Evidence map›Paper›PMID 31533980›Full record

ArticleGenome research2019

Transcriptional alterations in glioma result primarily from DNA methylation-independent mechanisms.

Franck Court, Elisa Le Boiteux, Anne Fogli, Mélanie Müller-Barthélémy, Catherine Vaurs-Barrière, Emmanuel Chautard, Bruno Pereira, Julian Biau, Jean-Louis Kemeny, Toufic Khalil and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
–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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Article
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  11. NAR cancer · 2023
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  18. The Long Non-Coding RNAInternational journal of molecular sciences · 2022
    Article
  19. Article
  20. Expression and potential role of FOSB in glioma.Frontiers in molecular neuroscience · 2022
    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

13 authors at 5 institutions in 1 country.

Franck CourtLaboratoire Génétique Reproduction et Développement (GReD), Université Clermont Auvergne, CNRS, INSERM, BP 38, Clermont-Ferrand 63001, France.
Elisa Le BoiteuxLaboratoire Génétique Reproduction et Développement (GReD), Université Clermont Auvergne, CNRS, INSERM, BP 38, Clermont-Ferrand 63001, France.
Anne FogliLaboratoire Génétique Reproduction et Développement (GReD), Université Clermont Auvergne, CNRS, INSERM, BP 38, Clermont-Ferrand 63001, France.
Mélanie Müller-BarthélémyLaboratoire Génétique Reproduction et Développement (GReD), Université Clermont Auvergne, CNRS, INSERM, BP 38, Clermont-Ferrand 63001, France.
Catherine Vaurs-BarrièreLaboratoire Génétique Reproduction et Développement (GReD), Université Clermont Auvergne, CNRS, INSERM, BP 38, Clermont-Ferrand 63001, France.
Emmanuel ChautardPathology Department, Jean Perrin Center, Clermont-Ferrand 63011, France.
Bruno PereiraBiostatistics Department, Délégation à la Recherche Clinique et à l'Innovation, Clermont-Ferrand Hospital, Clermont-Ferrand 63003, France.
Julian BiauUniversité Clermont Auvergne, INSERM, U1240 IMoST, Clermont-Ferrand 63011, France.
Jean-Louis KemenyPathology Department, Université Clermont Auvergne and Clermont-Ferrand Hospital, Clermont-Ferrand 63003, France.
Toufic KhalilDepartment of Neurosurgery, Clermont-Ferrand Hospital, Clermont-Ferrand 63003, France.
Lucie Karayan-TaponINSERM, U1084, Poitiers 86021, France.
Pierre VerrelleINSERM, U1196 CNRS UMR9187, Curie Institute, Orsay 91405, France.
Philippe ArnaudLaboratoire Génétique Reproduction et Développement (GReD), Université Clermont Auvergne, CNRS, INSERM, BP 38, Clermont-Ferrand 63001, France.ORCID 0000-0002-7937-8764
Centre National de la Recherche Scientifique · FRInserm · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRInstitut Génétique, Reproduction et Développement · FRUniversité Clermont Auvergne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In cancer cells, aberrant DNA methylation is commonly associated with transcriptional alterations, including silencing of tumor suppressor genes. However, multiple epigenetic mechanisms, including polycomb repressive marks, contribute to gene deregulation in cancer. To dissect the relative contribution of DNA methylation-dependent and -independent mechanisms to transcriptional alterations at CpG island/promoter-associated genes in cancer, we studied 70 samples of adult glioma, a widespread type of brain tumor, classified according to their isocitrate dehydrogenase (

Indexed as

Transcription, GeneticAdultCell Line, TumorChromatinCpG IslandsDNA MethylationEpigenesis, GeneticFemaleGene Expression Regulation, NeoplasticGliomaHistonesHumansIsocitrate DehydrogenaseJumonji Domain-Containing Histone DemethylasesMalePromoter Regions, GeneticChromatinHistonesIDH1 protein, humanIsocitrate DehydrogenaseJumonji Domain-Containing Histone Demethylases

Identifiers

PMID31533980
PMCPMC6771409
OpenAlexW2974702474

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.