Evidence map›Paper›PMID 28720588›Full record

ArticleMolecular cancer research : MCR2017

EWS/FLI is a Master Regulator of Metabolic Reprogramming in Ewing Sarcoma.

Jason M Tanner, Claire Bensard, Peng Wei, Nathan M Krah, John C Schell, Jamie Gardiner, Joshua Schiffman, Stephen L Lessnick, Jared Rutter

Open access · greenAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

41 citing papers in PubMed, 52 citations in OpenAlex.

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  11. Menin in Cancer.Genes · 2024
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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

9 authors at 3 institutions in 1 country.

Jason M TannerDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, Utah.
Claire BensardDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, Utah.
Peng WeiDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, Utah.
Nathan M KrahDepartment of Human Genetics, University of Utah School of Medicine, Salt Lake City, Utah.
John C SchellDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, Utah.
Jamie GardinerDepartment of Oncological Sciences, University of Utah School of Medicine, Salt Lake City, Utah.
Joshua SchiffmanDepartment of Oncological Sciences, University of Utah School of Medicine, Salt Lake City, Utah.
Stephen L LessnickCenter for Childhood Cancer & Blood Diseases, Nationwide Children's Hospital, Columbus, Ohio.
Jared RutterDepartment of Biochemistry, University of Utah School of Medicine, Salt Lake City, Utah. rutter@biochem.utah.edu.
University of Utah · USHoward Hughes Medical Institute · USNationwide Children's Hospital · US

Funding

UTAH REGIONAL CANCER CENTERP30CA042014 · NCI · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI KATHARINE S ULLMAN · 1986 to 2026
$72.6M
Proteomics CoreU54DK110858 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Anna E Beaudin, JAMES Eric COX · 2016 to 2026
$8.6M
Genetic /Developmental Mechanisms of Pediatric DiseasesK12HD001410 · NICHD · UNIVERSITY OF UTAH · PI CLARK, EDWARD BOWERSOX · 2003 to 2012
$4.3M
Genetic Risk Factors for Ewing's SarcomaR01CA161780 · NCI · UNIVERSITY OF UTAH · PI SCHIFFMAN, JOSHUA DAVID · 2012 to 2016
$3.0M
Succinate Dehydrogenase: Biogenesis and Role in DiseaseR01GM110755 · NIGMS · UNIVERSITY OF UTAH · PI WINGE, DENNIS R. · 2014 to 2021
$2.3M
Agilent 6550 QTOF system for U of UtahS10OD016232 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2013 to 2013
$578k
Agilent 7200 GC/Q-TOF for the University of UtahS10OD021505 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2016 to 2016
$401k
A novel functional genomic pipeline for target identification in sarcomaR21CA187516 · NCI · UT SOUTHWESTERN MEDICAL CENTER · PI AMATRUDA, JAMES F, SCHIFFMAN, JOSHUA DAVID · 2014 to 2015
$377k
NCI NIH HHS P30 CA042014NCI NIH HHS R01 CA161780NCI NIH HHS R21 CA187516NICHD NIH HHS K12 HD001410NIDDK NIH HHS U54 DK110858NIGMS NIH HHS R01 GM110755NIH HHS S10 OD016232NIH HHS S10 OD021505
6 · The paper itself

Abstract

Ewing sarcoma is a bone malignancy driven by a translocation event resulting in the fusion protein EWS/FLI1 (EF). EF functions as an aberrant and oncogenic transcription factor that misregulates the expression of thousands of genes. Previous work has focused principally on determining important transcriptional targets of EF, as well as characterizing important regulatory partnerships in EF-dependent transcriptional programs. Less is known, however, about EF-dependent metabolic changes or their role in Ewing sarcoma biology. Therefore, the metabolic effects of silencing EF in Ewing sarcoma cells were determined. Metabolomic analyses revealed distinct separation of metabolic profiles in EF-knockdown versus control-knockdown cells. Mitochondrial stress tests demonstrated that knockdown of EF increased respiratory as well as glycolytic functions. Enzymes and metabolites in several metabolic pathways were altered, including

Indexed as

Bone NeoplasmsCell Line, TumorGene Expression Regulation, NeoplasticGene Knockdown TechniquesGlycolysisHumansMetabolic Networks and PathwaysMetabolomicsOncogene Proteins, FusionPhosphoglycerate DehydrogenaseProto-Oncogene Protein c-fli-1RNA-Binding Protein EWSSarcoma, EwingSignal TransductionUp-RegulationEWS-FLI fusion proteinOncogene Proteins, FusionPhosphoglycerate DehydrogenaseProto-Oncogene Protein c-fli-1RNA-Binding Protein EWS

Identifiers

PMID28720588
PMCPMC5668171
OpenAlexW2738471629

What OpenQuestion holds

Textmetadata
LicenceTDM
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.