Evidence map›Paper›PMID 37968277›Full record

ArticleNature communications2023

PAX3-FOXO1 dictates myogenic reprogramming and rhabdomyosarcoma identity in endothelial progenitors.

Madeline B Searcy, Randolph K Larsen, Bradley T Stevens, Yang Zhang, Hongjian Jin, Catherine J Drummond, Casey G Langdon, Katherine E Gadek, Kyna Vuong, Kristin B Reed and 11 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 29 citations in OpenAlex.

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  17. PAX Family, Master Regulator in Cancer.Diagnostics (Basel, Switzerland) · 2025
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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

21 authors at 2 institutions in 1 country.

Madeline B Searcy *Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Randolph K Larsen *Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Bradley T StevensDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Yang ZhangDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Hongjian JinCenter for Applied Bioinformatics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Catherine J DrummondDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Casey G LangdonDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0002-0010-7209
Katherine E GadekDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0001-5170-230X
Kyna VuongDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Kristin B ReedDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0003-0595-9096
Matthew R GarciaDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Beisi XuCenter for Applied Bioinformatics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0003-0099-858X
Darden W KimbroughDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Grace E AdkinsDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Nadhir DjekidelCenter for Applied Bioinformatics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0001-5361-1858
Shaina N PorterDepartment of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Patrick A SchreinerDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0001-5391-2642
Shondra M Pruett-MillerDepartment of Cell and Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0002-3793-585X
Brian J AbrahamDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0001-8085-3027
Jerold E RehgDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Mark E HatleyDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA. mark.hatley@stjude.org.ORCID 0000-0001-7147-3946
St. Jude Children's Research Hospital · USRhodes College · US

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI SUZANNE J. BAKER · 1985 to 2026
$166.9M
Defining the non-myogenic origins of pediatric rhabdomyosarcomaR01CA216344 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI HATLEY, MARK EDWARD · 2017 to 2021
$2.0M
Mediators Of Arrested Differentiation In Pediatric RhabdomyosarcomaR01CA251436 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI HATLEY, MARK EDWARD · 2021 to 2025
$2.0M
Determining the Mechanism of Transformation for RhabdomyosarcomaF31CA250398 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL GRADUATE SCHOOL OF BIOMEDICAL SCIENCES, LLC · PI SEARCY, MADELINE BUSH · 2021 to 2022
$85k
NCI NIH HHS F31 CA250398NCI NIH HHS P30 CA021765NCI NIH HHS R01 CA216344NCI NIH HHS R01 CA251436
6 · The paper itself

Abstract

Fusion-positive rhabdomyosarcoma (FP-RMS) driven by the expression of the PAX3-FOXO1 (P3F) fusion oncoprotein is an aggressive subtype of pediatric rhabdomyosarcoma. FP-RMS histologically resembles developing muscle yet occurs throughout the body in areas devoid of skeletal muscle highlighting that FP-RMS is not derived from an exclusively myogenic cell of origin. Here we demonstrate that P3F reprograms mouse and human endothelial progenitors to FP-RMS. We show that P3F expression in aP2-Cre expressing cells reprograms endothelial progenitors to functional myogenic stem cells capable of regenerating injured muscle fibers. Further, we describe a FP-RMS mouse model driven by P3F expression and Cdkn2a loss in endothelial cells. Additionally, we show that P3F expression in TP53-null human iPSCs blocks endothelial-directed differentiation and guides cells to become myogenic cells that form FP-RMS tumors in immunocompromised mice. Together these findings demonstrate that FP-RMS can originate from aberrant development of non-myogenic cells driven by P3F.

Indexed as

RhabdomyosarcomaRhabdomyosarcoma, AlveolarAnimalsCell Line, TumorChildEndothelial CellsForkhead Box Protein O1Gene Expression Regulation, NeoplasticHumansMiceMuscle, SkeletalOncogene Proteins, FusionPaired Box Transcription FactorsPAX3 Transcription FactorForkhead Box Protein O1FOXO1 protein, humanFoxo1 protein, mouseOncogene Proteins, FusionPaired Box Transcription FactorsPAX3 protein, humanPax3 protein, mousePAX3 Transcription Factor

Identifiers

PMID37968277
PMCPMC10651858
OpenAlexW4388705446

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.