Evidence map›Paper›PMID 26079192›Full record

ReviewEnvironmental science & technology2015

The Aryl Hydrocarbon Receptor: A Key Bridging Molecule of External and Internal Chemical Signals.

Jijing Tian, Yu Feng, Hualing Fu, Heidi Qunhui Xie, Joy Xiaosong Jiang, Bin Zhao

Abstract readReview
In one paragraph

Review in Environmental science & technology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed, 1 pooled it
9.3field-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

46 citing papers in PubMed, 1 synthesis or guideline pooled it, 112 citations in OpenAlex.

  1. Pooled it
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  12. Sustained AhR activity programs memory fate of early effector CD8Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  13. Review
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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

6 authors at 3 institutions in 2 countries.

Jijing Tian†Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Yu Feng†Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Hualing Fu†Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Heidi Qunhui Xie†Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Joy Xiaosong Jiang‡Department of Internal Medicine, Gastroenterology and Hepatology, University of California, Davis, Sacramento, California 95817, United States.
Bin Zhao†Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China.
Chinese Academy of Sciences · CNResearch Center for Eco-Environmental Sciences · CNUniversity of California, Davis · US

Funding

Galectin-3 in Liver FibrosisK01DK090121 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI JIANG, XIAOSONG JOY · 2012 to 2016
$589k
Galectin-3 in Primary biliary CirrhosisR03DK106467 · NIDDK · UNIVERSITY OF CALIFORNIA AT DAVIS · PI JIANG, XIAOSONG JOY · 2015 to 2016
$157k
NIDDK NIH HHS K01 DK090121NIDDK NIH HHS R03 DK106467
6 · The paper itself

Abstract

The aryl hydrocarbon receptor (AhR) is a highly evolutionary conserved, ligand-activated transcription factor that is best known to mediate the toxicities of dioxins and dioxin-like compounds. Phenotype of AhR-null mice, together with the recent discovery of a variety of endogenous and plant-derived ligands, point to the integral roles of AhR in normal cell physiology, in addition to its roles in sensing the environmental chemicals. Here, we summarize the current knowledge about AhR signaling pathways, its ligands and AhR-mediated effects on cell specialization, host defense and detoxification. AhR-mediated health effects particularly in liver, immune, and nervous systems, as well as in tumorgenesis are discussed. Dioxin-initiated embryotoxicity and immunosuppressive effects in fish and birds are reviewed. Recent data demonstrate that AhR is a convergence point of multiple signaling pathways that inform the cell of its external and internal environments. As such, AhR pathway is a promising potential target for therapeutics targeting nervous, liver, and autoimmune diseases through AhR ligand-mediated interventions and other perturbations of AhR signaling. Additionally, using available laboratory data obtained on animal models, AhR-centered adverse outcome pathway analysis is useful in reexamining known and potential adverse outcomes of specific or mixed compounds on wildlife.

Indexed as

Signal TransductionAnimalsDioxinsEvolution, MolecularHealthHumansLigandsReceptors, Aryl HydrocarbonDioxinsLigandsReceptors, Aryl Hydrocarbon

Identifiers

PMID26079192
PMCPMC4696777
OpenAlexW2243372799

What OpenQuestion holds

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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.