/10.1186/1471-2164-12-193
work_keys_str_mv AT dereedward differencesintcddelicitedgeneexpressionprofilesinhumanhepg2mousehepa1c1c7andrath4iiehepatomacells
AT leeandreaw differencesintcddelicitedgeneexpressionprofilesinhumanhepg2mousehepa1c1c7andrath4iiehepatomacells
AT burgoonlyled differencesintcddelicitedgeneexpressionprofilesinhumanhepg2mousehepa1c1c7andrath4iiehepatomacells
AT zacharewskitimothyr differencesintcddelicitedgeneexpressionprofilesinhumanhepg2mousehepa1c1c7andrath4iiehepatomacells