Evidence map›Paper›PMID 25437053›Full record

ArticleEpigenetics2014

Global histone deacetylase enzymatic activity is an independent prognostic marker associated with a shorter overall survival in chronic lymphocytic leukemia patients.

Michaël Van Damme, Emerence Crompot, Nathalie Meuleman, Philippe Mineur, Barbara Dessars, Hakim El Housni, Dominique Bron, Laurence Lagneaux, Basile Stamatopoulos

Open access · bronzeAbstract read
In one paragraph

Article in Epigenetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 18 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

9 authors at 3 institutions in 3 countries.

Michaël Van Dammea Laboratory of Clinical Cell Therapy; Faculty of Medicine; Institut Jules Bordet ; Université Libre de Bruxelles (ULB) ; Brussels , Belgium.
Emerence Crompot
Nathalie Meuleman
Philippe Mineur
Barbara Dessars
Hakim El Housni
Dominique Bron
Laurence Lagneaux
Basile Stamatopoulos
Université Libre de Bruxelles · BEInstitut Jules Bordet · BEGrand Charleroi Hospital · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Histone deacetylases (HDAC) play a crucial role in transcriptional regulation and are often deregulated in many cancers. However, global HDAC enzymatic activity has never been investigated in Chronic Lymphocytic Leukemia (CLL). We measured HDAC activity in protein extracts from CD19+ B-cells purified from 114 CLL patients with a median follow-up of 91 months (range: 11-376). HDAC activity was equivalent in CLL and normal B-cells but higher in patients who died during the study than in living patients (152.1 vs. 65.04 pmol; P = 0.0060). Furthermore, HDAC activity correlated with treatment-free survival (TFS; P = 0.0156) and overall survival (OS; P < 0.0001): patients with low HDAC activity (n = 75) had a median TFS and OS of 101 and > 376 months, respectively, whereas patients with high HDAC activity (n = 39) had a median TFS and OS of 47 and 137 months, respectively. Multivariate analyses indicated that HDAC activity is an independent predictor of OS (hazard ratio = 7.68; P = 0.0017). Finally, HDAC activity increased after B-cell receptor stimulation using IgM, suggesting a role for microenvironment stimuli (n = 10; P = 0.0371). In conclusion, high HDAC activity in CLL B-cells is associated with shorter TFS and OS and is an independent marker of OS, refining the use of other prognostic factors. This work provides a biological base for the use of HDAC inhibitors in CLL treatment.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorB-LymphocytesCase-Control StudiesHistone DeacetylasesHistonesHumansLeukemia, Lymphocytic, Chronic, B-CellMiddle AgedPrognosisProportional Hazards ModelsTumor Cells, CulturedBiomarkers, TumorHistone DeacetylasesHistonesB2M, Beta-2-microglobulinBCR, B cell receptorchronic lymphocytic leukemiaCLL, Chronic lymphocytic leukemiaenzymatic activityFCR Fludarabine-cyclophosphamide-rituximabHDACHDAC, Histone deacetylaseHDACi, HDAC inhibitorHR Hazard ratioIgHV, Immunoglobulin heavy-chain variable-regionLDT, Lymphocyte doubling timeLPL, Lipoprotein lipaseMSC, Mesenchymal stromal cellNF-κB, Nuclear factor κBOS, Overall survivalprognosisSAHA, Suberoylanilide hydroxamic acidsCD23, Soluble CD23SIRT, SirtuinSirtuinTFS, Treatment-free survivalVPA, Valproic acidZAP70, Zeta-chain-associated protein kinase 70

Identifiers

PMID25437053
PMCPMC4622440
OpenAlexW2067168026

What OpenQuestion holds

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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.