Evidence map›Paper›PMID 29051483›Full record

ArticleNature communications2017

Ets transcription factor GABP controls T cell homeostasis and immunity.

Chong T Luo, Hatice U Osmanbeyoglu, Mytrang H Do, Michael R Bivona, Ahmed Toure, Davina Kang, Yuchen Xie, Christina S Leslie, Ming O Li

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
0.4field-weighted citation impact, top 38% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

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  16. Specific subfamilies of transposable elements contribute to different domains of T lymphocyte enhancers.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  17. Article
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

9 authors at 1 institution in 1 country.

Chong T LuoImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.ORCID http://orcid.org/0000-0002-3477-5969
Hatice U OsmanbeyogluComputational Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Mytrang H DoImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Michael R BivonaImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Ahmed ToureImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Davina KangImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Yuchen XieLouis V. Gerstner Jr. Graduate School of Biomedical Sciences, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Christina S LeslieComputational Biology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA.
Ming O LiImmunology Program, Memorial Sloan Kettering Cancer Center, New York, NY, 10065, USA. lim@mskcc.org.
Memorial Sloan Kettering Cancer Center · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Nutrient Sensing and mTORC1 Signaling in the Control of Regulatory T Cell Generation and FunctionR01AI102888 · NIAID · SLOAN-KETTERING INST CAN RESEARCH · PI LI, MING · 2014 to 2022
$4.3M
Algorithms to link signaling pathways with transcriptional programs for precision medicineK99CA207871 · NCI · SLOAN-KETTERING INST CAN RESEARCH · PI OSMANBEYOGLU, HATICE ULKU · 2016 to 2017
$270k
Howard Hughes Medical InstituteNCI NIH HHS K99 CA207871NCI NIH HHS P30 CA008748NIAID NIH HHS R01 AI102888
6 · The paper itself

Abstract

Peripheral T cells are maintained in the absence of vigorous stimuli, and respond to antigenic stimulation by initiating cell cycle progression and functional differentiation. Here we show that depletion of the Ets family transcription factor GA-binding protein (GABP) in T cells impairs T-cell homeostasis. In addition, GABP is critically required for antigen-stimulated T-cell responses in vitro and in vivo. Transcriptome and genome-wide GABP-binding site analyses identify GABP direct targets encoding proteins involved in cellular redox balance and DNA replication, including the Mcm replicative helicases. These findings show that GABP has a nonredundant role in the control of T-cell homeostasis and immunity.

Indexed as

Adaptive ImmunityAnimalsAntigensBinding SitesCD4 AntigensCell ProliferationCells, CulturedDNA ReplicationGA-Binding Protein Transcription FactorHomeostasisLymphocyte ActivationMiceMice, Inbred C57BLMice, KnockoutMinichromosome Maintenance ProteinsT-LymphocytesAntigensCD4 AntigensGA-Binding Protein Transcription FactorGabpa protein, mouseMinichromosome Maintenance Proteins

Identifiers

PMID29051483
PMCPMC5648787
OpenAlexW2765773273

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.