Evidence map›Paper›PMID 40097385›Full record

ArticleCell death discovery2025

Role of TRIM24 in the regulation of proteasome-autophagy crosstalk in bortezomib-resistant mantle cell lymphoma.

Corentin Bouvier, Maria Gonzalez-Santamarta, Núria Profitós-Pelejà, Marc Armengol, Grégoire Quinet, Quentin Alasseur, Laurie Ceccato, Wendy Xolalpa, Raimundo Freire, Julie Guillermet-Guibert and 10 more

Abstract read
In one paragraph

Article in Cell death discovery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Trial
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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

20 authors.

Corentin Bouvier *Laboratoire de Chimie de Coordination (LCC) CNRS-UPR8241, Toulouse, 31077, France.ORCID http://orcid.org/0000-0002-3344-6856
Maria Gonzalez-Santamarta *Laboratoire de Chimie de Coordination (LCC) CNRS-UPR8241, Toulouse, 31077, France.
Núria Profitós-Pelejà *Lymphoma Translational Group, UBIRed, Josep Carreras Leukaemia Research Institute, 08916, Badalona, Spain.
Marc ArmengolLymphoma Translational Group, UBIRed, Josep Carreras Leukaemia Research Institute, 08916, Badalona, Spain.
Grégoire QuinetUnidad de Investigación, Hospital Universitario de Canarias, Instituto de Investigación Sanitaria de Canarias (IISC), La Laguna, La Laguna, Santa Cruz de Tenerife, Spain.
Quentin AlasseurBMolecular, Centre Pierre Potier, Toulouse, 31100, France.
Laurie CeccatoLaboratoire de Chimie de Coordination (LCC) CNRS-UPR8241, Toulouse, 31077, France.
Wendy XolalpaDepartamento de Ingeniería Celular y Biocatálisis, Instituto de Biotecnología, UNAM, 62210, Cuernavaca, Morelos, Mexico.
Raimundo FreireUnidad de Investigación, Hospital Universitario de Canarias, Instituto de Investigación Sanitaria de Canarias (IISC), La Laguna, La Laguna, Santa Cruz de Tenerife, Spain.ORCID http://orcid.org/0000-0003-4473-8894
Julie Guillermet-GuibertCentre de Recherche en Cancerologie de Toulouse (CRCT), Inserm, CNRS, Université de Toulouse, Toulouse, 31100, France.ORCID http://orcid.org/0000-0003-3173-4907
Karine ReybierPharmaDev, UMR 152, Université de Toulouse, IRD, UT3, 31400, Toulouse, France.
Anne-Marie CaminadeLaboratoire de Chimie de Coordination (LCC) CNRS-UPR8241, Toulouse, 31077, France.
Hans C BeckDepartment of Clinical Biochemistry, Odense University Hospital, Odense, Denmark.
Ana Sofia CarvalhoComputational and Experimental Biology Group, iNOVA4Health, Nova Medical School, Facultade de Ciências Médicas, Universidade Nova de Lisboa, 1150-082, Lisboa, Portugal.
Rune MatthiesenComputational and Experimental Biology Group, iNOVA4Health, Nova Medical School, Facultade de Ciências Médicas, Universidade Nova de Lisboa, 1150-082, Lisboa, Portugal.
Jean Christophe RainHybrigenics Services, 1 rue Pierre Fontaine, 91000, Evry Genopole, France.
James D SutherlandCenter for Cooperative Research in Biosciences (CIC bioGUNE), Basque Research and Technology Alliance (BRTA), Bizkaia Technology Park, Building 801A, 48160, Derio, Spain.ORCID http://orcid.org/0000-0003-3229-793X
Rosa BarrioCenter for Cooperative Research in Biosciences (CIC bioGUNE), Basque Research and Technology Alliance (BRTA), Bizkaia Technology Park, Building 801A, 48160, Derio, Spain.ORCID http://orcid.org/0000-0002-9663-0669
Gaël RouéLymphoma Translational Group, UBIRed, Josep Carreras Leukaemia Research Institute, 08916, Badalona, Spain. groue@carrerasresearch.org.ORCID http://orcid.org/0000-0003-0245-2257
Manuel S RodriguezLaboratoire de Chimie de Coordination (LCC) CNRS-UPR8241, Toulouse, 31077, France. manuel.rodriguez@lcc-toulouse.fr.ORCID http://orcid.org/0000-0001-5445-4495

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Resistance to bortezomib (BTZ) represents a major bottleneck to continue using this proteasome inhibitor in the treatment of mantle cell lymphoma (MCL). In this study, we investigated the mechanisms by which TRIM24 (tripartite motif-containing 24), a ubiquitin ligase enriched in the ubiquitome of BTZ-resistant MCL cells, modulates proteasome-autophagy crosstalk. The localization and stability of TRIM24 were differentially influenced by the inhibition of proteasome or autophagy in MCL cells with acquired BTZ resistance (ZBR). Moreover, genetic deletion of the TRIM24 gene in ZBR (ZBR

Identifiers

PMID40097385
PMCPMC11914149

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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.