Evidence map›Paper›PMID 8164674›Full record

ArticleMolecular and cellular biology1994

The interleukin-6-activated acute-phase response factor is antigenically and functionally related to members of the signal transducer and activator of transcription (STAT) family.

U M Wegenka, C Lütticken, J Buschmann, J Yuan, F Lottspeich, W Müller-Esterl, C Schindler, E Roeb, P C Heinrich, F Horn

Open access · greenAbstract readComparative Study
In one paragraph

Article in Molecular and cellular biology, 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
13.6field-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

67 citing papers in PubMed, 252 citations in OpenAlex.

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  20. RTK signaling requires C3ar1/C5ar1 and IL-6R joint signaling to repress dominant PTEN, SOCS1/3 and PHLPP restraint.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article

7 more citing papers are in PubMed but not listed here.

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

10 authors at 1 institution in 1 country.

U M WegenkaInstitute of Biochemistry, RWTH Aachen, Germany.
C Lütticken
J Buschmann
J Yuan
F Lottspeich
W Müller-Esterl
C Schindler
E Roeb
P C Heinrich
F Horn
RWTH Aachen University · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-6 (IL-6), leukemia inhibitory factor, oncostatin M, IL-11, and ciliary neurotropic factor are a family of cytokines and neuronal differentiation factors which bind to composite plasma membrane receptors sharing the signal transducing subunit gp130. We have shown recently that IL-6 and leukemia inhibitory factor rapidly activate a latent cytoplasmic transcription factor, acute-phase response factor (APRF), by tyrosine phosphorylation, which then binds to IL-6 response elements of various IL-6 target genes. Here we demonstrate that APRF is activated by all cytokines acting through gp130 and is detected in a wide variety of cell types, indicating a central role of this transcription factor in gp130-mediated signaling. APRF activation is also observed in vitro upon addition of IL-6 to cell homogenates. Protein tyrosine kinase inhibitors block both the tyrosine phosphorylation and DNA binding of APRF. The factor was purified to homogeneity from rat liver and shown to consist of a single 87-kDa polypeptide, while two forms (89 and 87 kDa) are isolated from human hepatoma cells. As reported earlier, the binding sequence specificity of APRF is shared by gamma interferon (IFN-gamma) activation factor, which is formed by the Stat91 protein. Partial amino acid sequence obtained from purified rat APRF demonstrated that it is likely to be related to Stat91. In fact, an antiserum raised against the amino-terminal portion of Stat91 cross-reacted with APRF, suggesting the relatedness of APRF and Stat91. Altogether, these data indicate that APRF belongs to a growing family of Stat-related proteins and that IFN-gamma and IL-6 use similar signaling pathways to activate IFN-gamma activation factor and APRF, respectively.

Indexed as

Trans-ActivatorsTyrphostins3T3 CellsAlkaloidsAmino Acid SequenceAnimalsBase SequenceCarcinoma, HepatocellularCatecholsCell LineCytokinesDNA-Binding ProteinsGenisteinGrowth InhibitorsHumansImmune SeraAlkaloidsCatecholsCytokinesDNA-Binding ProteinsGenisteinGrowth InhibitorsImmune SeraInterferon-gammaInterleukin-11Interleukin-6IsoflavonesLeukemia Inhibitory FactorLIF protein, humanLif protein, mouseLymphokinesNerve Growth FactorsNerve Tissue ProteinsNitrilesOligodeoxyribonucleotidesOncostatin MOSM protein, humanOsm protein, mousePeptidesProtein Kinase InhibitorsRecombinant ProteinsSphingosineSTAT3 protein, humanStat3 protein, mouseStat3 protein, ratSTAT3 Transcription FactorStaurosporineTrans-ActivatorsTranscription Factorstyrphostin 47Tyrphostins

Identifiers

PMID8164674
PMCPMC358686
OpenAlexW1822742523

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.