Evidence map›Paper›PMID 41922083›Full record

ArticleJournal for immunotherapy of cancer2026

Epigenetic remodeling in sarcoma promotes T-cell infiltration via modulation of the Hippo pathway.

Mireia Cruz De Los Santos, Yi Chen, Amaia González De Zárate, Agnes Sorteberg, Honglei Zhao, Guillermo Vázquez-Cabrera, Neda Bigdeli, Solrun Kolbeinsdottir, Aarren Mannion, Lucas Baldran-Groves and 7 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

17 authors.

Mireia Cruz De Los SantosDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden Andreas.Lundqvist@ki.se mireia.cruz.de.los.santos@ki.se.ORCID http://orcid.org/0000-0001-8349-8366
Yi ChenDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Amaia González De ZárateDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Agnes Sorteberg *Department of Women's, and Children's Health,Childhood Cancer Research Unit, Karolinska Institutet, Solna, Sweden.
Honglei Zhao *Department of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Guillermo Vázquez-CabreraInstitute of Environmental Medicine, Toxicology Unit, Karolinska Institutet, Solna, Sweden.ORCID http://orcid.org/0000-0003-1708-6712
Neda BigdeliDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Solrun KolbeinsdottirDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0001-7462-0278
Aarren MannionDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-1837-986X
Lucas Baldran-GrovesDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0009-0006-5555-378X
Shi Yong NeoSingapore Immunology Network, Agency for Science, Technology and Research, A*STAR, Singapore.
Stina Linnea WickströmDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0003-0349-4918
Jeroen MeliefDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0003-4108-5437
Lars HolmgrenDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Nikolas HeroldDepartment of Women's, and Children's Health,Childhood Cancer Research Unit, Karolinska Institutet, Solna, Sweden.ORCID http://orcid.org/0000-0001-9468-4543
Felix Haglund de FlonDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden.
Andreas LundqvistDepartment of Oncology-Pathology, Karolinska Institutet, Stockholm, Sweden Andreas.Lundqvist@ki.se mireia.cruz.de.los.santos@ki.se.ORCID http://orcid.org/0000-0002-9709-2970

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInsufficient T-cell infiltration limits the effectiveness of immunotherapy in sarcoma, yet the tumor-intrinsic mechanisms that govern immune exclusion remain poorly defined.

methodsBy integrating patient-derived ex vivo sarcoma spheroids with autologous expanded tumor-infiltrating lymphocytes and an in vivo metastatic osteosarcoma model, antitumor immune regulation by histone modifications was examined.

resultsHistone H3 lysine 27 acetylation (H3K27ac) was identified as a key regulator of CD8

conclusionsOur findings reveal an epigenetic-Hippo-immunomodulatory axis in osteosarcoma that also extends to other sarcomas, providing a rationale for incorporating epigenetic preconditioning with immunotherapy to improve patient outcomes and pointing towards novel biomarkers for treatment guidance.

Indexed as

Epigenesis, GeneticHippo Signaling PathwayLymphocytes, Tumor-InfiltratingSarcomaAnimalsHistonesHumansMiceHistonesImmunotherapyMemorySarcomaT cellTumor infiltrating lymphocyte - TIL

Identifiers

PMID41922083
PMCPMC13052610

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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.