Evidence map›Paper›PMID 31015417›Full record

ArticleNature communications2019

Promotion of growth factor signaling as a critical function of β-catenin during HCC progression.

Eunsun Kim, Amanda Lisby, Connie Ma, Nathanael Lo, Ursula Ehmer, Katharina E Hayer, Emma E Furth, Patrick Viatour

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. 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
6.2field-weighted citation impact, top 3% 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, 98 citations in OpenAlex.

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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

8 authors at 3 institutions in 2 countries.

Eunsun KimChildren's Hospital of Philadelphia, Center for Childhood Cancer Research, Philadelphia, PA, 19104, USA.ORCID http://orcid.org/0000-0001-5909-8768
Amanda LisbyDepartment of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA, 19104, USA.
Connie MaChildren's Hospital of Philadelphia, Center for Childhood Cancer Research, Philadelphia, PA, 19104, USA.
Nathanael LoChildren's Hospital of Philadelphia, Center for Childhood Cancer Research, Philadelphia, PA, 19104, USA.
Ursula EhmerKlinikum rechts der Isar, Technische Universität München, 81675, Munich, Germany.
Katharina E HayerDepartment of Biomedical and Health Informatics, Children's Hospital of Philadelphia, Philadelphia, PA, 19104, USA.ORCID http://orcid.org/0000-0002-1463-3111
Emma E FurthDepartment of Pathology and Laboratory Medicine, Hospital of the University of Pennsylvania, Philadelphia, PA, 19104, USA.
Patrick ViatourChildren's Hospital of Philadelphia, Center for Childhood Cancer Research, Philadelphia, PA, 19104, USA. pviatour@pennmedicine.upenn.edu.
Children's Hospital of Philadelphia · USHospital of the University of Pennsylvania · USTUM Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is the second leading cause of cancer-related deaths worldwide. β-catenin is widely thought to be a major oncogene in HCC based on the frequency of mutations associated with aberrant Wnt signaling in HCC patients. Challenging this model, our data reveal that β-catenin nuclear accumulation is restricted to the late stage of the disease. Until then, β-catenin is primarily located at the plasma membrane in complex with multiple cadherin family members where it drives tumor cell survival by enhancing the signaling of growth factor receptors such as EGFR. Therefore, our study reveals the evolving nature of β-catenin in HCC to establish it as a compound tumor promoter during the progression of the disease.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsAntigens, CDbeta CateninCadherinsCarcinoma, HepatocellularCell Line, TumorCell NucleusDisease ProgressionErbB ReceptorsFemaleHumansLiver CirrhosisLiver NeoplasmsMaleMiceAntigens, CDbeta CateninCadherinsCDH1 protein, humanCDH2 protein, humanCTNNB1 protein, humanEGFR protein, humanErbB ReceptorsWnt3A ProteinWNT3A protein, human

Identifiers

PMID31015417
PMCPMC6478918
OpenAlexW2942354172

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.