Evidence map›Paper›PMID 26437030›Full record

ArticleNature genetics2015

DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control.

Helene Kretzmer, Stephan H Bernhart, Wei Wang, Andrea Haake, Marc A Weniger, Anke K Bergmann, Matthew J Betts, Enrique Carrillo-de-Santa-Pau, Gero Doose, Jana Gutwein and 50 more

Open access · greenAbstract read
In one paragraph

Article in Nature genetics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed
12.9field-weighted citation impact, top 1% 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

92 citing papers in PubMed, 150 citations in OpenAlex.

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  14. Subtyping Burkitt Lymphoma by DNA Methylation.Genes, chromosomes & cancer · 2025
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32 more citing papers are in PubMed but not listed here.

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

60 authors at 8 institutions in 5 countries.

Helene Kretzmer *Transcriptome Bioinformatics, LIFE Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany.
Stephan H Bernhart *Transcriptome Bioinformatics, LIFE Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany.
Wei Wang *German Cancer Research Center (DKFZ), Division Molecular Genetics, Heidelberg, Germany.
Andrea Haake *German ICGC MMML-Seq-project.
Marc A Weniger *German ICGC MMML-Seq-project.
Anke K Bergmann *Institute of Human Genetics, Christian-Albrechts-University, Kiel, Germany.
Matthew J BettsCell Networks, Bioquant, University of Heidelberg, Heidelberg, Germany.
Enrique Carrillo-de-Santa-PauBLUEPRINT project.
Gero DooseTranscriptome Bioinformatics, LIFE Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany.
Jana GutweinInstitute of Human Genetics, Christian-Albrechts-University, Kiel, Germany.
Julia RichterGerman ICGC MMML-Seq-project.
Volker HovestadtGerman Cancer Research Center (DKFZ), Division Molecular Genetics, Heidelberg, Germany.
Bingding HuangDeutsches Krebsforschungszentrum Heidelberg (DKFZ), Division Theoretical Bioinformatics, Heidelberg, Germany.
Daniel RicoBLUEPRINT project.
Frank JühlingTranscriptome Bioinformatics, LIFE Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany.
Julia KolarovaInstitute of Human Genetics, Christian-Albrechts-University, Kiel, Germany.
Qianhao LuCell Networks, Bioquant, University of Heidelberg, Heidelberg, Germany.
Christian OttoTranscriptome Bioinformatics, LIFE Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany.
Rabea WagenerGerman ICGC MMML-Seq-project.
Judith ArnoldsDepartment of Otorhinolaryngology, University of Duisburg-Essen, Essen, Germany.
Birgit BurkhardtGerman ICGC MMML-Seq-project.
Alexander ClaviezGerman ICGC MMML-Seq-project.
Hans G DrexlerLeibniz-Institut DSMZ, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Sonja EberthGerman ICGC MMML-Seq-project.
Roland EilsGerman ICGC MMML-Seq-project.
Paul FlicekBLUEPRINT project.
Siegfried HaasGerman ICGC MMML-Seq-project.
Michael HummeGerman ICGC MMML-Seq-project.
Dennis KarschGerman ICGC MMML-Seq-project.
Hinrik H D KerstensBLUEPRINT project.
Wolfram KlapperGerman ICGC MMML-Seq-project.
Markus KreuzGerman ICGC MMML-Seq-project.
Chris LawerenzGerman ICGC MMML-Seq-project.
Dido LenzekGerman ICGC MMML-Seq-project.
Markus LoefflerGerman ICGC MMML-Seq-project.
Cristina LópezGerman ICGC MMML-Seq-project.
Roderick A F MacLeodLeibniz-Institut DSMZ, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany.
Joost H A MartensBLUEPRINT project.
Marta KulisBLUEPRINT project.
José Ignacio Martín-SuberoBLUEPRINT project.
Peter MöllerGerman ICGC MMML-Seq-project.
Inga NageGerman ICGC MMML-Seq-project.
Simone PicelliGerman Cancer Research Center (DKFZ), Division Molecular Genetics, Heidelberg, Germany.
Inga VaterGerman ICGC MMML-Seq-project.
Marius RohdeGerman ICGC MMML-Seq-project.
Philip RosenstielGerman ICGC MMML-Seq-project.
Maciej RosolowskiGerman ICGC MMML-Seq-project.
Robert B RussellCell Networks, Bioquant, University of Heidelberg, Heidelberg, Germany.
Markus SchilhabelGerman ICGC MMML-Seq-project.
Matthias SchlesnerGerman ICGC MMML-Seq-project.
Peter F StadlerTranscriptome Bioinformatics, LIFE Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany.
Monika SzczepanowskiGerman ICGC MMML-Seq-project.
Lorenz TrümperGerman ICGC MMML-Seq-project.
Hendrik G StunnenbergBLUEPRINT project.
Ralf KüppersGerman ICGC MMML-Seq-project.
Ole AmmerpohlGerman ICGC MMML-Seq-project.
Peter LichterGerman ICGC MMML-Seq-project.
Reiner SiebertGerman ICGC MMML-Seq-project.
Steve HoffmannTranscriptome Bioinformatics, LIFE Research Center for Civilization Diseases, University of Leipzig, Leipzig, Germany.
Bernhard RadlwimmerGerman ICGC MMML-Seq-project.
German Institute of Development and Sustainability · DEChristian-Albrechts-Universität zu Kiel · DEGerman Cancer Research Center · DERadboud University Nijmegen · NLEuropean Bioinformatics Institute · GBSanta Fe Institute · USHeidelberg University · DEUniversity of Duisburg-Essen · DE

Funding

Wellcome Trust 095908
6 · The paper itself

Abstract

Although Burkitt lymphomas and follicular lymphomas both have features of germinal center B cells, they are biologically and clinically quite distinct. Here we performed whole-genome bisulfite, genome and transcriptome sequencing in 13 IG-MYC translocation-positive Burkitt lymphoma, nine BCL2 translocation-positive follicular lymphoma and four normal germinal center B cell samples. Comparison of Burkitt and follicular lymphoma samples showed differential methylation of intragenic regions that strongly correlated with expression of associated genes, for example, genes active in germinal center dark-zone and light-zone B cells. Integrative pathway analyses of regions differentially methylated in Burkitt and follicular lymphomas implicated DNA methylation as cooperating with somatic mutation of sphingosine phosphate signaling, as well as the TCF3-ID3 and SWI/SNF complexes, in a large fraction of Burkitt lymphomas. Taken together, our results demonstrate a tight connection between somatic mutation, DNA methylation and transcriptional control in key B cell pathways deregulated differentially in Burkitt lymphoma and other germinal center B cell lymphomas.

Indexed as

DNA MethylationMutationAdolescentAdultAgedB-LymphocytesBurkitt LymphomaCell Line, TumorChildChild, PreschoolFemaleGenome, HumanGerminal CenterHigh-Throughput Nucleotide SequencingHumansLymphoma, FollicularMYC protein, humanOncogene Proteins, FusionProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-myc

Identifiers

PMID26437030
PMCPMC5444523
OpenAlexW1878239255

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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.