Evidence map›Paper›PMID 24107773›Full record

ArticleEpigenetics2013

Fundamental differences in promoter CpG island DNA hypermethylation between human cancer and genetically engineered mouse models of cancer.

Scott J Diede, Zizhen Yao, C Chip Keyes, Ashlee E Tyler, Joyoti Dey, Christopher S Hackett, Katrina Elsaesser, Christopher J Kemp, Paul E Neiman, William A Weiss and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Epigenetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Dynamic epigenetic regulation of glioblastoma tumorigenicity through LSD1 modulation of MYC expression.Proceedings of the National Academy of Sciences of the United States of America · 2015
    Article
  13. Article
  14. Article
  15. Chemotherapy and chemoprevention by thiazolidinediones.BioMed research international · 2015
    Review
  16. Article
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.

Scott J DiedeDivision of Clinical Research; Fred Hutchinson Cancer Research Center; Seattle, WA USA; Department of Pediatrics; University of Washington School of Medicine; Seattle, WA USA.
Zizhen YaoDivision of Human Biology; Fred Hutchinson Cancer Research Center; Seattle, WA USA.
C Chip KeyesDivision of Human Biology; Fred Hutchinson Cancer Research Center; Seattle, WA USA.
Ashlee E TylerDivision of Human Biology; Fred Hutchinson Cancer Research Center; Seattle, WA USA.
Joyoti DeyDivision of Clinical Research; Fred Hutchinson Cancer Research Center; Seattle, WA USA.
Christopher S HackettDepartment of Neurological Surgery; University of California at San Francisco; San Francisco, CA USA; Department of Neurology; University of California at San Francisco; San Francisco, CA USA; Department of Pediatrics; University of California at San Francisco; San Francisco, CA USA.
Katrina ElsaesserDivision of Basic Sciences; Fred Hutchinson Cancer Research Center; Seattle, WA USA.
Christopher J KempDivision of Basic Sciences; Fred Hutchinson Cancer Research Center; Seattle, WA USA; Division of Public Health Sciences; Fred Hutchinson Cancer Research Center; Seattle, WA USA.
Paul E NeimanDivision of Basic Sciences; Fred Hutchinson Cancer Research Center; Seattle, WA USA; Department of Medicine; University of Washington School of Medicine; Seattle, WA USA.
William A WeissDepartment of Neurological Surgery; University of California at San Francisco; San Francisco, CA USA; Department of Neurology; University of California at San Francisco; San Francisco, CA USA; Department of Pediatrics; University of California at San Francisco; San Francisco, CA USA.
James M OlsonDivision of Clinical Research; Fred Hutchinson Cancer Research Center; Seattle, WA USA; Department of Pediatrics; University of Washington School of Medicine; Seattle, WA USA.
Stephen J TapscottDivision of Clinical Research; Fred Hutchinson Cancer Research Center; Seattle, WA USA; Division of Human Biology; Fred Hutchinson Cancer Research Center; Seattle, WA USA; Department of Neurology; University of Washington School of Medicine; Seattle, WA USA.
Fred Hutch Cancer Center · USClinical Research Management · USUniversity of California, San Francisco · USCape Town HVTN Immunology Laboratory / Hutchinson Centre Research Institute of South Africa · ZAOffice of Basic Energy Sciences · USSeattle University · USUniversity of Washington · US

Funding

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
Testing a cancer patient-specific SARS-CoV-2 vaccine in chemotherapy- and radiation-treated pediatric brain tumor mouse modelsR01CA114567 · NCI · SEATTLE CHILDREN'S HOSPITAL · PI OLSON, JAMES M · 2006 to 2023
$4.9M
Cellular and Molecular Biology of Childhood DiseaseK12HD043376 · NICHD · UNIVERSITY OF WASHINGTON · PI STAPLETON, FIELDING BRUDER · 2003 to 2012
$3.3M
Infant and Toddler Brain TumorsR01CA155360 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI OLSON, JAMES M · 2011 to 2015
$1.8M
NCI NIH HHS R01 CA114567NCI NIH HHS R01 CA155360NIAMS NIH HHS AR045113NIAMS NIH HHS R01 AR045113NICHD NIH HHS K12 HD043376NICHD NIH HHS K12 HD43376NICHD NIH HHS T32 HD007183
6 · The paper itself

Abstract

Genetic and epigenetic alterations are essential for the initiation and progression of human cancer. We previously reported that primary human medulloblastomas showed extensive cancer-specific CpG island DNA hypermethylation in critical developmental pathways. To determine whether genetically engineered mouse models (GEMMs) of medulloblastoma have comparable epigenetic changes, we assessed genome-wide DNA methylation in three mouse models of medulloblastoma. In contrast to human samples, very few loci with cancer-specific DNA hypermethylation were detected, and in almost all cases the degree of methylation was relatively modest compared with the dense hypermethylation in the human cancers. To determine if this finding was common to other GEMMs, we examined a Burkitt lymphoma and breast cancer model and did not detect promoter CpG island DNA hypermethylation, suggesting that human cancers and at least some GEMMs are fundamentally different with respect to this epigenetic modification. These findings provide an opportunity to both better understand the mechanism of aberrant DNA methylation in human cancer and construct better GEMMs to serve as preclinical platforms for therapy development.

Indexed as

CpG IslandsPromoter Regions, GeneticAnimalsBreast NeoplasmsBurkitt LymphomaCerebellar NeoplasmsDNA MethylationFemaleHumansMedulloblastomaMiceMice, TransgenicNeoplasmsNeoplasms, ExperimentalcancerDNA methylationepigenomicsgenetically engineered mouse modelsmedulloblastoma

Identifiers

PMID24107773
PMCPMC3933486
OpenAlexW2032312933

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.