Evidence map›Paper›PMID 39261716›Full record

ReviewBritish journal of cancer2024

Specific features of ß-catenin-mutated hepatocellular carcinomas.

Camille Dantzer, Lydia Dif, Justine Vaché, Sara Basbous, Clotilde Billottet, Violaine Moreau

Abstract readReview
In one paragraph

Review in British journal of cancer, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
–field-weighted citation impact
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

29 citing papers in PubMed.

  1. Article
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  7. From Theory to Practice: Which Biomarkers Are Ready for Predicting Response in Advanced HCC?Liver international : official journal of the International Association for the Study of the Liver · 2026
    Review
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  15. Review
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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

6 authors.

Camille DantzerUniversity Bordeaux, INSERM, BRIC, U1312, Bordeaux, France.
Lydia DifUniversity Bordeaux, INSERM, BRIC, U1312, Bordeaux, France.
Justine VachéUniversity Bordeaux, INSERM, BRIC, U1312, Bordeaux, France.
Sara BasbousUniversity Bordeaux, INSERM, BRIC, U1312, Bordeaux, France.
Clotilde Billottet *University Bordeaux, INSERM, BRIC, U1312, Bordeaux, France. clotilde.billottet@u-bordeaux.fr.ORCID http://orcid.org/0000-0003-1819-984X
Violaine Moreau *University Bordeaux, INSERM, BRIC, U1312, Bordeaux, France. violaine.moreau@inserm.fr.ORCID http://orcid.org/0000-0002-4513-7022

Funding

Conseil Régional Aquitaine (Aquitaine Regional Council) PhD fellowshipFondation pour la Recherche Médicale (Foundation for Medical Research in France) DEQ20180839586Ligue Contre le Cancer Comités Gironde et CharentesLigue Contre le Cancer EACMinistère de l'Education Nationale, de l'Enseignement Supérieur et de la Recherche (MENESR) PhD fellowship
6 · The paper itself

Abstract

CTNNB1, encoding the ß-catenin protein, is a key oncogene contributing to liver carcinogenesis. Hepatocellular carcinoma (HCC) is the most common form of primary liver cancer in adult, representing the third leading cause of cancer-related death. Aberrant activation of the Wnt/ß-catenin pathway, mainly due to mutations of the CTNNB1 gene, is observed in a significant subset of HCC. In this review, we first resume the major recent advances in HCC classification with a focus on CTNNB1-mutated HCC subclass. We present the regulatory mechanisms involved in β-catenin stabilisation, transcriptional activity and binding to partner proteins. We then describe specific phenotypic characteristics of CTNNB1-mutated HCC thanks to their unique gene expression patterns. CTNNB1-mutated HCC constitute a full-fledged subclass of HCC with distinct pathological features such as well-differentiated cells with low proliferation rate, association to cholestasis, metabolic alterations, immune exclusion and invasion. Finally, we discuss therapeutic approaches to target ß-catenin-mutated liver tumours and innovative perspectives for future drug developments.

Indexed as

beta CateninCarcinoma, HepatocellularLiver NeoplasmsGene Expression Regulation, NeoplasticHumansMutationWnt Signaling Pathwaybeta CateninCTNNB1 protein, human

Identifiers

PMID39261716
PMCPMC11628615

What OpenQuestion holds

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Registered trials

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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.