Evidence map›Paper›PMID 41233863›Full record

ArticleJournal of translational medicine2025

Fibroblast activation protein (FAP)-mediated promotion of metastasis via the FN1-TGFβ axis and immune suppression in aggressive thyroid cancer.

Mario Udinotti, Udo Siebolts, Marcus Bauer, Christoforos Vaxevanis, Antonios Asiminas, Kerstin Lorenz, Christine Dierks, Claudia Wickenhauser, Barbara Seliger

Abstract read
In one paragraph

Article in Journal of translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Identification and assessment ofOncology letters · 2026
    Article
  2. Review
  3. FN1Oncogene · 2026
    Article
  4. Article
  5. Review
  6. Review
  7. 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

9 authors.

Mario UdinottiInstitute of Pathology, Martin Luther University Halle-Wittenberg, Halle, Germany.
Udo SieboltsInstitute of Pathology, Martin Luther University Halle-Wittenberg, Halle, Germany.
Marcus BauerInstitute of Pathology, Martin Luther University Halle-Wittenberg, Halle, Germany.
Christoforos VaxevanisInstitute of Pathology, Martin Luther University Halle-Wittenberg, Halle, Germany.
Antonios AsiminasCenter for Translational Neuromedicine, University of Copenhagen, Copenhagen, Denmark.
Kerstin LorenzDepartment of Visceral-, Vascular, and Endocrine Surgery, Martin Luther University Halle-Wittenberg, Halle, Germany.
Christine DierksDepartment of Hematology/Oncology and Stem Cell Transplantation, KIM IV, Martin-Luther University Halle-Wittenberg, Halle, Germany.
Claudia WickenhauserInstitute of Pathology, Martin Luther University Halle-Wittenberg, Halle, Germany.
Barbara SeligerInstitute of Pathology, Martin Luther University Halle-Wittenberg, Halle, Germany. barbara.seliger@uk-halle.de.ORCID 0000-0002-5544-4958

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTreatment options of aggressive thyroid carcinoma (TC) is limited due to its aggressiveness. Therefore, increased knowledge of the role of tumor intrinsic immune escape mechanisms and the microenvironment contributing to metastases formation is essential to improve the patients' outcome. These include extracellular matrix (ECM) components, cancer-associated fibroblasts (CAFs) and the expression of the fibroblast activation protein (FAP) known to be involved in immune evasion, disease progression and a worse prognosis of thyroid carcinoma (TC) patients.

methodsThe Cancer Genome Atlas (TCGA) and Human Protein Atlas datasets of TC specimens as well as tissue microarrays (TMA) consisting of 187 TC samples were analyzed for marker expression and immune cell infiltration. TC cell lines treated with recombinant FAP, a FAP inhibitor, transfected with siRNA-FAP plasmids and/or co-cultured with CAFs were subjected to qPCR, Western blot analyses and flow cytometry, cell supernatants to ELISA for cytokine secretion, the TMAs to conventional immunohistochemistry (IHC).

resultsImmunohistochemical staining and bioinformatics analyses of publicly available mRNA and protein expression profiles revealed a significant positive correlation between high FAP and fibronectin 1 (FN1) expression, metastatic parameters and CD8

conclusionsFAP-mediated alterations of ECM integrity, TC cells and CAFs underscore its potential as a powerful marker for tumor immunogenicity, immune infiltration and metastasis rendering it a promising therapeutic target for the treatment of aggressive ATC.

Indexed as

FibronectinsGelatinasesMembrane ProteinsSerine EndopeptidasesSignal TransductionThyroid NeoplasmsTransforming Growth Factor betaCancer-Associated FibroblastsCell Line, TumorEndopeptidasesFibroblast Activation Protein AlphaGene Expression Regulation, NeoplasticHumansNeoplasm MetastasisTumor MicroenvironmentEndopeptidasesFibroblast Activation Protein AlphaFibronectinsFN1 protein, humanGelatinasesMembrane ProteinsSerine EndopeptidasesTransforming Growth Factor betaCancer associated fibroblastsExtracellular matrix componentsFibroblast activating proteinImmune escapeInvasionThyroid cancerTumor microenvironment

Identifiers

PMID41233863
PMCPMC12616960

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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.