Evidence mapPaperPMID 41708607Full record

ArticleCell death & disease2026

MLKL in liver parenchymal cells promotes liver cancer in murine metabolic dysfunction-associated steatotic liver disease.

Ghiles Imerzoukene, Ghania Hounana Kara-Ali, Céline Heitz-Marchaland, Thibaut Larcher, Mélanie Simoes Eugénio, Annaïg Hamon, Aurore Bidon, Gevorg Ghukasyan, Laurence Dubreil, Nicolas Loiseau and 6 more

Abstract read
In one paragraph

Article in Cell death & disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

16 authors.

Ghiles ImerzoukeneUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France. ghiles.imerzoukene@gmail.com.ORCID http://orcid.org/0009-0006-6814-8978
Ghania Hounana Kara-AliUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France.ORCID http://orcid.org/0000-0003-4004-7551
Céline Heitz-MarchalandUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France.
Thibaut LarcherINRAE Oniris, UMR 703 PAnTher-APEX, Nantes, France.
Mélanie Simoes EugénioUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France.
Annaïg HamonUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France.
Aurore BidonUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France.
Gevorg GhukasyanPlateforme d'Histopathologie de Haute Précision (H2P2), Université de Rennes, Rennes, France.
Laurence DubreilINRAE Oniris, UMR 703 PAnTher-APEX, Nantes, France.
Nicolas LoiseauToxalim, Université de Toulouse, INRAE, ENVT, EI-Purpan, Toulouse, France.ORCID http://orcid.org/0000-0003-3783-0879
Sarah DionUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France.
Céline Raguenes-NicolUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France.ORCID http://orcid.org/0000-0001-8428-9558
Claire Piquet-PellorceUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France.
Michel SamsonUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France.
Marie-Thérèse Dimanche-BoitrelUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France.
Jacques Le SeyecUniv Rennes, Inserm, EHESP, IRSET (Institut de recherche en santé, environnement et travail) - UMR_S, 1085, Rennes, France. jacques.leseyec@univ-rennes.fr.ORCID http://orcid.org/0000-0002-1118-3311

Funding

Fondation pour la Recherche Médicale (Foundation for Medical Research in France) DEQ20180339216Fondation pour la Recherche Médicale (Foundation for Medical Research in France) EQU202303016296Ligue Contre le Cancer Comités du Grand Ouest
6 · The paper itself

Abstract

The rising prevalence of hepatocellular carcinoma (HCC) in the last decade is mostly attributable to the growing epidemic of metabolic dysfunction-associated steatotic liver diseases (MASLD). However, the transition from steatosis to steatohepatitis (MASH) and ultimately to HCC is not fully understood. As an executioner protein of necroptosis, the mixed-lineage kinase domain-like protein (MLKL) has been proposed to contribute to MASH and HCC development. To investigate its role in disease progression, mice whose liver parenchymal cells (LPCs) no longer expressed MLKL (Mlkl

Indexed as

Carcinoma, HepatocellularFatty LiverLiverLiver NeoplasmsNon-alcoholic Fatty Liver DiseaseProtein KinasesAnimalsMaleMiceMice, Inbred C57BLMice, KnockoutNecroptosisMLKL protein, mouseProtein Kinases

Identifiers

PMID41708607
PMCPMC12920736

What Socratic 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 Socratic graph.