Evidence map›Paper›PMID 16416310›Full record

ReviewJournal of molecular medicine (Berlin, Germany)2006

Quantitative assessment of DNA methylation: Potential applications for disease diagnosis, classification, and prognosis in clinical settings.

Romulo Martin Brena, Tim Hui-Ming Huang, Christoph Plass

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of molecular medicine (Berlin, Germany), 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Genome-wide epigenetic modifications in cancer.Progress in drug research. Fortschritte der Arzneimittelforschung. Progres des recherches pharmaceutiques · 2011
    Review
  13. Article
  14. Identification of epigenetic DNA modifications with a protein nanopore.Chemical communications (Cambridge, England) · 2010
    Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

3 authors.

Romulo Martin BrenaDivision of Human Cancer Genetics, Department of Molecular Genetics, The Ohio State University, Columbus, OH 43210, USA.
Tim Hui-Ming Huang
Christoph Plass

Funding

GENOMIC SCANNING IN ORAL CANCERR01DE013123 · NIDCR · OHIO STATE UNIVERSITY · PI PLASS, CHRISTOPH · 2000 to 2011
$2.3M
DNA methylation as a diagnostic marker in AMLR01CA093548 · NCI · OHIO STATE UNIVERSITY · PI PLASS, CHRISTOPH · 2002 to 2006
$1.5M
NCI NIH HHS CA93548NIDCR NIH HHS DE13123
6 · The paper itself

Abstract

Deregulation of the epigenome is now recognized as a major mechanism involved in the development and progression of human diseases such as cancer. As opposed to the irreversible nature of genetic events, which introduce changes in the primary DNA sequence, epigenetic modifications are reversible and leave the original DNA sequence intact. There is now evidence that the epigenetic landscape in humans undergoes modifications as the result of normal aging, with older individuals exhibiting higher levels of promoter hypermethylation compared to younger ones. Thus, it has been proposed that the higher incidence of certain disease in older individuals might be, in part, a consequence of an inherent change in the control and regulation of the epigenome. These observations are of remarkable clinical significance since the aberrant epigenetic changes characteristic of disease provide a unique platform for the development of new therapeutic approaches. In this review, we address the significance of DNA methylation changes that result or lead to disease, occur with aging, or may be the result of environmental exposure. We provide a detailed description of quantitative techniques currently available for the detection and analysis of DNA methylation and provide a comprehensive framework that may allow for the incorporation of protocols which include DNA methylation as a tool for disease diagnosis and classification, which could lead to the tailoring of therapeutic approaches designed to individual patient needs.

Indexed as

DNA MethylationGenetic TechniquesChromatography, High Pressure LiquidEnvironmentEpigenesis, GeneticGene Expression Regulation, DevelopmentalGenetic MarkersGenome, HumanHumansNeoplasmsOligonucleotide Array Sequence AnalysisPolymerase Chain ReactionPrognosisReference ValuesSequence Analysis, DNASpectrometry, Mass, Matrix-Assisted Laser Desorption-IonizationGenetic Markershydrogen sulfiteSulfites

Identifiers

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.