Evidence map›Paper›PMID 28508871›Full record

ArticleNature communications2017

Non-cell-autonomous activation of IL-6/STAT3 signaling mediates FGF19-driven hepatocarcinogenesis.

Mei Zhou, Hong Yang, R Marc Learned, Hui Tian, Lei Ling

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

64 citing papers in PubMed, 123 citations in OpenAlex.

  1. Trial
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  8. Cellular Origins and Lineage Plasticity in Cancer.Cold Spring Harbor perspectives in medicine · 2024
    Review
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  11. Alcohol reshapes a liver premetastatic niche for cancer by extra- and intrahepatic crosstalk-mediated immune evasion.Molecular therapy : the journal of the American Society of Gene Therapy · 2023
    Article
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4 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

5 authors at 1 institution in 1 country.

Mei ZhouNGM Biopharmaceuticals, Inc., 333 Oyster Point Boulevard, South San Francisco, California 94080, USA.
Hong YangNGM Biopharmaceuticals, Inc., 333 Oyster Point Boulevard, South San Francisco, California 94080, USA.
R Marc LearnedNGM Biopharmaceuticals, Inc., 333 Oyster Point Boulevard, South San Francisco, California 94080, USA.
Hui TianNGM Biopharmaceuticals, Inc., 333 Oyster Point Boulevard, South San Francisco, California 94080, USA.
Lei LingNGM Biopharmaceuticals, Inc., 333 Oyster Point Boulevard, South San Francisco, California 94080, USA.
NGM Biopharmaceuticals (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC), a primary malignancy of the liver, is the second leading cause of cancer mortality worldwide. Fibroblast Growth Factor 19 (FGF19) is one of the most frequently amplified genes in HCC patients. Moreover, mice expressing an FGF19 transgene have been shown to develop HCC. However, the downstream signalling pathways that mediate FGF19-dependent tumorigenesis remain to be deciphered. Here we show that FGF19 triggers a previously unsuspected, non-cell-autonomous program to activate STAT3 signalling in hepatocytes through IL-6 produced in the liver microenvironment. We show that the hepatocyte-specific deletion of Stat3, genetic ablation of Il6, treatment with a neutralizing anti-IL-6 antibody or administration of a small-molecule JAK inhibitor, abolishes FGF19-induced tumorigenesis, while the regulatory functions of FGF19 in bile acid, glucose and energy metabolism remain intact. Collectively, these data reveal a key role for the IL-6/STAT3 axis in potentiating FGF19-driven HCC in mice, a finding which may have translational relevance in HCC pathogenesis.

Indexed as

Signal TransductionAnimalsBile Acids and SaltsBody CompositionCarcinoma, HepatocellularComputational BiologyDependovirusEnergy MetabolismFemaleFibroblast Growth FactorsGene DeletionGene Expression ProfilingGene Expression Regulation, NeoplasticGlucoseHEK293 CellsHumansBile Acids and SaltsFGF19 protein, humanFibroblast Growth FactorsGlucoseIL6 protein, humanInterleukin-6interleukin-6, mouseSTAT3 protein, humanStat3 protein, mouseSTAT3 Transcription Factor

Identifiers

PMID28508871
PMCPMC5440856
OpenAlexW2616559215

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.