Evidence map›Paper›PMID 42088348›Full record

ArticleiScience2026

Immune infiltration is associated with distinct transcriptional states and metabolic profiles in chordomas.

Siddh van Oost, Rick Ursem, Zeynep B Erdem, Sara Cardoso, Sanne Venneker, Ruud van der Breggen, Inge H Briaire-de Bruijn, Alwine B Kruisselbrink, Wilco C Peul, Karoly Szuhai and 5 more

Abstract read
In one paragraph

Article in iScience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Siddh van OostDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Rick UrsemDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Zeynep B ErdemDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Sara CardosoDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Sanne VennekerDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Ruud van der BreggenDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Inge H Briaire-de BruijnDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Alwine B KruisselbrinkDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Wilco C PeulUniversity Neurosurgical Center Holland, Leiden University Medical Center, Leiden, the Netherlands.
Karoly SzuhaiDepartment of Cell & Chemical Biology, Leiden University Medical Center, Leiden, the Netherlands.
Robert J P van der WalDepartment of Orthopedic Surgery, Leiden University Medical Center, Leiden, the Netherlands.
Rene van ZeijlCenter of Proteomics & Metabolomics, Leiden University Medical Center, Leiden, the Netherlands.
Bram HeijsCenter of Proteomics & Metabolomics, Leiden University Medical Center, Leiden, the Netherlands.
Noel F C C de MirandaDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.
Judith V M G BoveeDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chordomas are ultra-rare malignancies of the axial skeleton with limited treatment options. Some tumors exhibit immunogenic features and respond to checkpoint blockade, but the biological determinants remain unclear. To investigate chordoma immunogenicity, we integrated spatial transcriptomic and metabolomic profiling. GeoMx digital spatial profiling was performed on 15 chordomas, analyzing tumor and stromal compartments and comparing inflamed versus non-inflamed tumors. Consecutive sections underwent MALDI mass spectrometry imaging. Key findings were validated by immunohistochemistry. To link transcriptional states with interferon-γ, chordoma cell lines were treated with interferon-γ. Spatial profiling revealed transcriptomic differences between inflamed and non-inflamed tumors across both compartments, and immune infiltration correlated with a broader gene expression repertoire in cancer cells. MSI identified distinct metabolic signatures, including glycogen accumulation in inflamed tumors. However, interferon-γ treatment did not induce

Indexed as

health sciencesimmunologymedicine

Identifiers

PMID42088348
PMCPMC13137147

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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.