Evidence map›Paper›PMID 17463087›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

Cell proliferation and survival induced by Toll-like receptors is antagonized by type I IFNs.

Uzma A Hasan, Christophe Caux, Ivan Perrot, Anne-Claire Doffin, Christine Menetrier-Caux, Giorgio Trinchieri, Massimo Tommasino, Jaromir Vlach

Abstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

33 citing papers in PubMed, 76 citations in OpenAlex.

  1. Article
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  4. CRL4The Journal of experimental medicine · 2018
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  12. Type I IFN-mediated regulation of IL-1 production in inflammatory disorders.Cellular and molecular life sciences : CMLS · 2012
    Review
  13. Toll/interleukin-1 receptor domain-containing adapter inducing interferon-β mediates microglial phagocytosis of degenerating axons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2012
    Article
  14. 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

8 authors at 5 institutions in 2 countries.

Uzma A HasanInfections and Cancer Biology Group, International Agency for Research on Cancer (IARC-WHO), 150 Cours Albert Thomas, 69372 Lyon Cedex 08, France. hasan@iarc.fr
Christophe Caux
Ivan Perrot
Anne-Claire Doffin
Christine Menetrier-Caux
Giorgio Trinchieri
Massimo Tommasino
Jaromir Vlach
Centre Léon Bérard · FRCentre International de Recherche sur le Cancer · FRInnate Pharma (France) · FRNational Cancer Institute · USRockefeller University · US

Funding

Role of inflammation, innate resistance, and immunity in carcinogenesis.ZIABC010793 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TRINCHIERI, GIORGIO · 2009 to 2025
$16.8M
Role of inflammation, innate resistance, and immunity in carcinogenesis.Z01BC010793 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI TRINCHIERI, GIORGIO · 2007 to 2008
$4.2M
6 · The paper itself

Abstract

TRIF is an adaptor protein associated with the signaling by Toll-like receptor (TLR)3 and TLR4 for the induction of type I IFNs. Here, we demonstrate a mechanism by which TLR signaling controls cell proliferation and survival. We show that TLR3 and TLR4 can induce cell cycle entry via TRIF, which targets the cell cycle inhibitor p27(kip1) for relocalization, phosphorylation by cyclin/cdk complexes, and proteasome degradation. These events are antagonized by type I IFN induced by the TRIF pathway. Furthermore, in human dendritic cells treated with TLR3, TLR4, or TLR5 ligands, we demonstrate that IFN signaling modulates p27(kip1) degradation and apoptosis, identifying an immunoregulatory "switching" function of type I IFNs. These findings reveal a previously uncharacterized function of TLR signaling in cell proliferation and survival.

Indexed as

Adaptor Proteins, Vesicular TransportAnimalsApoptosisCell ProliferationCells, CulturedCell SurvivalCyclin-Dependent Kinase Inhibitor p27Dendritic CellsHumansInterferon Type ILipopolysaccharidesNF-kappa BPromoter Regions, GeneticProteasome Endopeptidase ComplexRatsSignal TransductionAdaptor Proteins, Vesicular TransportCyclin-Dependent Kinase Inhibitor p27Interferon Type ILipopolysaccharidesNF-kappa BProteasome Endopeptidase ComplexTICAM1 protein, humanToll-Like Receptor 3Toll-Like Receptor 4

Identifiers

PMID17463087
PMCPMC1876569
OpenAlexW1992752678

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.