Evidence map›Paper›PMID 20186319›Full record

ArticlePloS one2010

Influence of genetic background and tissue types on global DNA methylation patterns.

Howard H Yang, Nan Hu, Chaoyu Wang, Ti Ding, Barbara K Dunn, Alisa M Goldstein, Philip R Taylor, Maxwell P Lee

Abstract read
In one paragraph

Article in PloS one, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–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

22 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Epigenetics of Trauma Transmission and Fetal Alcohol Spectrum Disorder: What Does the Evidence Support?International journal of environmental research and public health · 2023
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. DNA methylation: an epigenetic risk factor in preterm birth.Reproductive sciences (Thousand Oaks, Calif.) · 2012
    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

8 authors.

Howard H YangLaboratory of Population Genetics, Center for Cancer Research, National Cancer Institute, Bethesda, Maryland, United States of America.
Nan Hu
Chaoyu Wang
Ti Ding
Barbara K Dunn
Alisa M Goldstein
Philip R Taylor
Maxwell P Lee

Funding

Genetics and Epigenetics of CancerZIABC011253 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LEE, MAXWELL · 2010 to 2012
$2.4M
Allele-specific gene expression and epigenetic informationZIABC010986 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LEE, MAXWELL · 2009 to 2012
$2.2M
Informatics Solutions to Biomedical ResearchZIABC011250 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI LEE, MAXWELL · 2010 to 2012
$236k
Intramural NIH HHS
6 · The paper itself

Abstract

Recent studies have shown a genetic influence on gene expression variation, chromatin, and DNA methylation. However, the effects of genetic background and tissue types on DNA methylation at the genome-wide level have not been characterized extensively. To study the effect of genetic background and tissue types on global DNA methylation, we performed DNA methylation analysis using the Affymetrix 500K SNP array on tumor, adjacent normal tissue, and blood DNA from 30 patients with esophageal squamous cell carcinoma (ESCC). The use of multiple tissues from 30 individuals allowed us to evaluate variation of DNA methylation states across tissues and individuals. Our results demonstrate that blood and esophageal tissues shared similar DNA methylation patterns within the same individual, suggesting an influence of genetic background on DNA methylation. Furthermore, we showed that tissue types are important contributors of DNA methylation states.

Indexed as

DNA MethylationCarcinoma, Squamous CellDNA, NeoplasmEsophageal NeoplasmsEsophagusGene Expression ProfilingGenotypeHumansOligonucleotide Array Sequence AnalysisPolymorphism, Single NucleotidePrincipal Component AnalysisDNA, Neoplasm

Identifiers

PMID20186319
PMCPMC2826396

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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.