Evidence map›Paper›PMID 37812652›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2024

Surface and Global Proteome Analyses Identify ENPP1 and Other Surface Proteins as Actionable Immunotherapeutic Targets in Ewing Sarcoma.

Brian Mooney, Gian Luca Negri, Taras Shyp, Alberto Delaidelli, Hai-Feng Zhang, Sandra E Spencer Miko, Amber K Weiner, Alexander B Radaoui, Rawan Shraim, Michael M Lizardo and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
4.6field-weighted citation impact, top 5% of its field
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

18 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
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  5. Article
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  9. Review
  10. Single-Cell RNA Sequencing of Ewing Sarcoma Tumors Demonstrates Transcriptional Heterogeneity and Clonal Evolution.Clinical cancer research : an official journal of the American Association for Cancer Research · 2025
    Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Therapeutic Hope on the Surface of Ewing Sarcoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  16. Article
  17. Review
  18. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 6 institutions in 2 countries.

Brian MooneyCanada's Michael Smith Genome Sciences Centre, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0009-0003-2834-9781
Gian Luca NegriCanada's Michael Smith Genome Sciences Centre, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0001-7722-8888
Taras ShypDepartment of Molecular Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0002-7139-3003
Alberto DelaidelliDepartment of Molecular Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0001-7416-6503
Hai-Feng ZhangDepartment of Molecular Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0001-8215-1870
Sandra E Spencer MikoCanada's Michael Smith Genome Sciences Centre, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0001-6446-1584
Amber K WeinerDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0002-2351-2936
Alexander B RadaouiDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0001-5179-7169
Rawan ShraimDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0009-0005-5350-3386
Michael M LizardoDepartment of Molecular Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0003-3981-0978
Christopher S HughesDepartment of Molecular Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0002-6980-4459
Amy LiDepartment of Molecular Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0009-0006-7752-631X
Amal M El-NaggarDepartment of Molecular Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0002-3202-6171
Melanie RouleauDepartment of Molecular Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0003-4154-3127
Wei LiDivision of Infectious Diseases, Department of Medicine, Center for Antibody Therapeutics, University of Pittsburgh Medical School, Pittsburgh, Pennsylvania.ORCID 0000-0002-6960-7404
Dimiter S DimitrovDivision of Infectious Diseases, Department of Medicine, Center for Antibody Therapeutics, University of Pittsburgh Medical School, Pittsburgh, Pennsylvania.ORCID 0000-0002-2258-1024
Raushan T KurmashevaGreehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, Texas.ORCID 0000-0003-3212-2363
Peter J HoughtonGreehey Children's Cancer Research Institute, University of Texas Health Science Center at San Antonio, San Antonio, Texas.ORCID 0000-0002-2400-8184
Sharon J DiskinDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0002-7200-8939
John M MarisDivision of Oncology and Center for Childhood Cancer Research, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.ORCID 0000-0002-8088-7929
Gregg B MorinCanada's Michael Smith Genome Sciences Centre, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0001-8949-4374
Poul H SorensenDepartment of Molecular Oncology, BC Cancer Research Institute, Vancouver, British Columbia, Canada.ORCID 0000-0001-7447-2199
BC Cancer Agency · CAChildren's Hospital of Philadelphia · USCanada's Michael Smith Genome Sciences Centre · CAThe University of Texas Health Science Center at San Antonio · USUniversity of Pittsburgh Medical Center · USUniversity of British Columbia · CA

Funding

IMMUNOBIOLOGY OF NORMAL AND NEOPLASTIC LYMPHOCYTEST32CA009140 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Malay Haldar, WARREN S PEAR · 1985 to 2026
$16.1M
Understanding and Overcoming Resistance to Immunotherapies in Childhood CancersU54CA232568 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI MACKALL, CRYSTAL, MARIS, JOHN M · 2018 to 2022
$13.1M
Discovering mechanisms of neuroblastoma tumorigenesis to improve patient outcomesR35CA220500 · NCI · CHILDREN'S HOSP OF PHILADELPHIA · PI JOHN M MARIS · 2017 to 2026
$8.7M
A Testing Program to Identify Novel Agents for Treatment of Pediatric and AYA High-Risk Sarcoma, Kidney and Liver CancerU01CA263981 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Raushan Kurmasheva · 2021 to 2026
$3.2M
NCI NIH HHS R35 CA220500NCI NIH HHS T32 CA009140NCI NIH HHS U01 CA263981NCI NIH HHS U54 CA232568
6 · The paper itself

Abstract

purposeEwing sarcoma is the second most common bone sarcoma in children, with 1 case per 1.5 million in the United States. Although the survival rate of patients diagnosed with localized disease is approximately 70%, this decreases to approximately 30% for patients with metastatic disease and only approximately 10% for treatment-refractory disease, which have not changed for decades. Therefore, new therapeutic strategies are urgently needed for metastatic and refractory Ewing sarcoma. EXPERIMENTAL

designThis study analyzed 19 unique Ewing sarcoma patient- or cell line-derived xenografts (from 14 primary and 5 metastatic specimens) using proteomics to identify surface proteins for potential immunotherapeutic targeting. Plasma membranes were enriched using density gradient ultracentrifugation and compared with a reference standard of 12 immortalized non-Ewing sarcoma cell lines prepared in a similar manner. In parallel, global proteome analysis was carried out on each model to complement the surfaceome data. All models were analyzed by Tandem Mass Tags-based mass spectrometry to quantify identified proteins.

resultsThe surfaceome and global proteome analyses identified 1,131 and 1,030 annotated surface proteins, respectively. Among surface proteins identified, both approaches identified known Ewing sarcoma-associated proteins, including IL1RAP, CD99, STEAP1, and ADGRG2, and many new cell surface targets, including ENPP1 and CDH11. Robust staining of ENPP1 was demonstrated in Ewing sarcoma tumors compared with other childhood sarcomas and normal tissues.

conclusionsOur comprehensive proteomic characterization of the Ewing sarcoma surfaceome provides a rich resource of surface-expressed proteins in Ewing sarcoma. This dataset provides the preclinical justification for exploration of targets such as ENPP1 for potential immunotherapeutic application in Ewing sarcoma. See related commentary by Bailey, p. 934.

Indexed as

Bone NeoplasmsSarcomaSarcoma, EwingAntigens, NeoplasmChildHumansImmunotherapyMembrane ProteinsOxidoreductasesProteomeProteomicsAntigens, NeoplasmMembrane ProteinsOxidoreductasesProteomeSTEAP1 protein, human

Identifiers

PMID37812652
PMCPMC10905525
OpenAlexW4387449703

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.