Evidence map›Paper›PMID 23251566›Full record

ArticlePloS one2012

High DNA methyltransferase DNMT3B levels: a poor prognostic marker in acute myeloid leukemia.

Sandrine Hayette, Xavier Thomas, Laurent Jallades, Kaddour Chabane, Carole Charlot, Isabelle Tigaud, Sophie Gazzo, Stéphane Morisset, Pascale Cornillet-Lefebvre, Adriana Plesa and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 67 citations in OpenAlex.

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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

16 authors at 5 institutions in 1 country.

Sandrine HayetteService d'Hématologie Biologique, Centre Hospitalier Lyon-Sud, Pierre-Bénite France, Hospices Civils de Lyon, Lyon, France. sandrine.hayette@chu-lyon.fr
Xavier Thomas
Laurent Jallades
Kaddour Chabane
Carole Charlot
Isabelle Tigaud
Sophie Gazzo
Stéphane Morisset
Pascale Cornillet-Lefebvre
Adriana Plesa
Sarah Huet
Aline Renneville
Gilles Salles
Franck Emmanuel Nicolini
Jean-Pierre Magaud
Mauricette Michallet
Hospices Civils de Lyon · FRHôpital Lyon Sud · FRUniversité Claude Bernard Lyon 1 · FRCentre Hospitalier Universitaire de Lille · FRUniversité de Reims Champagne-Ardenne · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It has been recently shown that DNA methyl transferase overexpression is correlated with unfavourable prognosis in human malignancies while methylation deregulation remains a hallmark that defines acute myeloid leukemia (AML). The oncogenic transcription factor EVI1 is involved in methylation deregulation and its overexpression plays a major role for predicting an adverse outcome. Moreover, the identification of DNMT3A mutations in AML patients has recently been described as a poor prognostic indicator. In order to clarify relationship between these key actors in methylation mechanisms and their potential impact on patient outcomes, we analysed 195 de novo AML patients for the expression of DNMT3A, 3B (and its non-catalytic variant 3B(NC)) and their correlations with the outcome and the expression of other common prognostic genetic biomarkers (EVI1, NPM1, FLT3ITD/TKD and MLL) in adult AML. The overexpression of DNMT3B/3B(NC) is (i) significantly correlated with a shorter overall survival, and (ii) inversely significantly correlated with event-free survival and DNMT3A expression level. Moreover, multivariate analysis showed that a high expression level of DNMT3B/3B(NC) is statistically a significant independent poor prognostic indicator. This study represents the first report showing that the overexpression of DNMT3B/3B(NC) is an independent predictor of poor survival in AML. Its quantification should be implemented to the genetic profile used to stratify patients for therapeutical strategies and should be useful to identify patients who may benefit from therapy based on demethylating agents.

Indexed as

AdolescentAdultAgedAmino Acid SequenceBiomarkers, TumorDisease-Free SurvivalDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNA Methyltransferase 3BDNA Mutational AnalysisExonsFemaleHumansLeukemia, Myeloid, AcuteMaleMiddle AgedBiomarkers, TumorDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3ADNA Methyltransferase 3BDNMT3A protein, humanNeoplasm ProteinsNPM1 protein, humanNucleophosmin

Identifiers

PMID23251566
PMCPMC3519733
OpenAlexW1978788671

What OpenQuestion holds

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LicenceCC BY
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.