Evidence map›Paper›PMID 23680150›Full record

ArticleCancer cell2013

EZH2 is required for germinal center formation and somatic EZH2 mutations promote lymphoid transformation.

Wendy Béguelin, Relja Popovic, Matt Teater, Yanwen Jiang, Karen L Bunting, Monica Rosen, Hao Shen, Shao Ning Yang, Ling Wang, Teresa Ezponda and 23 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer cell, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 511 papers.

0numbers the graph read from it
0cells of the map it votes in
511citing papers in PubMed
30.8field-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

511 citing papers in PubMed, 832 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

33 authors at 6 institutions in 2 countries.

Wendy BéguelinDivision of Hematology/Oncology, Department of Medicine, Weill Cornell Medical College, New York, NY 10021, USA.
Relja Popovic
Matt Teater
Yanwen Jiang
Karen L Bunting
Monica Rosen
Hao Shen
Shao Ning Yang
Ling Wang
Teresa Ezponda
Eva Martinez-Garcia
Haikuo Zhang
Yupeng Zheng
Sharad K Verma
Michael T McCabe
Heidi M Ott
Glenn S Van Aller
Ryan G Kruger
Yan Liu
Charles F McHugh
David W Scott
Young Rock Chung
Neil Kelleher
Rita Shaknovich
Caretha L Creasy
Randy D Gascoyne
Kwok-Kin Wong
Leandro Cerchietti
Ross L Levine
Omar Abdel-Wahab
Jonathan D Licht
Olivier Elemento
Ari M Melnick
Cornell University · USGlaxoSmithKline (United States) · USNorthwestern University · USMemorial Sloan Kettering Cancer Center · USBC Cancer Agency · CADana-Farber Cancer Institute · US

Funding

Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
StructureP01CA154303 · NCI · DANA-FARBER CANCER INST · PI ECK, MICHAEL J · 2012 to 2021
$17.8M
TRANS-NETWORK PROJECTSU54CA143869 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI MARKO, JOHN F · 2009 to 2013
$12.8M
MUC1-C Oncoprotein Evades Immune Destruction in Non-small Cell Lung CancerR01CA166480 · NCI · DANA-FARBER CANCER INST · PI KUFE, DONALD W., WONG, KWOK KIN · 2012 to 2021
$6.3M
TRAINING PROGRAM IN SIGNAL TRANSDUCTION AND CANCERT32CA070085 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI LEONIDAS C. PLATANIAS · 1997 to 2026
$5.7M
Therapeutic strategies for specific subsets of KRAS mutant lung cancersR01CA140594 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI WONG, KWOK KIN · 2009 to 2017
$4.5M
Molecular Targeting of Diffuse Large B-cell LymphomaR01CA143032 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MELNICK, ARI M. · 2010 to 2014
$2.8M
In vivo analysis of EGFR mutant driven lung cancers responses to radiation therapR01CA122794 · NCI · DANA-FARBER CANCER INST · PI WONG, KWOK KIN · 2006 to 2015
$2.8M
Transcriptional silencing by the BCL6 oncoproteinR01CA104348 · NCI · WEILL MEDICAL COLL OF CORNELL UNIV · PI MELNICK, ARI M. · 2004 to 2014
$2.6M
Role of ASXL1 mutations in myeloid malignanciesK08CA160647 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI ABDEL-WAHAB, OMAR · 2011 to 2015
$849k
NCI NIH HHS 1K08CA160647-01NCI NIH HHS CA143879NCI NIH HHS K08 CA160647NCI NIH HHS P01 CA154303NCI NIH HHS P30 CA060553NCI NIH HHS R01 CA104348NCI NIH HHS R01 CA122794NCI NIH HHS R01 CA140594NCI NIH HHS R01 CA143032NCI NIH HHS R01 CA166480NCI NIH HHS T32 CA070085NCI NIH HHS U54 CA143869
6 · The paper itself

Abstract

The EZH2 histone methyltransferase is highly expressed in germinal center (GC) B cells and targeted by somatic mutations in B cell lymphomas. Here, we find that EZH2 deletion or pharmacologic inhibition suppresses GC formation and functions. EZH2 represses proliferation checkpoint genes and helps establish bivalent chromatin domains at key regulatory loci to transiently suppress GC B cell differentiation. Somatic mutations reinforce these physiological effects through enhanced silencing of EZH2 targets. Conditional expression of mutant EZH2 in mice induces GC hyperplasia and accelerated lymphomagenesis in cooperation with BCL2. GC B cell (GCB)-type diffuse large B cell lymphomas (DLBCLs) are mostly addicted to EZH2 but not the more differentiated activated B cell (ABC)-type DLBCLs, thus clarifying the therapeutic scope of EZH2 targeting.

Indexed as

MutationAnimalsB-LymphocytesCell DifferentiationCell ProliferationCell Transformation, NeoplasticEnhancer of Zeste Homolog 2 ProteinGene DeletionGene Expression Regulation, NeoplasticGerminal CenterHistonesMethylationMicePolycomb Repressive Complex 2Promoter Regions, GeneticProto-Oncogene Proteins c-bcl-2Bcl2 protein, mouseEnhancer of Zeste Homolog 2 ProteinEzh2 protein, mouseHistonesPolycomb Repressive Complex 2Proto-Oncogene Proteins c-bcl-2

Identifiers

PMID23680150
PMCPMC3681809
OpenAlexW2010711123

What OpenQuestion holds

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Read underepoch 390

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.