Evidence map›Paper›PMID 27568040›Full record

ArticleJournal of molecular medicine (Berlin, Germany)2017

Epidermal growth factor signaling protects from cholestatic liver injury and fibrosis.

Jasmin Svinka, Sandra Pflügler, Markus Mair, Hanns-Ulrich Marschall, Jan G Hengstler, Patricia Stiedl, Valeria Poli, Emilio Casanova, Gerald Timelthaler, Maria Sibilia and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of molecular medicine (Berlin, Germany), 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  6. Article
  7. Review: Pathogenesis of cholestatic liver diseases.World journal of hepatology · 2020
    Review
  8. Article
  9. Review
  10. Article
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

11 authors at 6 institutions in 4 countries.

Jasmin SvinkaInstitute of Cancer Research, Medical University of Vienna & Comprehensive Cancer Center (CCC), Vienna, Austria.
Sandra PflüglerInstitute of Cancer Research, Medical University of Vienna & Comprehensive Cancer Center (CCC), Vienna, Austria.
Markus MairLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Hanns-Ulrich MarschallDepartment of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Jan G HengstlerLeibniz Research Centre for Working Environment and Human Factors at the Technical University of Dortmund (IfADo), Dortmund, Germany.
Patricia StiedlLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Valeria PoliDepartment of Molecular Biotechnology and Health Sciences, Molecular Biotechnology Center, University of Turin, Turin, Italy.
Emilio CasanovaLudwig Boltzmann Institute for Cancer Research (LBI-CR), Vienna, Austria.
Gerald TimelthalerInstitute of Cancer Research, Medical University of Vienna & Comprehensive Cancer Center (CCC), Vienna, Austria.
Maria SibiliaInstitute of Cancer Research, Medical University of Vienna & Comprehensive Cancer Center (CCC), Vienna, Austria.
Robert EferlInstitute of Cancer Research, Medical University of Vienna & Comprehensive Cancer Center (CCC), Vienna, Austria. robert.eferl@meduniwien.ac.at.
Comprehensive Cancer Center Vienna · ATLudwig Boltzmann Institute for Cancer Research · ATMedical University of Vienna · ATTU Dortmund University · DEUniversity of Gothenburg · SEUniversity of Turin · IT

Funding

Austrian Science Fund FWF P 25599Austrian Science Fund FWF P 25925Austrian Science Fund FWF P 26908Austrian Science Fund FWF P 29222
6 · The paper itself

Abstract

We have demonstrated that the signal transducer and activator of transcription 3 (STAT3) protects from cholestatic liver injury. Specific ablation of STAT3 in hepatocytes and cholangiocytes (STAT3 KEY MESSAGE: STAT3 is a negative regulator of bile acid biosynthesis. STAT3 protects from bile acid-induced apoptosis and regulates EGFR expression. EGFR signaling protects from cholestatic liver injury and fibrosis.

Indexed as

AnimalsApoptosisBile Acids and SaltsCaspase 3Caspase 8CholestasisDisease Models, AnimalEpidermal Growth FactorErbB ReceptorsHepatocytesLiver CirrhosisMaleMiceMice, KnockoutMice, TransgenicSignal TransductionBile Acids and SaltsCaspase 3Caspase 8Epidermal Growth FactorErbB ReceptorsSTAT3 Transcription FactorBile acidsCholestasisEpidermal growth factor receptor EGFRHepatocyte apoptosisLiver injurySignal transducer and activator of transcription 3 STAT3

Identifiers

PMID27568040
PMCPMC5225179
OpenAlexW2513000606

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.