Evidence map›Paper›PMID 19768137›Full record

ArticleEnvironmental toxicology and pharmacology2008

Receptor interactions by polybrominated diphenyl ethers versus polychlorinated biphenyls: a theoretical Structure-activity assessment.

G Luthe, J A Jacobus, L W Robertson

Open access · greenAbstract read
In one paragraph

Article in Environmental toxicology and pharmacology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.4field-weighted citation impact, top 22% 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

22 citing papers in PubMed, 79 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Identifying sex differences arising from polychlorinated biphenyl exposures in toxicant-associated liver disease.Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association · 2019
    Article
  8. Article
  9. Article
  10. Article
  11. Editor's Highlight: PCB126 Exposure Increases Risk for Peripheral Vascular Diseases in a Liver Injury Mouse Model.Toxicological sciences : an official journal of the Society of Toxicology · 2017
    Article
  12. Article
  13. Polychlorinated biphenyl exposure alters the expression profile of microRNAs associated with vascular diseases.Toxicology in vitro : an international journal published in association with BIBRA · 2016
    Article
  14. PCDDs, PCDFs, and PCBs co-occurrence in TiO2 nanoparticles.Environmental science and pollution research international · 2016
    Article
  15. Article
  16. Article
  17. Article
  18. Metabolism and metabolites of polychlorinated biphenyls.Critical reviews in toxicology · 2015
    Review
  19. Human receptor activation by aroclor 1260, a polychlorinated biphenyl mixture.Toxicological sciences : an official journal of the Society of Toxicology · 2014
    Article
  20. 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 1 institution in 1 country.

G LutheDepartment of Occupational and Environmental Health, University of Iowa, 100 Oakdale Campus # 124 IREH, Iowa City, IA 52242-5000, USA.
J A Jacobus
L W Robertson
University of Iowa · US

Funding

Training CoreP42ES013661 · NIEHS · UNIVERSITY OF IOWA · PI Keri C Hornbuckle · 2006 to 2026
$60.3M
Pulmonary Toxicology Facility CoreP30ES005605 · NIEHS · UNIVERSITY OF IOWA · PI HANS-JOACHIM LEHMLER · 1990 to 2026
$40.5M
NIEHS NIH HHS P30 ES005605NIEHS NIH HHS P42 ES013661
6 · The paper itself

Abstract

The extensive body of literature regarding the interaction of polychlorinated biphenyls (PCBs) with transcription factors (receptors) has great value to understand similarities and distinctions and in formulating hypotheses regarding the activity of polybrominated diphenyl ethers (PBDEs) toward those same receptors. Our goal is to present the most comprehensive overview of PBDE effects on AhR, CAR, PXR, ER, AR, PR, DHT, TH, T3, T4 and IGF, as well as hypothetical biological activities of PPAR, RyR, GR and GABA. Aside the influence of the conformation of the ligand, we discuss its constitution influencing the binding affinity: size and polarizability, hydrophilicity, Gibbs free energy of solvation, inductive and mesomeric effects. We evaluate the techniques to determine the biologically relevant conformation of these halogenated hydrocarbons, including computation methods, X-ray and microwave spectroscopy. A novel fluoro-tagged ligand approach holds promise as tools for illuminating the steric and electronic effects in ligand-receptor interaction. Based on our assessment, we predict that PBDEs do not exhibit AhR activity themselves, but impurities are responsible for these effects.

Indexed as

AhRARBinding affinityCARConformationConstitutionDHTERGABAGibbs free solvation energyGRHydrophilicityIGFInductive effectsMesomeric effectsPBDEsPCBsPolarizabilitypolybrominated diphenyl etherspolychlorinated biphenylsPPARPRPXRRyRT3T4TH

Identifiers

PMID19768137
PMCPMC2746664
OpenAlexW1975036542

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.