Evidence map›Paper›PMID 19966297›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2010

DNA methylation of developmental genes in pediatric medulloblastomas identified by denaturation analysis of methylation differences.

Scott J Diede, Jamie Guenthoer, Linda N Geng, Sarah E Mahoney, Michael Marotta, James M Olson, Hisashi Tanaka, Stephen J Tapscott

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 63 citations in OpenAlex.

  1. Extracellular ssDNA fromInternational journal of molecular sciences · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Epigenetic regulation in medulloblastoma.Molecular and cellular neurosciences · 2018
    Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 1 country.

Scott J DiedeDivision of Clinical Research, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, USA.
Jamie Guenthoer
Linda N Geng
Sarah E Mahoney
Michael Marotta
James M Olson
Hisashi Tanaka
Stephen J Tapscott
Fred Hutch Cancer Center · USCleveland Clinic · USCleveland Clinic Lerner College of Medicine · USClinical Research Management · US

Funding

MYOTONIC DYSTROPHY LOCUS CONTROLR01AR045203 · NIAMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI TAPSCOTT, STEPHEN J · 1998 to 2025
$9.4M
PEDIATRIC ONCOLOGY RESEARCH TRAINING PROGRAMT32CA009351 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI Elizabeth R Lawlor, SOHEIL MESHINCHI · 1985 to 2026
$7.0M
LINEAGE DETERMINATION IN MUSCLER01AR045113 · NIAMS · FRED HUTCHINSON CANCER RESEARCH CENTER · PI TAPSCOTT, STEPHEN J · 1998 to 2017
$6.8M
Cellular and Molecular Biology of Childhood DiseaseK12HD043376 · NICHD · UNIVERSITY OF WASHINGTON · PI STAPLETON, FIELDING BRUDER · 2003 to 2012
$3.3M
NCI NIH HHS 2T32CA009351NCI NIH HHS T32 CA009351NIAMS NIH HHS AR045113NIAMS NIH HHS AR045203NIAMS NIH HHS R01 AR045113NIAMS NIH HHS R01 AR045203NICHD NIH HHS K12 HD043376NICHD NIH HHS K12 HD43376
6 · The paper itself

Abstract

DNA methylation might have a significant role in preventing normal differentiation in pediatric cancers. We used a genomewide method for detecting regions of CpG methylation on the basis of the increased melting temperature of methylated DNA, termed denaturation analysis of methylation differences (DAMD). Using the DAMD assay, we find common regions of cancer-specific methylation changes in primary medulloblastomas in critical developmental regulatory pathways, including Sonic hedgehog (Shh), Wingless (Wnt), retinoic acid receptor (RAR), and bone morphogenetic protein (BMP). One of the commonly methylated loci is the PTCH1-1C promoter, a negative regulator of the Shh pathway that is methylated in both primary patient samples and human medulloblastoma cell lines. Treatment with the DNA methyltransferase inhibitor 5-aza-2'-deoxycytidine (5-aza-dC) increases the expression of PTCH1 and other methylated loci. Whereas genetic mutations in PTCH1 have previously been shown to lead to medulloblastoma, our study indicates that epigenetic silencing of PTCH1, and other critical developmental loci, by DNA methylation is a fundamental process of pediatric medulloblastoma formation. This finding warrants strong consideration for DNA demethylating agents in future clinical trials for children with this disease.

Indexed as

DNA MethylationGenes, DevelopmentalCell Line, TumorChildCpG IslandsEpigenesis, GeneticGene SilencingHumansMedulloblastomaMicroarray AnalysisPatched-1 ReceptorPatched ReceptorsPromoter Regions, GeneticReceptors, Cell SurfacePatched-1 ReceptorPatched ReceptorsPTCH1 protein, humanReceptors, Cell Surface

Identifiers

PMID19966297
PMCPMC2806770
OpenAlexW2131221461

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.