Evidence map›Paper›PMID 40858520›Full record

ArticleCancer research communications2025

TGFβ Inhibition during Radiotherapy Enhances Immune Cell Infiltration and Decreases Metastases in Ewing Sarcoma.

Jessica D Daley, Elina Mukherjee, David Ferraro, A Carolina Tufino, Nathanael Bailey, Shanthi Bhaskar, Nivitha Periyapatna, Ian MacFawn, Sean Hartwick, Sheryl Kunning and 9 more

Abstract read
In one paragraph

Article in Cancer research communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

19 authors.

Jessica D DaleyDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0001-5133-448X
Elina MukherjeeDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0001-9750-7219
David FerraroDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0009-0004-2849-4353
A Carolina TufinoDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0009-0000-8585-1063
Nathanael BaileyDepartment of Pathology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0002-6747-680X
Shanthi BhaskarDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0009-0009-0598-1673
Nivitha PeriyapatnaDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0009-0000-9348-9551
Ian MacFawnUPMC Hillman Cancer Center, Pittsburgh, Pennsylvania.ORCID 0000-0001-9056-1255
Sean HartwickDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0009-0006-2474-5623
Sheryl KunningDepartment of Immunology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0001-7529-040X
Cynthia HinckDepartment of Structural Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0002-2163-9378
Tullia C BrunoUPMC Hillman Cancer Center, Pittsburgh, Pennsylvania.ORCID 0000-0002-6433-0207
Adam C OlsonDepartment of Radiation Oncology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0002-0771-9486
Linda M McAllister-LucasDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0002-9875-5043
Andrew P HinckDepartment of Structural Biology, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0003-3320-8054
Kristine CooperUPMC Hillman Cancer Center Biostatistics Facility, Pittsburgh, Pennsylvania.ORCID 0000-0002-8172-1648
Riyue BaoUPMC Hillman Cancer Center, Pittsburgh, Pennsylvania.ORCID 0000-0002-6105-1704
Anthony R CilloUPMC Hillman Cancer Center, Pittsburgh, Pennsylvania.ORCID 0000-0002-3213-3129
Kelly M BaileyDepartment of Pediatrics, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania.ORCID 0000-0003-3925-3243

Funding

VECTOR CORE FACILITYP30CA047904 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI CHRISTOPHER J. BAKKENIST · 1988 to 2026
$158.0M
Molecular Basis of Pediatric DiseaseK12HD052892 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TERENCE S. DERMODY · 2007 to 2026
$6.5M
Research Training Program for Pediatric Subspecialty FellowsT32HD071834 · NICHD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI TERENCE S. DERMODY · 2013 to 2026
$4.7M
DNA Damage and Immunogenicity in Ewing SarcomaK08CA252178 · NCI · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BAILEY, KELLY · 2021 to 2025
$765k
High-Throughput Computing for Genomics and Bioinformatics ResearchS10OD028483 · OD · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI LEE, ADRIAN V · 2021 to 2021
$574k
Alex's Lemonade Stand Foundation for Childhood Cancer (ALSF) Young Investigator AwardBurroughs Wellcome Fund (BWF)National Institutes of Health (NIH) K12HD052892-15National Institutes of Health (NIH) T32HD071834NCI NIH HHS K08 CA252178NCI NIH HHS P30 CA047904NICHD NIH HHS K12 HD052892NICHD NIH HHS T32 HD071834NIH HHS S10 OD028483UPMC Children's Foundation N/A
6 · The paper itself

Abstract

Ewing sarcoma is an aggressive cancer diagnosed in adolescents and young adults. Inhibition of TGFβ is being tested in limited clinical trials for relapsed Ewing sarcoma. TGFβ is an immunosuppressive cytokine that exists in latent and active states. The functional impact of TGFβ inhibition on the Ewing tumor microenvironment (TME) and on Ewing tumor behavior remains largely unknown. In this study, we use single-cell RNA sequencing analysis of human Ewing tumors to demonstrate that immune cells are the largest contributors of TGFB1 expression in the human Ewing TME. We utilize a humanized mouse model of Ewing sarcoma to demonstrate that TME signatures in these models differ significantly from Ewing sarcoma tumors developed in immunodeficient mice. Using this humanized model, we investigate the effect of TGFβ inhibition on the Ewing sarcoma TME during radiotherapy, a treatment that is commonly used to treat unresectable, metastatic, and relapsed/refractory Ewing sarcoma that is known to enhance TGFβ activation in multiple cancers. Utilizing a trivalent ligand TGFβ trap to inhibit TGFβ, we demonstrate that in combination with radiotherapy, TGFβ inhibition both increases Ewing sarcoma immune cell infiltration and decreases lung metastatic burden in vivo. These data demonstrate the value of immunocompetent models to address immune-biological preclinical questions in Ewing sarcoma and demonstrate that TGFβ inhibition during radiotherapy is a promising strategy to enhance antitumor immune response and improve treatment efficacy for metastatic Ewing sarcoma. SIGNIFICANCE: This work demonstrates the importance of disrupting immunosuppression during radiotherapy to reduce lung metastatic potential in Ewing sarcoma. Humanized mouse models of Ewing sarcoma are also established as an immunocompetent preclinical tool to ask therapeutic questions about the Ewing TME.

Indexed as

Bone NeoplasmsLung NeoplasmsSarcoma, EwingTransforming Growth Factor betaTransforming Growth Factor beta1AnimalsCell Line, TumorFemaleHumansMiceTumor MicroenvironmentXenograft Model Antitumor AssaysTransforming Growth Factor betaTransforming Growth Factor beta1

Identifiers

PMID40858520
PMCPMC12380665

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.