Evidence map›Paper›PMID 39924882›Full record

ArticlePigment cell & melanoma research2025

A Unique Signature for Cancer-Associated Fibroblasts in Melanoma Metastases.

Saskia Tauch, Joschka Hey, Bettina Kast, Nicolas Gengenbacher, Lena Weiß, Melanie Sator-Schmitt, Sabrina Lohr, Alexander Brobeil, Peter Schirmacher, Jochen Utikal and 3 more

Abstract read
In one paragraph

Article in Pigment cell & melanoma research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
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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.

Saskia TauchDivision Signal Transduction and Growth Control, German Cancer Research Center (DKFZ-ZMBH Alliance), Heidelberg, Germany.
Joschka HeyDivision of Cancer Epigenomics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Bettina KastDivision Signal Transduction and Growth Control, German Cancer Research Center (DKFZ-ZMBH Alliance), Heidelberg, Germany.
Nicolas GengenbacherDivision of Vascular Oncology and Metastasis, German Cancer Research Center (DKFZ-ZMBH Alliance), Heidelberg, Germany.
Lena WeißDivision Signal Transduction and Growth Control, German Cancer Research Center (DKFZ-ZMBH Alliance), Heidelberg, Germany.
Melanie Sator-SchmittDivision Signal Transduction and Growth Control, German Cancer Research Center (DKFZ-ZMBH Alliance), Heidelberg, Germany.
Sabrina LohrDivision Signal Transduction and Growth Control, German Cancer Research Center (DKFZ-ZMBH Alliance), Heidelberg, Germany.
Alexander BrobeilInstitute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Peter SchirmacherInstitute of Pathology, University Hospital Heidelberg, Heidelberg, Germany.
Jochen UtikalDKFZ-Hector Cancer Institute, University Medical Centre Mannheim, Mannheim, Germany.
Hellmut G AugustinDivision of Vascular Oncology and Metastasis, German Cancer Research Center (DKFZ-ZMBH Alliance), Heidelberg, Germany.
Christoph PlassDivision of Cancer Epigenomics, German Cancer Research Center (DKFZ), Heidelberg, Germany.
Peter AngelDivision Signal Transduction and Growth Control, German Cancer Research Center (DKFZ-ZMBH Alliance), Heidelberg, Germany.ORCID 0000-0001-8234-5587

Funding

Deutsche Forschungsgemeinschaft 259332240/RTG 2099
6 · The paper itself

Abstract

Cancer-associated fibroblasts (CAFs) represent a central cell population of the tumor microenvironment (TME). Recently, single-cell RNA-sequencing (scRNA-seq) analyses of primary tumors of different cancer entities yielded different classifications of CAF subsets underscoring the heterogeneity of CAFs within the TME. Here, we analyzed the transcriptional signatures of approximately 8400 CAFs and normal fibroblasts by scRNA-seq and compared genetic profiles of CAFs from murine melanoma primary tumors to CAFs from corresponding melanoma lung metastases. This revealed distinct subsets for primary tumor and metastasis-specific CAF populations, respectively. Combined with the spatial characterization of metastasis CAFs at the RNA and protein level, scRNA analyses indicate tumor-dependent crosstalk between neutrophils and CAFs, mediated via SAA3 and IL1b-related signaling pathways, which can be recapitulated in vitro. Analyzing tissue sections of human patient samples, this interaction was found to be present in human melanoma metastasis. Taken together, our data highlight unique characteristics of metastasis CAFs with potential therapeutic impact for melanoma metastasis.

Indexed as

Cancer-Associated FibroblastsMelanomaSkin NeoplasmsAnimalsCell Line, TumorGene Expression Regulation, NeoplasticHumansMiceNeoplasm MetastasisSignal TransductionSingle-Cell AnalysisTumor MicroenvironmentCAFmelanomametastasisSAAscRNA sequencing

Identifiers

PMID39924882
PMCPMC11808227

What OpenQuestion holds

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LicenceCC BY
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.