Evidence map›Paper›PMID 25021421›Full record

ArticleGut2015

Integration of tumour and viral genomic characterizations in HBV-related hepatocellular carcinomas.

Giuliana Amaddeo, Qian Cao, Yannick Ladeiro, Sandrine Imbeaud, Jean-Charles Nault, Daphne Jaoui, Yann Gaston Mathe, Christophe Laurent, Alexis Laurent, Paulette Bioulac-Sage and 2 more

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Gut, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed, 1 pooled it
10.9field-weighted citation impact, top 1% 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

91 citing papers in PubMed, 1 synthesis or guideline pooled it, 158 citations in OpenAlex.

  1. Pooled it
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  7. Article
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  12. mRNA-Based Engineering of Viral Antigen-Specific TCR-T Cells.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
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  16. Article
  17. Tumor Antigens beyond the Human Exome.International journal of molecular sciences · 2024
    Review
  18. Article
  19. Article
  20. Review

31 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors at 3 institutions in 1 country.

Giuliana AmaddeoInserm, UMR-674, Génomique fonctionnelle des tumeurs solides, IUH, Paris, France Université Paris Descartes, Labex Immuno-oncology, Sorbonne Paris Cité, Faculté de Médecine, Paris, France.
Qian CaoInserm, UMR-674, Génomique fonctionnelle des tumeurs solides, IUH, Paris, France Université Paris Descartes, Labex Immuno-oncology, Sorbonne Paris Cité, Faculté de Médecine, Paris, France.
Yannick LadeiroInserm, UMR-674, Génomique fonctionnelle des tumeurs solides, IUH, Paris, France Université Paris Descartes, Labex Immuno-oncology, Sorbonne Paris Cité, Faculté de Médecine, Paris, France.
Sandrine ImbeaudInserm, UMR-674, Génomique fonctionnelle des tumeurs solides, IUH, Paris, France Université Paris Descartes, Labex Immuno-oncology, Sorbonne Paris Cité, Faculté de Médecine, Paris, France.
Jean-Charles NaultInserm, UMR-674, Génomique fonctionnelle des tumeurs solides, IUH, Paris, France Université Paris Descartes, Labex Immuno-oncology, Sorbonne Paris Cité, Faculté de Médecine, Paris, France.
Daphne JaouiHypercube research, France.
Yann Gaston MatheHypercube research, France.
Christophe LaurentDepartment of Surgery, CHU de Bordeaux, Bordeaux, France.
Alexis LaurentAssistance Publique-Hôpitaux de Paris, digestive, hepatobiliary and liver transplantation, CHU Henri Mondor, Créteil, France IMRB-Inserm U955 Equipe n. 18 "Virologie moleculaire et immunologie -Physiopathologie et therapeutique des Hépatites virales chroniques", Créteil, France.
Paulette Bioulac-SageInserm, UMR-1053; Université Victor Segalen Bordeaux 2, Bordeaux, France Department of Pathology, CHU de Bordeaux, Pellegrin Hospital, Bordeaux, France.
Julien CalderaroInserm, UMR-674, Génomique fonctionnelle des tumeurs solides, IUH, Paris, France Université Paris Descartes, Labex Immuno-oncology, Sorbonne Paris Cité, Faculté de Médecine, Paris, France Department of Pathology, CHU Henri Mondor, Créteil, France.
Jessica Zucman-RossiInserm, UMR-674, Génomique fonctionnelle des tumeurs solides, IUH, Paris, France Université Paris Descartes, Labex Immuno-oncology, Sorbonne Paris Cité, Faculté de Médecine, Paris, France Hopital Europeen Georges Pompidou, Paris, France.ORCID http://orcid.org/0000-0002-5687-0334
Délégation Paris 5 · FRInserm · FRCentre Hospitalier Universitaire de Bordeaux · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimHepatocellular carcinoma (HCC) is the most common liver cancer. We characterised HCC associated with infection compared with non-HBV-related HCC to understand interactions between viral and hepatocyte genomic alterations and their relationships with clinical features.

methodsFrozen HBV (n=86) or non-HBV-related (n=90) HCC were collected in two French surgical departments. Viral characterisation was performed by sequencing HBS and HBX genes and quantifying HBV DNA and cccDNA. Nine genes were screened for somatic mutations and expression profiling of 37 genes involved in hepatocarcinogenesis was studied.

resultsHBX revealed frequent non-sense, frameshift and deletions in tumours, suggesting an HBX inactivation selected in HCC. The number of viral copies was frequently lower in tumour than in non-tumour tissues (p=0.0005) and patients with low HBV copies in the non-tumour liver tissues presented additional risk factor (HCV, alcohol or non-alcoholic steato-hepatitis, p=0.006). P53 was the most frequently altered pathway in HBV-related HCC (47%, p=0.001). Furthermore, TP53 mutations were associated with shorter survival only in HBV-related HCC (p=0.02) whereas R249S mutations were identified exclusively in migrants. Compared with other aetiologies, HBV-HCC were more frequently classified in tumours subgroups with upregulation of genes involved in cell-cycle regulation and a progenitor phenotype. Finally, in HBV-related HCC, transcriptomic profiles were associated with specific gene mutations (HBX, TP53, IRF2, AXIN1 and CTNNB1).

conclusionsIntegrated genomic characterisation of HBV and non-HBV-related HCC emphasised the immense molecular diversity of HCC closely related to aetiologies that could impact clinical care of HCC patients.

Indexed as

AdultAgedCarcinoma, HepatocellularCohort StudiesDNA Mutational AnalysisDNA, NeoplasmFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGenomeHepatitis B, ChronicHepatitis B virusHost-Pathogen InteractionsHumansKaplan-Meier EstimateLiver NeoplasmsDNA, NeoplasmHEPATITIS BHEPATOCELLULAR CARCINOMA

Identifiers

PMID25021421
PMCPMC4392232
OpenAlexW2105327344

What OpenQuestion holds

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LicenceCC BY-NC
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.