Evidence map›Paper›PMID 34439098›Full record

ArticleCancers2021

CCL20/TNF/VEGFA Cytokine Secretory Phenotype of Tumor-Associated Macrophages Is a Negative Prognostic Factor in Cutaneous Melanoma.

Alba Gutiérrez-Seijo, Elena García-Martínez, Celia Barrio-Alonso, Miriam Pareja-Malagón, Alejandra Acosta-Ocampo, María Eugenia Fernández-Santos, Amaya Puig-Kröger, Verónica Parra-Blanco, Enrique Mercader, Iván Márquez-Rodas and 3 more

Abstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. The tumor immune microenvironment in primary cutaneous melanoma.Archives of dermatological research · 2025
    Review
  6. Article
  7. Article
  8. Review
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  12. Article
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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

13 authors.

Alba Gutiérrez-SeijoUnidad de Microscopía Confocal, Instituto de Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.ORCID 0000-0001-6282-3932
Elena García-MartínezUnidad de Microscopía Confocal, Instituto de Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.ORCID 0000-0001-8211-4287
Celia Barrio-AlonsoUnidad de Microscopía Confocal, Instituto de Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.ORCID 0000-0002-2789-1363
Miriam Pareja-MalagónUnidad de Producción Celular, Instituto Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.ORCID 0000-0003-2908-823X
Alejandra Acosta-OcampoUnidad de Producción Celular, Instituto Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.
María Eugenia Fernández-SantosUnidad de Producción Celular, Instituto Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.
Amaya Puig-KrögerLaboratorio de Inmuno-Metabolismo e Inflamación, Instituto de Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.
Verónica Parra-BlancoServicio de Anatomía Patológica, Hospital General Universitario Gregorio Marañón, 28007 Madrid, Spain.ORCID 0000-0002-7916-5478
Enrique MercaderUnidad Cirugía Endocrino-Metabólica, Servicio de Cirugía General y Aparato Digestivo, Hospital General Universitario Gregorio Marañón, Calle Doctor Esquerdo 46, 28007 Madrid, Spain.ORCID 0000-0002-1836-0165
Iván Márquez-RodasServicio de Oncología Médica, Hospital General Universitario Gregorio Marañón, 28007 Madrid, Spain.
José Antonio Avilés-IzquierdoServicio de Dermatología, Hospital General Universitario Gregorio Marañón, 28007 Madrid, Spain.
Rafael SamaniegoUnidad de Microscopía Confocal, Instituto de Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.ORCID 0000-0002-3081-7332
Paloma Sánchez-MateosLaboratorio de Inmuno-Oncología, Instituto de Investigación Sanitaria Gregorio Marañón, 28007 Madrid, Spain.

Funding

Cancer Research UK, FCAECC and AIRC Accelerator Award GCB15152947MELEMinisterio de Economía y Competitividad PI17/01324
6 · The paper itself

Abstract

TAMs constitute a large fraction of infiltrating immune cells in melanoma tissues, but their significance for clinical outcomes remains unclear. We explored diverse TAM parameters in clinically relevant primary cutaneous melanoma samples, including density, location, size, and polarization marker expression; in addition, because cytokine production is a hallmark of macrophages function, we measured CCL20, TNF, and VEGFA intracellular cytokines by single-cell multiparametric confocal microscopy. The Kaplan-Meier method was used to analyze correlation with melanoma-specific disease-free survival and overall survival. No significant correlations with clinical parameters were observed for TAM density, morphology, or location. Significantly, higher contents of the intracellular cytokines CCL20, TNF, and VEGFA were quantified in TAMs infiltrating metastasizing compared to non-metastasizing skin primary melanomas (

Indexed as

biomarkerCCL20melanomametastasisprognostic factorTAMTNFVEGFA

Identifiers

PMID34439098
PMCPMC8392234

What OpenQuestion holds

Textmetadata
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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.