Evidence map›Paper›PMID 22665056›Full record

ArticleOncogene2013

The aryl hydrocarbon receptor regulates focal adhesion sites through a non-genomic FAK/Src pathway.

C Tomkiewicz, L Herry, L-C Bui, C Métayer, M Bourdeloux, R Barouki, X Coumoul

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

52 citing papers in PubMed, 107 citations in OpenAlex.

  1. Review
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  4. Assessment of the relationship between AHR, sdLDL, Klotho biomarkers, and etiologic subtypes in young to middle-aged acute ischemic stroke according to toast classification.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
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  16. AhR and Wnt/β-Catenin Signaling Pathways and Their Interplay.Current issues in molecular biology · 2023
    Review
  17. Review
  18. When AHR signaling pathways meet viral infections.Cell communication and signaling : CCS · 2023
    Review
  19. Article
  20. 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

7 authors at 5 institutions in 1 country.

C TomkiewiczINSERM UMR-S 747, Toxicologie Pharmacologie et Signalisation Cellulaire, Paris, France.
L Herry
L-C Bui
C Métayer
M Bourdeloux
R Barouki
X Coumoul
Université Paris Cité · FRDélégation Paris 5 · FRInserm · FRSorbonne Paris Cité · FRToxicologie, Pharmacologie et Signalisation Cellulaire · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aryl hydrocarbon receptor (AhR) is commonly described as a transcription factor, which regulates xenobiotic-metabolizing enzymes. Recent studies have suggested that the binding of ligands to the AhR also activates the Src kinase. In this manuscript, we show that the AhR, through the activation of Src, activates focal adhesion kinase (FAK) and promotes integrin clustering. These effects contribute to cell migration. Further, we show that the activation of the AhR increases the interaction of FAK with the metastatic marker, HEF1/NEDD9/CAS-L, and the expression of several integrins. Xenobiotic exposure, thus, may contribute to novel cell-migratory programs.

Indexed as

Adaptor Proteins, Signal TransducingApoptosisBlotting, WesternCell AdhesionCell MovementCell ProliferationFluorescent Antibody TechniqueFocal Adhesion Protein-Tyrosine KinasesFocal AdhesionsHep G2 CellsHumansImmunoenzyme TechniquesImmunoprecipitationIntegrin beta1PhosphoproteinsPhosphorylationAdaptor Proteins, Signal TransducingFocal Adhesion Protein-Tyrosine KinasesIntegrin beta1NEDD9 protein, humanPhosphoproteinsReceptors, Aryl HydrocarbonRNA, Messengersrc-Family Kinases

Identifiers

PMID22665056
OpenAlexW1973330653

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.