Evidence map›Paper›PMID 19027718›Full record

ReviewBiochemical pharmacology2009

Timing is everything: consequences of transient and sustained AhR activity.

Kristen A Mitchell, Cornelis J Elferink

Open access · greenAbstract readComparative StudyReview
In one paragraph

Review in Biochemical pharmacology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 48 papers.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

48 citing papers in PubMed, 120 citations in OpenAlex.

  1. Review
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  13. Observational
  14. Review
  15. The aryl hydrocarbon receptor facilitates the human cytomegalovirus-mediated G1/S block to cell cycle progression.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  16. Review
  17. Review
  18. Article
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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

2 authors at 1 institution in 1 country.

Kristen A MitchellDepartment of Pharmacology and Toxicology, and Sealy Center for Cancer Cell Biology, School of Medicine, University of Texas Medical Branch, 301 University Boulevard, Galveston, TX 77555-1031, USA.
Cornelis J Elferink
The University of Texas Medical Branch at Galveston · US

Funding

Synthetic Organic Chemistry CoreP30ES006676 · NIEHS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI ELFERINK, CORNELIS JOHAN · 1995 to 2017
$21.7M
Ah Receptor Anatomy: Implications for Dioxin ToxicityR01ES007800 · NIEHS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI ELFERINK, CORNELIS JOHAN · 2001 to 2011
$3.5M
Ah Receptor Action and ApoptosisR01ES012018 · NIEHS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI ELFERINK, CORNELIS JOHAN · 2005 to 2010
$1.8M
Role of cytochrome P4501A1 in cell cycle progressionF32ES013588 · NIEHS · UNIVERSITY OF TEXAS MEDICAL BR GALVESTON · PI MITCHELL, KRISTEN ANDREA · 2004 to 2005
$91k
NIEHS NIH HHS F32 ES013588NIEHS NIH HHS F32ES013588NIEHS NIH HHS P30 ES006676NIEHS NIH HHS R01 ES007800NIEHS NIH HHS R01ES007800NIEHS NIH HHS R01 ES012018NIEHS NIH HHS R01ES012018
6 · The paper itself

Abstract

The aryl hydrocarbon receptor (AhR) was implicated as a mediator of xenobiotic toxicity over three decades ago. Although a complete picture continues to elude us, investigations by many laboratories during the ensuing period have revealed much about AhR biology in normal physiological processes, as well as the toxicities induced by the dioxins and related polychlorinated aromatic hydrocarbons. The findings are captured in numerous excellent reviews. This commentary attempts to inject a new perspective on some new as well as frequently overlooked observations in the context of established receptor properties. Specifically, we examine the impact of transient versus sustained receptor activation on AhR biology, and explore the potential role for cytochrome P450 expression in regulating AhR activity amongst various tissues. The growing recognition that AhR action functions through multiple mechanisms serves to further highlight the importance of limiting prolonged receptor activation.

Indexed as

AnimalsAryl Hydrocarbon HydroxylasesHumansOrgan SpecificityReceptors, Aryl HydrocarbonTime FactorsXenobioticsAryl Hydrocarbon HydroxylasesReceptors, Aryl HydrocarbonXenobiotics

Identifiers

PMID19027718
PMCPMC2751579
OpenAlexW1997382475

What OpenQuestion holds

Textmetadata
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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.