Evidence map›Paper›PMID 25204569›Full record

ArticleLeukemia2015

Prognostic and biologic significance of DNMT3B expression in older patients with cytogenetically normal primary acute myeloid leukemia.

C Niederwieser, J Kohlschmidt, S Volinia, S P Whitman, K H Metzeler, A-K Eisfeld, K Maharry, P Yan, D Frankhouser, H Becker and 17 more

Open access · bronzeAbstract read
In one paragraph

Article in Leukemia, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

52 citing papers in PubMed, 76 citations in OpenAlex.

  1. Trial
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  3. Expression and prognostic impact of lncRNAs in acute myeloid leukemia.Proceedings of the National Academy of Sciences of the United States of America · 2014
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  8. Roles ofClinical Medicine Insights. Oncology · 2024
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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

27 authors at 9 institutions in 1 country.

C NiederwieserThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
J Kohlschmidt1] The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA [2] Alliance for Clinical Trials in Oncology Statistics and Data Center, Mayo Clinic, Rochester, MN, USA.
S VoliniaThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
S P WhitmanThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
K H MetzelerThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
A-K EisfeldThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
K Maharry1] The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA [2] Alliance for Clinical Trials in Oncology Statistics and Data Center, Mayo Clinic, Rochester, MN, USA.
P YanThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
D FrankhouserThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
H BeckerThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
S SchwindThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
A J CarrollDepartment of Genetics, University of Alabama at Birmingham, Birmingham, AL, USA.
D Nicolet1] The Ohio State University Comprehensive Cancer Center, Columbus, OH, USA [2] Alliance for Clinical Trials in Oncology Statistics and Data Center, Mayo Clinic, Rochester, MN, USA.
J H MendlerThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
J P CurfmanThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
Y-Z WuThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
M R BaerDepartment of Medicine and Greenebaum Cancer Center, University of Maryland, Baltimore, MD, USA.
B L PowellComprehensive Cancer Center of Wake Forest University, Winston-Salem, NC, USA.
J E KolitzMonter Cancer Center, Hofstra North Shore-Long Island Jewish School of Medicine, Lake Success, NY, USA.
J O MooreDepartment of Medicine, Duke University Medical Center, Durham, NC, USA.
T H CarterDepartment of Internal Medicine, University of Iowa, Iowa City, IA, USA.
R BundschuhDepartments of Physics and Chemistry and Biochemistry, The Ohio State University, Columbus, OH, USA.
R A LarsonDepartment of Medicine, University of Chicago Medical Center, Chicago, IL, USA.
R M StoneDepartment of Medical Oncology, Dana Farber Cancer Institute, Boston, MA, USA.
K MrózekThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
G MarcucciThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
C D BloomfieldThe Ohio State University Comprehensive Cancer Center, Columbus, OH, USA.
The Ohio State University · USDana-Farber Cancer Institute · USDuke Medical Center · USMayo Clinic · USUniversity of Alabama at Birmingham · USUniversity of Chicago Medical Center · USUniversity of Iowa · USUniversity of Maryland, Baltimore · USWake Forest University · US

Funding

Member Site CoreU10CA180821 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI Evanthia Galanis · 2014 to 2026
$177.3M
CANCER AND LEUKEMIA GROUP B MINORITY SATELLITE SUPPLEMENU10CA031946 · NCI · UNIVERSITY OF CHICAGO · PI BERTAGNOLLI, MONICA M · 1985 to 2013
$158.4M
Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Jennifer A. Woyach · 1985 to 2026
$132.3M
Statistics CoreU10CA180882 · NCI · MAYO CLINIC ROCHESTER · PI Sumithra Jay Mandrekar · 2014 to 2026
$115.0M
CANCER &LEUKEMIA GROUP B STATISTICAL CENTERU10CA033601 · NCI · UNIVERSITY OF NEBRASKA MEDICAL CENTER · PI SARGENT, DANIEL J. · 1985 to 2013
$69.4M
SPORE Leukemia Tissue BankP50CA140158 · NCI · OHIO STATE UNIVERSITY · PI MARCUCCI, GUIDO · 2009 to 2013
$11.2M
Cancer and Leukemia Group B Human Specimen RepositoriesU24CA114725 · NCI · UNIVERSITY OF CHICAGO · PI BERTAGNOLLI, MONICA M · 2005 to 2014
$11.1M
Cancer and Leukemia Group B - Leukemia Correlative SciencesU10CA101140 · NCI · OHIO STATE UNIVERSITY · PI MARCUCCI, GUIDO · 2003 to 2013
$10.3M
OSU as Network Lead Academic Participating Site for the NCI NCTNU10CA180850 · NCI · OHIO STATE UNIVERSITY · PI BLUM, KRISTIE A, CHAKRAVARTI, ARNAB · 2014 to 2018
$6.8M
Cancer and Leukemia Group B - The Ohio State UniversityU10CA077658 · NCI · OHIO STATE UNIVERSITY · PI BLOOMFIELD, CLARA D · 1998 to 2013
$6.0M
ITSC for Leukemia: Novel Molecular Strategies for NCTN: "Individualized" TherapieU10CA180861 · NCI · OHIO STATE UNIVERSITY · PI BLOOMFIELD, CLARA D, MARCUCCI, GUIDO · 2014 to 2018
$3.4M
Integrative Training in Biomedical SystemsT32GM068412 · NIGMS · OHIO STATE UNIVERSITY · PI PARVIN, JEFFREY D · 2005 to 2020
$2.4M
NCI NIH HHS CA101140NCI NIH HHS CA114725NCI NIH HHS CA129657NCI NIH HHS CA140158NCI NIH HHS CA16058NCI NIH HHS CA31946NCI NIH HHS CA33601NCI NIH HHS CA77658NCI NIH HHS P30 CA016058NCI NIH HHS P50 CA140158NCI NIH HHS R21 CA129657NCI NIH HHS U10 CA031946NCI NIH HHS U10 CA033601NCI NIH HHS U10 CA077658NCI NIH HHS U10 CA101140NCI NIH HHS U10 CA180821NCI NIH HHS U10 CA180850NCI NIH HHS U10 CA180861NCI NIH HHS U10 CA180882NCI NIH HHS U24 CA114725NIGMS NIH HHS T32 GM068412
6 · The paper itself

Abstract

DNMT3B encodes a DNA methyltransferase implicated in aberrant epigenetic changes contributing to leukemogenesis. We tested whether DNMT3B expression, measured by NanoString nCounter assay, associates with outcome, gene and microRNA expression and DNA methylation profiles in 210 older (⩾60 years) adults with primary, cytogenetically normal acute myeloid leukemia (CN-AML). Patients were dichotomized into high versus low expressers using median cut. Outcomes were assessed in the context of known CN-AML prognosticators. Gene and microRNA expression, and DNA methylation profiles were analyzed using microarrays and MethylCap-sequencing, respectively. High DNMT3B expressers had fewer complete remissions (CR; P=0.002) and shorter disease-free (DFS; P=0.02) and overall (OS; P<0.001) survival. In multivariable analyses, high DNMT3B expression remained an independent predictor of lower CR rates (P=0.04) and shorter DFS (P=0.04) and OS (P=0.001). High DNMT3B expression associated with a gene expression profile comprising 363 genes involved in differentiation, proliferation and survival pathways, but with only four differentially expressed microRNAs (miR-133b, miR-148a, miR-122, miR-409-3p) and no differential DNA methylation regions. We conclude that high DNMT3B expression independently associates with adverse outcome in older CN-AML patients. Gene expression analyses suggest that DNMT3B is involved in the modulation of several genes, although the regulatory mechanisms remain to be investigated to devise therapeutic approaches specific for these patients.

Indexed as

Gene Expression Regulation, LeukemicAgedAged, 80 and overAge FactorsCytarabineDaunorubicinDNA (Cytosine-5-)-MethyltransferasesDNA MethylationDNA Methyltransferase 3BFemaleGene Expression ProfilingHumansInduction ChemotherapyKaryotypingLeukemia, Myeloid, AcuteMaleCytarabineDaunorubicinDNA (Cytosine-5-)-MethyltransferasesDNA Methyltransferase 3BMicroRNAs

Identifiers

PMID25204569
PMCPMC4351165
OpenAlexW2059981122

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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.