Evidence map›Paper›PMID 15598615›Full record

ArticleEnvironmental health perspectives2004

Subchronic exposure to TCDD, PeCDF, PCB126, and PCB153: effect on hepatic gene expression.

Chad M Vezina, Nigel J Walker, James R Olson

Open access · diamondAbstract read
In one paragraph

Article in Environmental health perspectives, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
8.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 166 citations in OpenAlex.

  1. Article
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  9. Review
  10. Article
  11. Article
  12. Review
  13. Dietary Manganese Modulates PCB126 Toxicity, Metal Status, and MnSOD in the Rat.Toxicological sciences : an official journal of the Society of Toxicology · 2016
    Article
  14. Article
  15. Article
  16. Article
  17. Intersection of AHR and Wnt signaling in development, health, and disease.International journal of molecular sciences · 2014
    Review
  18. Article
  19. Article
  20. Toxicogenomic evaluation of long-term hepatic effects of TCDD in immature, ovariectomized C57BL/6 mice.Toxicological sciences : an official journal of the Society of Toxicology · 2013
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors at 3 institutions in 1 country.

Chad M VezinaUniversity of Wisconsin-Madison, School of Pharmacy, Madison, Wisconsin, USA.
Nigel J Walker
James R Olson
National Institute of Environmental Health Sciences · USUniversity at Buffalo, State University of New York · USUniversity of Wisconsin–Madison · US

Funding

INDUCTION OF CYP450S BY DIOXINSR03ES009440 · NIEHS · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI OLSON, JAMES R · 1998 to 1998
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Statistical Methods And Applications For Laboratory AnimZ01ES046004 · NIEHS · ENVIRONMENTAL HEALTH SCIENCES · PI WALKER, NIGEL J · 1985 to 2006
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NIEHS NIH HHS ES 09440
6 · The paper itself

Abstract

We employed DNA microarray to identify unique hepatic gene expression patterns associated with subchronic exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and other halogenated aromatic hydrocarbons (HAHs). Female Harlan Sprague-Dawley rats were exposed for 13 weeks to toxicologically equivalent doses of four different HAHs based on the toxic equivalency factor of each chemical: TCDD (100 ng/kg/day), 2,3,4,7,8-pentachlorodibenzofuran (PeCDF; 200 ng/kg/day), 3,3',4,4',5-pentachlorobiphenyl (PCB126; 1,000 ng/kg/day), or 2,2',4,4',5,5'-hexachlorobiphenyl (PCB153; 1,000 microg/kg/day). Global gene expression profiles for each exposure, which account for 8,799 gene probe sets contained on Affymetrix RGU34A GeneChips, were compared by principal components analysis. The aryl hydrocarbon receptor (AhR) ligands TCDD, PeCDF, and PCB126 produced very similar global gene expression profiles that were unique from the nonAhR ligand PCB153, underscoring the extensive impact of AhR activation and/or the resulting hepatic injury on global gene expression in female rat liver. Many genes were co-expressed during the 13-week TCDD, PeCDF, or PCB126 exposures, including classical AhR-regulated genes and some genes not previously characterized as being AhR regulated, such as carcinoembryonic-cell adhesion molecule 4 (C-CAM4) and adenylate cyclase-associated protein 2 (CAP2). Real-time reverse-transcriptase polymerase chain reaction confirmed the increased expression of these genes in TCDD-, PeCDF-, and PCB126-exposed rats as well as the up- or down-regulation of several other novel dioxin-responsive genes. In summary, DNA microarray successfully identified dioxin-responsive genes expressed after exposure to AhR ligands (TCDD, PeCDF, PCB126) but not after exposure to the non-AhR ligand PCB153. Together, these findings may help to elucidate some of the fundamental features of dioxin toxicity and may further clarify the biologic role of the AhR signaling pathway.

Indexed as

Gene Expression ProfilingAdministration, OralAnimalsBenzofuransDNA PrimersFemaleGene Expression RegulationHydrocarbons, HalogenatedLiverPolychlorinated BiphenylsPolychlorinated DibenzodioxinsRatsRats, Sprague-DawleyReverse Transcriptase Polymerase Chain ReactionRNA2,3,4,7,8-pentachlorodibenzofuran2,4,5,2',4',5'-hexachlorobiphenyl3,4,5,3',4'-pentachlorobiphenylBenzofuransDNA PrimersHydrocarbons, HalogenatedPolychlorinated BiphenylsPolychlorinated DibenzodioxinsRNA

Identifiers

PMID15598615
PMCPMC1247661
OpenAlexW1967179667

What OpenQuestion holds

Textmetadata
LicenceCC0
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.