Evidence map›Paper›PMID 24852755›Full record

ArticlePloS one2014

3-Deazaneplanocin A (DZNep), an inhibitor of the histone methyltransferase EZH2, induces apoptosis and reduces cell migration in chondrosarcoma cells.

Nicolas Girard, Céline Bazille, Eva Lhuissier, Hervé Benateau, Antonio Llombart-Bosch, Karim Boumediene, Catherine Bauge

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

46 citing papers in PubMed, 83 citations in OpenAlex.

  1. Review
  2. Article
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  4. Exploring adenosine analogs for chondrosarcoma therapy:Molecular therapy. Nucleic acids · 2025
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  6. Review
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  9. Epigenetic Abnormalities in Chondrosarcoma.International journal of molecular sciences · 2023
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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

7 authors at 2 institutions in 2 countries.

Nicolas GirardNormandie Univ, Caen, France; UNICAEN, EA4652 MILPAT, Caen, France.
Céline BazilleNormandie Univ, Caen, France; UNICAEN, EA4652 MILPAT, Caen, France; Service d'Anatomie Pathologique, CHU, Caen, France.
Eva LhuissierNormandie Univ, Caen, France; UNICAEN, EA4652 MILPAT, Caen, France.
Hervé BenateauNormandie Univ, Caen, France; UNICAEN, EA4652 MILPAT, Caen, France; Service de Chirurgie Maxillo-faciale, CHU, Caen, France.
Antonio Llombart-BoschPathology Department, University of Valencia, Valencia, Spain.
Karim BoumedieneNormandie Univ, Caen, France; UNICAEN, EA4652 MILPAT, Caen, France.
Catherine BaugeNormandie Univ, Caen, France; UNICAEN, EA4652 MILPAT, Caen, France.
Normandie Université · FRUniversitat de València · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveGrowing evidences indicate that the histone methyltransferase EZH2 (enhancer of zeste homolog 2) may be an appropriate therapeutic target in some tumors. Indeed, a high expression of EZH2 is correlated with poor prognosis and metastasis in many cancers. In addition, 3-Deazaneplanocin A (DZNep), an S-adenosyl-L homocysteine hydrolase inhibitor which induces EZH2 protein depletion, leads to cell death in several cancers and tumors. The aim of this study was to determine whether an epigenetic therapy targeting EZH2 with DZNep may be also efficient to treat chondrosarcomas.

methodsEZH2 expression was determined by immunohistochemistry and western-blot. Chondrosarcoma cell line CH2879 was cultured in the presence of DZNep, and its growth and survival were evaluated by counting adherent cells periodically. Apoptosis was assayed by cell cycle analysis, Apo2.7 expression using flow cytometry, and by PARP cleavage using western-blot. Cell migration was assessed by wound healing assay.

resultsChondrosarcomas (at least with high grade) highly express EZH2, at contrary to enchondromas or chondrocytes. In vitro, DZNep inhibits EZH2 protein expression, and subsequently reduces the trimethylation of lysine 27 on histone H3 (H3K27me3). Interestingly, DZNep induces cell death of chondrosarcoma cell lines by apoptosis, while it slightly reduces growth of normal chondrocytes. In addition, DZNep reduces cell migration.

conclusionThese results indicate that an epigenetic therapy that pharmacologically targets EZH2 via DZNep may constitute a novel approach to treat chondrosarcomas.

Indexed as

AdenosineApoptosisCell Line, TumorCell MovementChondrosarcomaEnzyme InhibitorsFlow CytometryHistone-Lysine N-MethyltransferaseHistone MethyltransferasesHumansReverse Transcriptase Polymerase Chain Reaction3-deazaneplanocinAdenosineEnzyme InhibitorsHistone-Lysine N-MethyltransferaseHistone Methyltransferases

Identifiers

PMID24852755
PMCPMC4031152
OpenAlexW1983545974

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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.