Evidence map›Paper›PMID 24092238›Full record

ArticleCancer research2013

MyoD is a tumor suppressor gene in medulloblastoma.

Joyoti Dey, Adrian M Dubuc, Kyle D Pedro, Derek Thirstrup, Brig Mecham, Paul A Northcott, Xiaochong Wu, David Shih, Stephen J Tapscott, Michael LeBlanc and 2 more

Open access · greenAbstract read
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

19 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Genetic and molecular alterations across medulloblastoma subgroups.Journal of molecular medicine (Berlin, Germany) · 2015
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
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

12 authors at 7 institutions in 3 countries.

Joyoti DeyAuthors' Affiliations: Molecular and Cellular Biology Program, University of Washington; Clinical Research Division, Human Biology Division, and Public Health Sciences Division, Fred Hutchinson Cancer Research Center; Presage Biosciences; Sage Bionetworks; Seattle Children's Hospital, Seattle, Washington; Arthur and Sonia Labatt Brain Tumor Research Center and Division of Neurosurgery, The Hospital for Sick Children, Toronto, Ontario, Canada.
Adrian M Dubuc
Kyle D Pedro
Derek Thirstrup
Brig Mecham
Paul A Northcott
Xiaochong Wu
David Shih
Stephen J Tapscott
Michael LeBlanc
Michael D Taylor
James M Olson
Cancer Research Center · USHospital for Sick Children · CAPresage Biosciences (United States) · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZASage Bionetworks · USSickKids Foundation · CAUniversity of Washington · US

Funding

Integrating cancer datasets for predictive model development and trainingU54CA149237 · NCI · SAGE BIONETWORKS · PI FRIEND, STEPHEN HENRY · 2010 to 2014
$8.9M
LINEAGE DETERMINATION IN MUSCLER01AR045113 · NIAMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI TAPSCOTT, STEPHEN J · 1998 to 2017
$6.8M
INTERDISCIPLINARY TRAINING IN DEVELOPMENTAL BIOLOGYT32HD007183 · NICHD · UNIVERSITY OF WASHINGTON · PI RAIBLE, DAVID W · 1985 to 2015
$5.7M
Infant and Toddler Brain TumorsR01CA155360 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI OLSON, JAMES M · 2011 to 2015
$1.8M
bHLH Factors in Medulloblastoma Genesis and MaintenanceR01CA112350 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI OLSON, JAMES M · 2005 to 2008
$1.3M
CIHRNCI NIH HHS 5R01CA112350NCI NIH HHS 5R01CA11456705NCI NIH HHS R01 CA112350NCI NIH HHS R01 CA155360NCI NIH HHS U54 CA149237NCI NIH HHS U54CA149237NIAMS NIH HHS R01 AR045113NIAMS NIH HHS R01AR045113NICHD NIH HHS 5T32HD007183NICHD NIH HHS T32 HD007183
6 · The paper itself

Abstract

While medulloblastoma, a pediatric tumor of the cerebellum, is characterized by aberrations in developmental pathways, the majority of genetic determinants remain unknown. An unbiased Sleeping Beauty transposon screen revealed MyoD as a putative medulloblastoma tumor suppressor. This was unexpected, as MyoD is a muscle differentiation factor and not previously known to be expressed in cerebellum or medulloblastoma. In response to deletion of one allele of MyoD, two other Sonic hedgehog-driven mouse medulloblastoma models showed accelerated tumor formation and death, confirming MyoD as a tumor suppressor in these models. In normal cerebellum, MyoD was expressed in the proliferating granule neuron progenitors that are thought to be precursors to medulloblastoma. Similar to some other tumor suppressors that are induced in cancer, MyoD was expressed in proliferating medulloblastoma cells in three mouse models and in human medulloblastoma cases. This suggests that although expression of MyoD in a proliferating tumor is insufficient to prevent tumor progression, its expression in the cerebellum hinders medulloblastoma genesis.

Indexed as

AnimalsCell ProliferationCell Transformation, NeoplasticCerebellar NeoplasmsCerebellumDisease ProgressionGene DeletionGene Expression Regulation, NeoplasticGenes, Tumor SuppressorHumansMedulloblastomaMiceMice, TransgenicMyoD ProteinMyoD1 myogenic differentiation proteinMyoD Protein

Identifiers

PMID24092238
PMCPMC4014678
OpenAlexW2114308127

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.