Evidence map›Paper›PMID 27846393›Full record

ArticleCancer cell2016

Decoding the DNA Methylome of Mantle Cell Lymphoma in the Light of the Entire B Cell Lineage.

Ana C Queirós, Renée Beekman, Roser Vilarrasa-Blasi, Martí Duran-Ferrer, Guillem Clot, Angelika Merkel, Emanuele Raineri, Nuria Russiñol, Giancarlo Castellano, Sílvia Beà and 25 more

Abstract readComment
In one paragraph

Article in Cancer cell, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 68 papers.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed
–field-weighted citation impact
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

68 citing papers in PubMed.

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8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

35 authors.

Ana C QueirósDepartamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona 08036, Spain.
Renée BeekmanInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 08036, Spain.
Roser Vilarrasa-BlasiDepartamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona 08036, Spain.
Martí Duran-FerrerDepartamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona 08036, Spain.
Guillem ClotInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 08036, Spain.
Angelika MerkelCentro Nacional de Análisis Genómico, Parc Científic de Barcelona, Barcelona 08028, Spain.
Emanuele RaineriCentro Nacional de Análisis Genómico, Parc Científic de Barcelona, Barcelona 08028, Spain.
Nuria RussiñolDepartamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona 08036, Spain; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 08036, Spain.
Giancarlo CastellanoInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 08036, Spain.
Sílvia BeàInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 08036, Spain.
Alba NavarroInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 08036, Spain.
Marta KulisDepartamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona 08036, Spain.
Núria Verdaguer-DotDepartamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona 08036, Spain; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 08036, Spain.
Pedro JaresDepartamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona 08036, Spain; Unidad de Genómica, IDIBAPS, Barcelona 08036, Spain.
Anna EnjuanesUnidad de Genómica, IDIBAPS, Barcelona 08036, Spain.
María José CalasanzDepartment of Genetics, University of Navarra, Pamplona 31008, Spain.
Anke BergmannInstitute of Human Genetics, Christian-Albrechts University, Kiel 24105, Germany; Department of Pediatrics, Christian-Albrechts University & University Hospital Schleswig-Holstein, Kiel 24105, Germany.
Inga VaterInstitute of Human Genetics, Christian-Albrechts University, Kiel 24105, Germany.
Itziar SalaverríaInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 08036, Spain.
Harmen J G van de WerkenDepartment of Cell Biology, Erasmus MC, Rotterdam 3015 CN, the Netherlands; Cancer Computational Biology Center, Erasmus MC, Rotterdam 3015 CN, the Netherlands; Department of Urology, Erasmus MC, Rotterdam 3015 CN, the Netherlands.
Wyndham H WilsonLymphoid Malignancies Branch, Center for Cancer Research, National Cancer Institute, Bethesda, MD 20892, USA.
Avik DattaEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton CB10 1SD, UK.
Paul FlicekEuropean Molecular Biology Laboratory, European Bioinformatics Institute (EMBL-EBI), Wellcome Trust Genome Campus, Hinxton CB10 1SD, UK.
Romina RoyoJoint Program on Computational Biology, Barcelona Supercomputing Center (BSC) and Institute of Research in Biomedicine (IRB), Barcelona Science Park, Barcelona 08034, Spain.
Joost MartensMolecular Biology, NCMLS, FNWI, Radboud University, Nijmegen 6500 HB, the Netherlands.
Eva GinéServicio de Hematología, Hospital Clínic, IDIBAPS, Barcelona 08036, Spain.
Armando Lopez-GuillermoServicio de Hematología, Hospital Clínic, IDIBAPS, Barcelona 08036, Spain.
Hendrik G StunnenbergMolecular Biology, NCMLS, FNWI, Radboud University, Nijmegen 6500 HB, the Netherlands.
Wolfram KlapperHematopathology Section and Lymph Node Registry, Christian-Albrecht University, Kiel 24105, Germany.
Christiane PottSecond Medical Department, University Hospital Schleswig-Holstein, Kiel 24116, Germany.
Simon HeathCentro Nacional de Análisis Genómico, Parc Científic de Barcelona, Barcelona 08028, Spain.
Ivo G GutCentro Nacional de Análisis Genómico, Parc Científic de Barcelona, Barcelona 08028, Spain.
Reiner SiebertInstitute of Human Genetics, Christian-Albrechts University, Kiel 24105, Germany.
Elías CampoDepartamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona 08036, Spain; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 08036, Spain; Unidad de Hematopatología, Servicio de Anatomía Patológica, Hospital Clínic, Barcelona 08036, Spain.
José I Martín-SuberoDepartamento de Fundamentos Clínicos, Universitat de Barcelona, Barcelona 08036, Spain; Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 08036, Spain. Electronic address: imartins@clinic.ub.es.

Funding

Worldwide Cancer Research 16-1285
6 · The paper itself

Abstract

We analyzed the in silico purified DNA methylation signatures of 82 mantle cell lymphomas (MCL) in comparison with cell subpopulations spanning the entire B cell lineage. We identified two MCL subgroups, respectively carrying epigenetic imprints of germinal-center-inexperienced and germinal-center-experienced B cells, and we found that DNA methylation profiles during lymphomagenesis are largely influenced by the methylation dynamics in normal B cells. An integrative epigenomic approach revealed 10,504 differentially methylated regions in regulatory elements marked by H3K27ac in MCL primary cases, including a distant enhancer showing de novo looping to the MCL oncogene SOX11. Finally, we observed that the magnitude of DNA methylation changes per case is highly variable and serves as an independent prognostic factor for MCL outcome.

Indexed as

DNA MethylationEnhancer Elements, GeneticB-LymphocytesCell LineageCell Line, TumorComputer SimulationEpigenesis, GeneticEpigenomicsGene Expression Regulation, NeoplasticHigh-Throughput Nucleotide SequencingHumansLymphoma, Mantle-CellSOXC Transcription FactorsSOX11 protein, humanSOXC Transcription FactorsChIP-seqchromatinDNA loopingDNA methylationenhancerepigenomicslymphomamantle cell lymphomaSOX11whole-genome bisulfite sequencing

Identifiers

PMID27846393
PMCPMC5805090

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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.