Evidence map›Paper›PMID 42355429›Full record

ArticleLife (Basel, Switzerland)2026

Genetic Profiling of Primary Versus Metastatic Ewing Sarcoma for Therapeutic Target Identification.

Carly Mitchell, Sarah Voskamp, Eddie Geagea, Deepti Anand, Jennifer Nelson, John Lovejoy

Abstract read
In one paragraph

Article in Life (Basel, Switzerland), 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

6 authors.

Carly MitchellUniversity of Central Florida College of Medicine, Orlando, FL 32827, USA.ORCID 0009-0009-6423-1776
Sarah VoskampUniversity of Central Florida College of Medicine, Orlando, FL 32827, USA.ORCID 0000-0001-8872-0712
Eddie GeageaDepartment of Orthopedics, Nemours Children's Health, Orlando, FL 32827, USA.ORCID 0009-0005-4695-7208
Deepti AnandDepartment of Research, Nemours Children's Health, Orlando, FL 32827, USA.
Jennifer NelsonUniversity of Central Florida College of Medicine, Orlando, FL 32827, USA.ORCID 0000-0001-9656-1125
John LovejoyDepartment of Orthopedics, Nemours Children's Health, Orlando, FL 32827, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ewing sarcoma (ES) is a bone malignancy primarily, well known by its t(11;22)(q24;q12) chromosomal translocation. Despite high initial treatment success, ES frequently recurs, likely due to micrometastatic disease present at diagnosis but undetected during primary treatment. This study aims to characterize transcriptomic differences between primary and metastatic ES to identify genes and pathways associated with the metastatic phenotype. Using the Search Tag Analyze Resource for National Center for Biotechnology Information's Gene Expression Omnibus, seven independent gene expression series were identified, yielding 37 metastatic and 82 primary ES tumor samples. Differentially expressed genes were defined using a significance threshold of

Indexed as

biomarkersEwing sarcomageneticsmetastasistherapeutics

Identifiers

PMID42355429
PMCPMC13302273

What OpenQuestion holds

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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.