Evidence map›Paper›PMID 33077955›Full record

ArticleNature medicine2020

Midkine rewires the melanoma microenvironment toward a tolerogenic and immune-resistant state.

Daniela Cerezo-Wallis, Marta Contreras-Alcalde, Kevin Troulé, Xavier Catena, Cynthia Mucientes, Tonantzin G Calvo, Estela Cañón, Cristina Tejedo, Paula C Pennacchi, Sabrina Hogan and 15 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

96 citing papers in PubMed, 167 citations in OpenAlex.

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  18. Spatially defined danger zone shapes gastric cancer progression through CCDC80Apoptosis : an international journal on programmed cell death · 2026
    Article
  19. Article
  20. Assessing Aβ-independent effects of Module 42 on immune function in vitro.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

25 authors at 4 institutions in 3 countries.

Daniela Cerezo-WallisMelanoma 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.
Kevin TrouléBioinformatics Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Xavier CatenaMelanoma 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.
Tonantzin G CalvoMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Estela CañónMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Cristina TejedoMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Paula C PennacchiMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Sabrina HoganDepartment of Dermatology, University of Zurich Hospital, Zurich, Switzerland.ORCID http://orcid.org/0000-0003-3994-8109
Peter KölblingerDepartment of Dermatology, University of Zurich Hospital, Zurich, Switzerland.
Héctor TejeroBioinformatics Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Andrew X ChenProgram for Mathematical Genomics, Departament of Systems Biology, Departament of Biomedical Informatics, Columbia University College of Physicians and Surgeons, New York, NY, USA.
Nuria IbarzProteomics Unit, Biotechnology Programme, Spanish National Cancer Research Centre (CNIO) and ProteoRed-ISCIII, Madrid, Madrid, Spain.
Osvaldo Graña-CastroBioinformatics Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Lola MartinezProteomics Unit, Biotechnology Programme, Spanish National Cancer Research Centre (CNIO) and ProteoRed-ISCIII, Madrid, Madrid, Spain.
Javier MuñozFlow Cytometry Unit, Biotechnology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Madrid, Spain.
Pablo Ortiz-RomeroDermatology Service, Hospital 12 de Octubre, Universidad Complutense Madrid Medical School, Madrid, Spain.ORCID http://orcid.org/0000-0003-2985-9639
José L Rodriguez-PeraltoInstituto de Investigación i+12, Hospital 12 de Octubre, Universidad Complutense Madrid Medical School, Madrid, Spain.
Gonzalo Gómez-LópezBioinformatics Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Fátima Al-ShahrourBioinformatics Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.ORCID http://orcid.org/0000-0003-2373-769X
Raúl RabadánProgram for Mathematical Genomics, Departament of Systems Biology, Departament of Biomedical Informatics, Columbia University College of Physicians and Surgeons, New York, NY, USA.ORCID http://orcid.org/0000-0001-7946-9255
Mitchell P LevesqueDepartment of Dermatology, University of Zurich Hospital, Zurich, Switzerland.
David OlmedaMelanoma Laboratory, Molecular Oncology Programme, Spanish National Cancer Research Centre (CNIO), Madrid, Spain. dolmeda@cnio.es.ORCID http://orcid.org/0000-0001-5513-5621
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
Spanish National Cancer Research Centre · ESUniversity of Zurich · CHColumbia University · USUniversidad Complutense de Madrid · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An open question in aggressive cancers such as melanoma is how malignant cells can shift the immune system to pro-tumorigenic functions. Here we identify midkine (MDK) as a melanoma-secreted driver of an inflamed, but immune evasive, microenvironment that defines poor patient prognosis and resistance to immune checkpoint blockade. Mechanistically, MDK was found to control the transcriptome of melanoma cells, allowing for coordinated activation of nuclear factor-κB and downregulation of interferon-associated pathways. The resulting MDK-modulated secretome educated macrophages towards tolerant phenotypes that promoted CD8

Indexed as

AnimalsB7-H1 AntigenCarcinogenesisCD8-Positive T-LymphocytesGene Expression Regulation, NeoplasticGenetic TherapyHumansMelanoma, ExperimentalMiceMidkineNF-kappa BProgrammed Cell Death 1 ReceptorRecombinant ProteinsTranscriptomeTumor MicroenvironmentB7-H1 AntigenCD274 protein, humanMDK protein, humanMidkineNF-kappa BProgrammed Cell Death 1 ReceptorRecombinant Proteins

Identifiers

PMID33077955
OpenAlexW3092653799

What OpenQuestion holds

Textmetadata
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.