Evidence map›Paper›PMID 20081860›Full record

ArticleNature genetics2010

Somatic mutations altering EZH2 (Tyr641) in follicular and diffuse large B-cell lymphomas of germinal-center origin.

Ryan D Morin, Nathalie A Johnson, Tesa M Severson, Andrew J Mungall, Jianghong An, Rodrigo Goya, Jessica E Paul, Merrill Boyle, Bruce W Woolcock, Florian Kuchenbauer and 28 more

Open access · greenAbstract read
In one paragraph

Article in Nature genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 908 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
908citing papers in PubMed, 1 pooled it
52.5field-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

908 citing papers in PubMed, 1 synthesis or guideline pooled it, 1,643 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. EZH2 Inhibition and Myeloid Risk: A Feature of On-Target Biology.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. EZH2 and intracellular CaCellular & molecular immunology · 2026
    Article
  13. Review
  14. Molecular Insights and Novel Therapies for Lymphoproliferative Disorders.International journal of molecular sciences · 2026
    Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Review

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

38 authors at 3 institutions in 1 country.

Ryan D MorinGenome Sciences Centre, BC Cancer Agency, Vancouver, British Columbia, Canada.
Nathalie A Johnson
Tesa M Severson
Andrew J Mungall
Jianghong An
Rodrigo Goya
Jessica E Paul
Merrill Boyle
Bruce W Woolcock
Florian Kuchenbauer
Damian Yap
R Keith Humphries
Obi L Griffith
Sohrab Shah
Henry Zhu
Michelle Kimbara
Pavel Shashkin
Jean F Charlot
Marianna Tcherpakov
Richard Corbett
Angela Tam
Richard Varhol
Duane Smailus
Michelle Moksa
Yongjun Zhao
Allen Delaney
Hong Qian
Inanc Birol
Jacqueline Schein
Richard Moore
Robert Holt
Doug E Horsman
Joseph M Connors
Steven Jones
Samuel Aparicio
Martin Hirst
Randy D Gascoyne
Marco A Marra
BC Cancer Agency · CABPS Bioscience (United States)University of British Columbia · CA

Funding

Cancer transcriptome characterization using massively parallel DNA sequencingU24CA143866 · NCI · BRITISH COLUMBIA CANCER AGENCY · PI MARRA, MARCO ANTONIO · 2009 to 2015
$10.9M
CIHRNCI NIH HHS N01 CO012400NCI NIH HHS N01-CO-12400NCI NIH HHS U24 CA143866
6 · The paper itself

Abstract

Follicular lymphoma (FL) and the GCB subtype of diffuse large B-cell lymphoma (DLBCL) derive from germinal center B cells. Targeted resequencing studies have revealed mutations in various genes encoding proteins in the NF-kappaB pathway that contribute to the activated B-cell (ABC) DLBCL subtype, but thus far few GCB-specific mutations have been identified. Here we report recurrent somatic mutations affecting the polycomb-group oncogene EZH2, which encodes a histone methyltransferase responsible for trimethylating Lys27 of histone H3 (H3K27). After the recent discovery of mutations in KDM6A (UTX), which encodes the histone H3K27me3 demethylase UTX, in several cancer types, EZH2 is the second histone methyltransferase gene found to be mutated in cancer. These mutations, which result in the replacement of a single tyrosine in the SET domain of the EZH2 protein (Tyr641), occur in 21.7% of GCB DLBCLs and 7.2% of FLs and are absent from ABC DLBCLs. Our data are consistent with the notion that EZH2 proteins with mutant Tyr641 have reduced enzymatic activity in vitro.

Indexed as

AdultAgedAmino Acid SequenceBase SequenceDNA-Binding ProteinsDNA Mutational AnalysisEnhancer of Zeste Homolog 2 ProteinExonsFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticGenome, HumanGerminal CenterHumansLymphoma, FollicularLymphoma, Large B-Cell, DiffuseDNA-Binding ProteinsEnhancer of Zeste Homolog 2 ProteinEZH2 protein, humanMutant ProteinsPolycomb Repressive Complex 2Transcription FactorsTyrosine

Identifiers

PMID20081860
PMCPMC2850970
OpenAlexW2024373518

What OpenQuestion holds

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LicenceTDM
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.