Evidence map›Paper›PMID 35285802›Full record

ArticleeLife2022

Dysregulated heparan sulfate proteoglycan metabolism promotes Ewing sarcoma tumor growth.

Elena Vasileva, Mikako Warren, Timothy J Triche, James F Amatruda

Open access · goldAbstract read
In one paragraph

Article in eLife, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 34 citations in OpenAlex.

  1. A Drosophila Study Model for EWS::FLI1-Induced Molecular Pathways.Methods in molecular biology (Clifton, N.J.) · 2027
    Article
  2. Tissue-Specific Expression of the EWSR1::FLI1 Fusion Protein IdentifiesInternational journal of molecular sciences · 2026
    Article
  3. Review
  4. Article
  5. Choosing the right animal model for sarcoma research.Cellular and molecular life sciences : CMLS · 2026
    Review
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Therapeutic Hope on the Surface of Ewing Sarcoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  13. Review
  14. Seed Becoming Soil: A New Paradigm of the Ewing Sarcoma Tumor Microenvironment.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Article
  15. Article
  16. Article
  17. Article
  18. Fli1 and Tissue Fibrosis in Various Diseases.International journal of molecular sciences · 2023
    Review
  19. Review
  20. 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

4 authors at 2 institutions in 1 country.

Elena VasilevaCancer and Blood Disease Institute, Children's Hospital Los Angeles, Los Angeles, United States.ORCID 0000-0003-2026-1331
Mikako WarrenDivision of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, United States.
Timothy J TricheDivision of Pathology and Laboratory Medicine, Children's Hospital Los Angeles, Los Angeles, United States.
James F AmatrudaCancer and Blood Disease Institute, Children's Hospital Los Angeles, Los Angeles, United States.ORCID 0000-0002-9901-2137
University of Southern California · USChildren's Hospital of Los Angeles · US

Funding

Targeting EWSR1-FLI1 through Functional, Structural and Chemical ApproachesU54CA231649 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI AMATRUDA, JAMES F, MCFADDEN, DAVID GLENN · 2019 to 2019
$10.0M
NCI NIH HHS U54 CA231649
6 · The paper itself

Abstract

The Ewing sarcoma family of tumors is a group of malignant small round blue cell tumors (SRBCTs) that affect children, adolescents, and young adults. The tumors are characterized by reciprocal chromosomal translocations that generate chimeric fusion oncogenes, the most common of which is EWSR1-FLI1. Survival is extremely poor for patients with metastatic or relapsed disease, and no molecularly targeted therapy for this disease currently exists. The absence of a reliable genetic animal model of Ewing sarcoma has impaired investigation of tumor cell/microenvironmental interactions in vivo. We have developed a new genetic model of Ewing sarcoma based on Cre-inducible expression of human

Indexed as

Sarcoma, EwingAdolescentAnimalsHeparan Sulfate ProteoglycansHumansOncogene Proteins, FusionRNA-Binding Protein EWSZebrafishHeparan Sulfate ProteoglycansOncogene Proteins, FusionRNA-Binding Protein EWScancercancer biologyEwing sarcomaextracellular matrixproteoglycansSurfenzebrafish

Identifiers

PMID35285802
PMCPMC8942468
OpenAlexW4220875532

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.