Evidence map›Paper›PMID 36127469›Full record

ArticleCommunications biology2022

Haploinsufficiency of the lysosomal sialidase NEU1 results in a model of pleomorphic rhabdomyosarcoma in mice.

Eda R Machado, Diantha van de Vlekkert, Heather S Sheppard, Scott Perry, Susanna M Downing, Jonathan Laxton, Richard Ashmun, David B Finkelstein, Geoffrey A Neale, Huimin Hu and 4 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.5field-weighted citation impact, top 39% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Autophagy · 2026
    Article
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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

14 authors at 1 institution in 1 country.

Eda R Machado *Department of Genetics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Diantha van de Vlekkert *Department of Genetics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0001-7498-1292
Heather S Sheppard *Department of Pathology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0002-9623-2812
Scott Perry *Flow Cytometry Core Facility, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Susanna M DowningDepartment of Cell & Molecular Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Jonathan LaxtonFlow Cytometry Core Facility, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Richard AshmunFlow Cytometry Core Facility, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
David B FinkelsteinDepartment of Computational Biology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Geoffrey A NealeHartwell Center for Bioinformatics and Biotechnology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0003-3776-0858
Huimin HuDepartment of Genetics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Frank C HarwoodDepartment of Genetics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.
Selene C KooDepartment of Pathology, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA.ORCID 0000-0001-8459-2469
Gerard C GrosveldDepartment of Genetics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA. gerard.grosveld@stjude.org.ORCID 0000-0002-6583-1265
Alessandra d'AzzoDepartment of Genetics, St. Jude Children's Research Hospital, Memphis, TN, 38105, USA. sandra.dazzo@stjude.org.ORCID 0000-0003-1747-7502
St. Jude Children's Research Hospital · US

Funding

Excessive Lysosomal Exocytosis Triggers Pathogenic Mechanisms in Sialidosis MiceR01GM104981 · NIGMS · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI D'AZZO, ALESSANDRA · 2013 to 2017
$1.4M
NIGMS NIH HHS R01 GM104981
6 · The paper itself

Abstract

Rhabdomyosarcoma, the most common pediatric sarcoma, has no effective treatment for the pleomorphic subtype. Still, what triggers transformation into this aggressive phenotype remains poorly understood. Here we used Ptch1

Indexed as

NeuraminidaseRhabdomyosarcomaAnimalsHaploinsufficiencyHumansLysosomal-Associated Membrane Protein 1LysosomesMiceTumor MicroenvironmentLysosomal-Associated Membrane Protein 1Neu1 protein, mouseNeuraminidase

Identifiers

PMID36127469
PMCPMC9489700
OpenAlexW4296426082

What OpenQuestion holds

Textmetadata
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.