Evidence map›Paper›PMID 40204688›Full record

ArticleNature communications2025

Peripheral positioning of lysosomes supports melanoma aggressiveness.

Katerina Jerabkova-Roda, Marina Peralta, Kuang-Jing Huang, Antoine Mousson, Clara Bourgeat Maudru, Louis Bochler, Ignacio Busnelli, Rabia Karali, Hélène Justiniano, Lucian-Mihai Lisii and 22 more

Abstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Review
  2. Article
  3. BORC assemblies integrate BLOC-1 subunits to diversify endosomal trafficking functions.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
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

32 authors.

Katerina Jerabkova-RodaTumor Biomechanics, Strasbourg, France. katerina.jerabkova@inserm.fr.ORCID http://orcid.org/0000-0003-4734-6458
Marina PeraltaTumor Biomechanics, Strasbourg, France.
Kuang-Jing HuangTumor Biomechanics, Strasbourg, France.
Antoine MoussonUniversité de Strasbourg, Strasbourg, France.
Clara Bourgeat MaudruTumor Biomechanics, Strasbourg, France.
Louis BochlerTumor Biomechanics, Strasbourg, France.ORCID http://orcid.org/0009-0003-7050-3287
Ignacio BusnelliTumor Biomechanics, Strasbourg, France.
Rabia KaraliUniversité de Strasbourg, Strasbourg, France.
Hélène JustinianoUniversité de Strasbourg, Strasbourg, France.
Lucian-Mihai LisiiUniversité de Strasbourg, Strasbourg, France.
Philippe CarlUniversité de Strasbourg, Strasbourg, France.
Vincent MittelheisserTumor Biomechanics, Strasbourg, France.
Nandini AsokanTumor Biomechanics, Strasbourg, France.
Annabel LarnicolTumor Biomechanics, Strasbourg, France.
Olivier LefebvreTumor Biomechanics, Strasbourg, France.ORCID http://orcid.org/0000-0001-9130-9174
Hugo LachuerInstitut Curie, PSL, CNRS, UMR144, Paris, France.ORCID http://orcid.org/0000-0001-9090-7893
Angélique PichotINSERM UMR_S1109, Strasbourg, France.ORCID http://orcid.org/0000-0003-2515-5538
Tristan StemmelenINSERM UMR_S1109, Strasbourg, France.ORCID http://orcid.org/0000-0002-4382-1277
Anne MolitorINSERM UMR_S1109, Strasbourg, France.
Léa ScheidFaculté de Médecine, Université de Strasbourg et Clinique Dermatologique, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Quentin FrengerINSERM UMR_S1109, Strasbourg, France.ORCID http://orcid.org/0000-0002-2057-3813
Frédéric GrosINSERM UMR_S1109, Strasbourg, France.ORCID http://orcid.org/0000-0002-6252-4323
Aurélie HirschlerLaboratoire de Spectrométrie de Masse Bio-Organique (LSMBO), IPHC, UMR 7178, CNRS, Université de Strasbourg, Infrastructure Nationale de Protéomique ProFI, FR2048, Strasbourg, France.ORCID http://orcid.org/0000-0001-5066-6263
François DelalandeLaboratoire de Spectrométrie de Masse Bio-Organique (LSMBO), IPHC, UMR 7178, CNRS, Université de Strasbourg, Infrastructure Nationale de Protéomique ProFI, FR2048, Strasbourg, France.
Emilie SickUniversité de Strasbourg, Strasbourg, France.
Raphaël CarapitoINSERM UMR_S1109, Strasbourg, France.ORCID http://orcid.org/0000-0002-7036-442X
Christine CarapitoLaboratoire de Spectrométrie de Masse Bio-Organique (LSMBO), IPHC, UMR 7178, CNRS, Université de Strasbourg, Infrastructure Nationale de Protéomique ProFI, FR2048, Strasbourg, France.ORCID http://orcid.org/0000-0002-0079-319X
Dan LipskerFaculté de Médecine, Université de Strasbourg et Clinique Dermatologique, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Kristine Schauer *Institut Curie, PSL, CNRS, UMR144, Paris, France. kristine.schauer@gustaveroussy.fr.ORCID http://orcid.org/0000-0002-6102-8790
Philippe Rondé *Université de Strasbourg, Strasbourg, France. philippe.ronde@unistra.fr.
Vincent Hyenne *Tumor Biomechanics, Strasbourg, France. hyenne@unistra.fr.ORCID http://orcid.org/0000-0002-1254-2814
Jacky G Goetz *Tumor Biomechanics, Strasbourg, France. jacky.goetz@inserm.fr.ORCID http://orcid.org/0000-0003-2842-8116

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Emerging evidence suggests that the function and position of organelles are pivotal for tumor cell dissemination. Among them, lysosomes stand out as they integrate metabolic sensing with gene regulation and secretion of proteases. Yet, how their function is linked to their position and how this controls metastasis remains elusive. Here, we analyze lysosome subcellular distribution in patient-derived melanoma cells and patient biopsies and show that lysosome spreading scales with melanoma aggressiveness. Peripheral lysosomes promote matrix degradation and cell invasion which is directly linked to the lysosomal and cell transcriptional programs. Using chemo-genetical control of lysosome positioning, we demonstrate that perinuclear clustering impairs lysosome secretion, matrix degradation and invasion. Impairing lysosome spreading significantly reduces invasive outgrowth in two in vivo models, mouse and zebrafish. Our study provides a direct demonstration that lysosome positioning controls cell invasion, illustrating the importance of organelle adaptation in carcinogenesis and suggesting its potential utility for diagnosis of metastatic melanoma.

Indexed as

LysosomesMelanomaSkin NeoplasmsAnimalsCell Line, TumorFemaleHumansMiceNeoplasm InvasivenessZebrafish

Identifiers

PMID40204688
PMCPMC11982396

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.