Evidence map›Paper›PMID 23533570›Full record

ArticlePloS one2013

Chordoma characterization of significant changes of the DNA methylation pattern.

Beate Rinner, Andreas Weinhaeusel, Birgit Lohberger, Elke Verena Froehlich, Walter Pulverer, Carina Fischer, Katharina Meditz, Susanne Scheipl, Slave Trajanoski, Christian Guelly and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

17 citing papers in PubMed, 48 citations in OpenAlex.

  1. Review
  2. Chordoma cells possess bone-dissolving activity at the bone invasion front.Cellular oncology (Dordrecht, Netherlands) · 2024
    Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. The molecular aspects of chordoma.Neurosurgical review · 2016
    Review
  13. Epigenetic deregulations in chordoma.Cell proliferation · 2015
    Review
  14. Article
  15. Article
  16. Article
  17. Carcinogenesis of PIK3CA.Hereditary cancer in clinical practice · 2013
    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 3 institutions in 1 country.

Beate RinnerCenter for Medical Research, Medical University Graz, Graz, Austria. beate.rinner@medunigraz.at
Andreas Weinhaeusel
Birgit Lohberger
Elke Verena Froehlich
Walter Pulverer
Carina Fischer
Katharina Meditz
Susanne Scheipl
Slave Trajanoski
Christian Guelly
Andreas Leithner
Bernadette Liegl
Medical University of Graz · ATAustrian Institute of Technology · ATUniversity of Graz · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chordomas are rare mesenchymal tumors occurring exclusively in the midline from clivus to sacrum. Early tumor detection is extremely important as these tumors are resistant to chemotherapy and irradiation. Despite continuous research efforts surgical excision remains the main treatment option. Because of the often challenging anatomic location early detection is important to enable complete tumor resection and to reduce the high incidence of local recurrences. The aim of this study was to explore whether DNA methylation, a well known epigenetic marker, may play a role in chordoma development and if hypermethylation of specific CpG islands may serve as potential biomarkers correlated with SNP analyses in chordoma. The study was performed on tumor samples from ten chordoma patients. We found significant genomic instability by Affymetrix 6.0. It was interesting to see that all chordomas showed a loss of 3q26.32 (PIK 3CA) and 3q27.3 (BCL6) thus underlining the potential importance of the PI3K pathway in chordoma development. By using the AITCpG360 methylation assay we elucidated 20 genes which were hyper/hypomethylated compared to normal blood. The most promising candidates were nine hyper/hypomethylated genes C3, XIST, TACSTD2, FMR1, HIC1, RARB, DLEC1, KL, and RASSF1. In summary, we have shown that chordomas are characterized by a significant genomic instability and furthermore we demonstrated a characteristic DNA methylation pattern. These findings add new insights into chordoma development, diagnosis and potential new treatment options.

Indexed as

AdultAgedAntigens, NeoplasmCell Adhesion MoleculesChordomaDNA MethylationFemaleFragile X Messenger Ribonucleoprotein 1HumansKruppel-Like Transcription FactorsMaleMiddle AgedOligonucleotide Array Sequence AnalysisReceptors, Retinoic AcidRNA, Long NoncodingTumor Suppressor ProteinsAntigens, NeoplasmCell Adhesion MoleculesDLEC1 protein, humanFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1HIC1 protein, humanKruppel-Like Transcription FactorsRASSF1 protein, humanReceptors, Retinoic Acidretinoic acid receptor betaRNA, Long NoncodingTACSTD2 protein, humanTumor Suppressor ProteinsXIST non-coding RNA

Identifiers

PMID23533570
PMCPMC3606365
OpenAlexW2045620441

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.