Evidence map›Paper›PMID 36893259›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2023

KMT2D acetylation by CREBBP reveals a cooperative functional interaction at enhancers in normal and malignant germinal center B cells.

Sofija Vlasevska, Laura Garcia-Ibanez, Romain Duval, Antony B Holmes, Rahat Jahan, Bowen Cai, Andrew Kim, Tongwei Mo, Katia Basso, Rajesh K Soni and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 14 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Sofija VlasevskaInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Laura Garcia-IbanezInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Romain DuvalInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Antony B HolmesInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Rahat JahanInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Bowen CaiInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Andrew KimInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Tongwei MoInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Katia BassoInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Rajesh K SoniProteomics and Macromolecular Crystallography Shared Resource, Columbia University, New York, NY 10032.ORCID 0000-0002-4556-4358
Govind BhagatDepartment of Pathology and Cell Biology, Columbia University, New York, NY 10032.ORCID 0000-0001-6250-048X
Riccardo Dalla-FaveraInstitute for Cancer Genetics, Columbia University, New York, NY 10032.
Laura PasqualucciInstitute for Cancer Genetics, Columbia University, New York, NY 10032.ORCID 0000-0001-6819-7370
Cancer Genetics (United States) · USColumbia University Irving Medical Center · US

Funding

Tumor Biology and Microenvironment ProgramP30CA013696 · NCI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Anil K Rustgi · 1985 to 2026
$115.3M
From pathogenesis to new therapeutic targets in Diffuse Large B cell LymphomaR35CA210105 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Riccardo Dalla-Favera · 2016 to 2026
$10.0M
Role of MLL2 Gene Inactivation in B cell Non Hodgkin LymphomaR01CA172492 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI PASQUALUCCI, LAURA · 2013 to 2022
$3.6M
Role of CREBBP missense mutations in lymphomagenesisR01CA260176 · NCI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Riccardo Dalla-Favera · 2022 to 2026
$2.3M
Role of FOXO1 mutations in the pathogenesis of B cell non-Hodgkin lymphomasR01CA207963 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI DOMINGUEZ-SOLA, DAVID · 2018 to 2022
$2.0M
NCI NIH HHS P30 CA013696NCI NIH HHS R01 CA172492NCI NIH HHS R01 CA207963NCI NIH HHS R01 CA260176NCI NIH HHS R35 CA210105
6 · The paper itself

Abstract

Heterozygous inactivating mutations of the KMT2D methyltransferase and the CREBBP acetyltransferase are among the most common genetic alterations in B cell lymphoma and co-occur in 40 to 60% of follicular lymphoma (FL) and 30% of EZB/C3 diffuse large B cell lymphoma (DLBCL) cases, suggesting they may be coselected. Here, we show that combined germinal center (GC)-specific haploinsufficiency of

Indexed as

Lymphoma, FollicularLymphoma, Large B-Cell, DiffuseAcetylationAnimalsB-LymphocytesCREB-Binding ProteinDNA-Binding ProteinsGerminal CenterHumansMiceMutationNeoplasm ProteinsProtein Processing, Post-TranslationalCREB-Binding ProteinCREBBP protein, humanCrebbp protein, mouseDNA-Binding ProteinsKMT2D protein, humanNeoplasm ProteinsacetylationB cell lymphomaCREBBPgerminal centerKMT2D

Identifiers

PMID36893259
PMCPMC10089214
OpenAlexW4323656746

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.