Evidence map›Paper›PMID 34047814›Full record

ReviewSeminars in immunopathology2021

The two facets of gp130 signalling in liver tumorigenesis.

Dirk Schmidt-Arras, Eithan Galun, Stefan Rose-John

Open access · hybridAbstract readReview
In one paragraph

Review in Seminars in immunopathology, 2021. 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
0.9field-weighted citation impact, top 23% 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, 12 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Inhibition of gp130 alleviates LPS-induced lung injury by attenuating apoptosis and inflammation through JAK1/STAT3 signaling pathway.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2023
    Article
  9. Mediators of liver inflammation and carcinogenesis.Seminars in immunopathology · 2021
    Article
  10. Endosomes as Signaling Platforms for IL-6 Family Cytokine Receptors.Frontiers in cell and developmental biology · 2021
    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

3 authors at 2 institutions in 2 countries.

Dirk Schmidt-Arras *Institute of Biochemistry, Christian-Albrechts-University Kiel, Kiel, Germany. darras@biochem.uni-kiel.de.ORCID 0000-0002-1072-7495
Eithan Galun *Goldyne Savad Institute of Gene Therapy, Hadassah Medical Centre, Hebrew University Jerusalem, Jerusalem, Israel. EithanG@hadassah.org.il.
Stefan Rose-John *Institute of Biochemistry, Christian-Albrechts-University Kiel, Kiel, Germany. rosejohn@biochem.uni-kiel.de.
Christian-Albrechts-Universität zu Kiel · DEHadassah Medical Center · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The liver is a vital organ with multiple functions and a large regenerative capacity. Tumours of the liver are the second most frequently cause of cancer-related death and develop in chronically inflamed livers. IL-6-type cytokines are mediators of inflammation and almost all members signal via the receptor subunit gp130 and the downstream signalling molecule STAT3. We here summarize current knowledge on how gp130 signalling and STAT3 in tumour cells and cells of the tumour micro-environment drives hepatic tumorigenesis. We furthermore discuss very recent findings describing also anti-tumorigenic roles of gp130/STAT3 and important considerations for therapeutic interventions.

Indexed as

InflammationSignal TransductionCarcinogenesisCytokine Receptor gp130HumansLiverTumor MicroenvironmentCytokine Receptor gp130Anti-tumour immunityCholangiocarcinoma (CCA)gp130Hepatocellular carcinoma (HCC)IL-6InflammationSTAT3Tumour micro-environment

Identifiers

PMID34047814
PMCPMC8443519
OpenAlexW3164431929

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.