Evidence map›Paper›PMID 40155713›Full record

ArticleNature cancer2025

Systemic rewiring of dendritic cells by melanoma-secreted midkine impairs immune surveillance and response to immune checkpoint blockade.

Xavier Catena, Marta Contreras-Alcalde, Naiara Juan-Larrea, Daniela Cerezo-Wallis, Tonantzin G Calvo, Cynthia Mucientes, David Olmeda, Javier Suárez, Sergio Oterino-Sogo, Lola Martínez and 8 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature cancer, 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. Article
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  4. Review
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  8. Ageing, immune fitness and cancer.Nature reviews. Cancer · 2025
    Review
  9. Review
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  11. Article
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

18 authors.

Xavier CatenaMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Marta Contreras-AlcaldeMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Naiara Juan-LarreaMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.ORCID http://orcid.org/0000-0001-6088-5507
Daniela Cerezo-WallisMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Tonantzin G CalvoMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Cynthia MucientesMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
David OlmedaMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.ORCID http://orcid.org/0000-0001-5513-5621
Javier SuárezMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Sergio Oterino-SogoMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.ORCID http://orcid.org/0000-0002-6461-4031
Lola MartínezFlow Cytometry Core Unit, Biotechnology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Diego MegíasAdvanced Optical Microscopy Unit, Instituto de Salud Carlos III (ISCIII), Majadahonda, Spain.ORCID http://orcid.org/0000-0003-0755-0518
David SanchoImmunobiology Lab, Centro Nacional de Investigación Cardiovasculares (CNIC), Madrid, Spain.ORCID http://orcid.org/0000-0003-2890-3984
Cristina TejedoMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Susana FragoMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Diana DudziakInstitute of Immunology, Jena University Hospital, Friedrich-Schiller-University, Jena, Germany.
Athanasios SeretisDepartment of Dermatology, Venereology and Allergology, Medical University of Innsbruck, Innsbruck, Austria.ORCID http://orcid.org/0000-0003-1529-3507
Patrizia StoitznerDepartment of Dermatology, Venereology and Allergology, Medical University of Innsbruck, Innsbruck, Austria.
María S SoengasMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain. msoengas@cnio.es.ORCID http://orcid.org/0000-0003-0612-6299

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) TRR305-TPB5 429280966EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 884699EC | European Regional Development Fund (Europski Fond za Regionalni Razvoj) PI21/00641EC | Horizon 2020 Framework Programme (EU Framework Programme for Research and Innovation H2020) 641549"la Caixa" Foundation (Caixa Foundation) HR20-00465"la Caixa" Foundation (Caixa Foundation) LCF/PR/HR23/52430012Ministerio de Educación, Cultura y Deporte (Ministry of Education, Culture and Sports, Spain) MCIN/AEI/10.13039/501100011033Ministerio de Educación, Cultura y Deporte (Ministry of Education, Culture and Sports, Spain) PID2020-117621RB-I00Ministry of Economy and Competitiveness | Instituto de Salud Carlos III (Institute of Health Carlos III) AES-2021
6 · The paper itself

Abstract

Cutaneous melanomas express a high number of potential neoepitopes, yet a substantial fraction of melanomas shift into immunologically cold phenotypes. Using cellular systems, mouse models and large datasets, we identify the tumor-secreted growth factor midkine (MDK) as a multilayered inhibitor of antigen-presenting cells. Mechanistically, MDK acts systemically in primary tumors, lymph nodes and the bone marrow, promoting a STAT3-mediated impairment of differentiation, activation and function of dendritic cells (DCs), particularly, conventional type 1 DCs (cDC1s). Furthermore, MDK rewires DCs toward a tolerogenic state, impairing CD8

Indexed as

Dendritic CellsImmune Checkpoint InhibitorsMelanomaMidkineSkin NeoplasmsAnimalsCD8-Positive T-LymphocytesCell Line, TumorFemaleHumansMiceMice, Inbred C57BLSTAT3 Transcription FactorImmune Checkpoint InhibitorsMDK protein, humanMidkineSTAT3 Transcription Factor

Identifiers

PMID40155713

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.