Evidence map›Paper›PMID 35483358›Full record

ArticleDevelopmental cell2022

The myogenesis program drives clonal selection and drug resistance in rhabdomyosarcoma.

Anand G Patel, Xiang Chen, Xin Huang, Michael R Clay, Natalia Komorova, Matthew J Krasin, Alberto Pappo, Heather Tillman, Brent A Orr, Justina McEvoy and 10 more

Abstract read
In one paragraph

Article in Developmental cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
–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

54 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  17. PLA2 driven lipid signaling drives ARMS tumorigenic cell properties.Cell communication and signaling : CCS · 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

20 authors.

Anand G PatelDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA; Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Xiang ChenDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Xin HuangDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Michael R ClayDepartment of Pathology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Natalia KomorovaDepartment of Mathematics, University of California, Irvine, CA 92697, USA.
Matthew J KrasinDepartment of Radiation Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Alberto PappoDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Heather TillmanDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Brent A OrrDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Justina McEvoyDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Brittney GordonDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Kaley BlankenshipDepartment of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Colleen ReillyDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Xin ZhouDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Jackie L NorrieDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Asa KarlstromDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Jiyang YuDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Dominik WodarzDepartment of Population Health and Disease Prevention, Program in Public Health, Susan and Henry Samueli College of Health Sciences, University of California, Irvine, CA 92697, USA.
Elizabeth StewartDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA; Department of Oncology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA.
Michael A DyerDepartment of Developmental Neurobiology, St. Jude Children's Research Hospital, Memphis, TN 38105, USA. Electronic address: michael.dyer@stjude.org.

Funding

Viral Vector Technology (VVTSR)P30CA021765 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI CHARLES ROBERTS · 1985 to 2026
$166.9M
In Vivo Testing of Novel Drug Combinations for Pediatric Soft Tissue SarcomasU01CA263969 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Michael A Dyer, Elizabeth A Stewart · 2021 to 2026
$4.0M
The Role of Immature Tumor Subpopulations In Pediatric RhabdomyosarcomaR01CA262790 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI Xiang Chen · 2022 to 2026
$2.1M
Novel Therapeutic Approaches for the Treatment of RhabdomyosarcomaR01CA219686 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI DYER, MICHAEL A · 2017 to 2021
$2.0M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA021765NCI NIH HHS R01 CA219686NCI NIH HHS R01 CA262790NCI NIH HHS U01 CA263969
6 · The paper itself

Abstract

Rhabdomyosarcoma (RMS) is a pediatric cancer with features of skeletal muscle; patients with unresectable or metastatic RMS fare poorly due to high rates of disease recurrence. Here, we use single-cell and single-nucleus RNA sequencing to show that RMS tumors recapitulate the spectrum of embryonal myogenesis. Using matched patient samples from a clinical trial and orthotopic patient-derived xenografts (O-PDXs), we show that chemotherapy eliminates the most proliferative component with features of myoblasts within embryonal RMS; after treatment, the immature population with features of paraxial mesoderm expands to reconstitute the developmental hierarchy of the original tumor. We discovered that this paraxial mesoderm population is dependent on EGFR signaling and is sensitive to EGFR inhibitors. Taken together, these data serve as a proof of concept that targeting each developmental state in embryonal RMS is an effective strategy for improving outcomes by preventing disease recurrence.

Indexed as

RhabdomyosarcomaRhabdomyosarcoma, EmbryonalChildDrug ResistanceErbB ReceptorsHumansMuscle DevelopmentNeoplasm Recurrence, LocalErbB Receptorscancer recurrencemuscle developmentsarcomasingle-cell biologytumor heterogeneity

Identifiers

PMID35483358
PMCPMC9133224

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.