Evidence map›Paper›PMID 24812009›Full record

ArticleToxicological sciences : an official journal of the Society of Toxicology2014

Human receptor activation by aroclor 1260, a polychlorinated biphenyl mixture.

Banrida Wahlang, K Cameron Falkner, Heather B Clair, Laila Al-Eryani, Russell A Prough, J Christopher States, Denise M Coslo, Curtis J Omiecinski, Matthew C Cave

Open access · bronzeAbstract readValidation Study
In one paragraph

Article in Toxicological sciences : an official journal of the Society of Toxicology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
10.6field-weighted citation impact, top 2% 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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 102 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Epidermal growth factor receptor in placental health and disease: pathways, dysfunction, and chemical disruption.Toxicological sciences : an official journal of the Society of Toxicology · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Hydroxylation markedly alters how the polychlorinated biphenyl (PCB) congener, PCB52, affects gene expression in human preadipocytes.Toxicology in vitro : an international journal published in association with BIBRA · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Pregnane X Receptor and the Gut-Liver Axis: A Recent Update.Drug metabolism and disposition: the biological fate of chemicals · 2022
    Review
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

9 authors at 3 institutions in 1 country.

Banrida WahlangDepartment of Pharmacology and Toxicology.
K Cameron FalknerDepartment of Medicine, Division of Gastroenterology, Hepatology and Nutrition.
Heather B ClairDepartment of Biochemistry and Molecular Biology, University of Louisville School of Medicine, Louisville, Kentucky 40202.
Laila Al-EryaniDepartment of Pharmacology and Toxicology.
Russell A ProughDepartment of Biochemistry and Molecular Biology, University of Louisville School of Medicine, Louisville, Kentucky 40202.
J Christopher StatesDepartment of Pharmacology and Toxicology.
Denise M CosloCenter for Molecular Toxicology, Penn State University, University Park, Pennsylvania 16802.
Curtis J OmiecinskiCenter for Molecular Toxicology, Penn State University, University Park, Pennsylvania 16802.
Matthew C CaveDepartment of Pharmacology and Toxicology Department of Medicine, Division of Gastroenterology, Hepatology and Nutrition The Robley Rex Veterans Affairs Medical Center, Louisville, Kentucky 40206 matt.cave@louisville.edu.
Pennsylvania State University · USUniversity of Louisville · USLouisville VA Medical Center · US

Funding

Targeting Dynamics of CAR and PXR in the Mouse and Human GenomesR01GM066411 · NIGMS · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI OMIECINSKI, CURTIS J · 2002 to 2017
$4.5M
PCBs worsen obesity/metabolic syndrome through 'toxic metabolic endotoxemia'R01ES021375 · NIEHS · UNIVERSITY OF LOUISVILLE · PI CAVE, MATTHEW C · 2012 to 2016
$1.7M
Zinc supplementation in alcoholic cirrhosisK23AA018399 · NIAAA · UNIVERSITY OF LOUISVILLE · PI CAVE, MATTHEW C · 2010 to 2014
$1.0M
Summer Environmental Health Sciences Training ProgramT35ES014559 · NIEHS · UNIVERSITY OF LOUISVILLE · PI Matthew C Cave, Daniel Joseph Conklin · 2006 to 2026
$751k
NIAAA NIH HHS K23AA018399NIEHS NIH HHS 1R01ES021375NIEHS NIH HHS R01 ES021375NIEHS NIH HHS T35ES14559NIGMS NIH HHS 5R01GM066411
6 · The paper itself

Abstract

Polychlorinated biphenyls (PCBs) are persistent environmental toxicants, present in 100% of U.S. adults and dose-dependently associated with obesity and non-alcoholic fatty liver disease (NAFLD). PCBs are predicted to interact with receptors previously implicated in xenobiotic/energy metabolism and NAFLD. These receptors include the aryl hydrocarbon receptor (AhR), pregnane xenobiotic receptor (PXR), constitutive androstane receptor (CAR), peroxisome proliferator-activated receptors (PPARs), liver-X-receptor (LXRα), and farnesoid-X-receptor (FXR). This study evaluates Aroclor 1260, a PCB mixture with congener composition mimicking that of human adipose tissue, and selected congeners, as potential ligands for these receptors utilizing human hepatoma-derived (HepG2) and primate-derived (COS-1) cell lines, and primary human hepatocytes. Aroclor 1260 (20 μg/ml) activated AhR, and PCB 126, a minor component, was a potent inducer. Aroclor 1260 activated PXR in a simple concentration-dependent manner at concentrations ≥10 μg/ml. Among the congeners tested, PCBs 138, 149, 151, 174, 183, 187, and 196 activated PXR. Aroclor 1260 activated CAR2 and CAR3 variants at lower concentrations and antagonize CAR2 activation by the CAR agonist, CITCO, at higher concentrations (≥20 μg/ml). Additionally, Aroclor 1260 induced CYP2B6 in primary hepatocytes. At subtoxic doses, Aroclor 1260 did not activate LXR or FXR and had no effect on LXR- or FXR-dependent induction by the agonists T0901317 or GW4064, respectively. Aroclor 1260 (20 μg/ml) suppressed PPARα activation by the agonist nafenopin, although none of the congeners tested demonstrated significant inhibition. The results suggest that Aroclor 1260 is a human AhR, PXR and CAR3 agonist, a mixed agonist/antagonist for CAR2, and an antagonist for human PPARα.

Indexed as

AroclorsBase SequenceComplex MixturesDNA PrimersHep G2 CellsHumansaroclor 1260AroclorsComplex MixturesDNA PrimersAroclor 1260aryl hydrocarbon receptornuclear receptorsPCBs

Identifiers

PMID24812009
PMCPMC4176050
OpenAlexW2104564665

What OpenQuestion holds

Textmetadata
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.