Evidence map›Paper›PMID 9053449›Full record

ArticleThe Journal of experimental medicine1997

Involvement of Egr-1/RelA synergy in distinguishing T cell activation from tumor necrosis factor-alpha-induced NF-kappa B1 transcription.

P C Cogswell, M W Mayo, A S Baldwin

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

21 citing papers in PubMed, 66 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Egr-1 deficiency protects from renal inflammation and fibrosis.Journal of molecular medicine (Berlin, Germany) · 2016
    Article
  5. Article
  6. Article
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  8. Article
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  10. Posttranscriptional regulation of interleukin-10 expression by hsa-miR-106a.Proceedings of the National Academy of Sciences of the United States of America · 2009
    Article
  11. Regulation of the neuronal proteasome by Zif268 (Egr1).The Journal of neuroscience : the official journal of the Society for Neuroscience · 2006
    Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Expression of Egr-1 in late stage emphysema.The American journal of pathology · 2000
    Article
  17. Article
  18. Review
  19. Article
  20. 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

3 authors at 2 institutions in 1 country.

P C CogswellLineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill 27599-7295, USA.
M W Mayo
A S Baldwin
UNC Lineberger Comprehensive Cancer CenterUniversity of North Carolina at Chapel Hill · US

Funding

Unexpected Nucleosomal Functions for the IKKsR37AI035098 · NIAID · UNIV OF NORTH CAROLINA CHAPEL HILL · PI BALDWIN, ALBERT SIDNEY · 2004 to 2013
$3.2M
TNF SIGNALING--ACTIVATION OF NF-KB AND GENE EXPRESSIONR01AI035098 · NIAID · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI BALDWIN, ALBERT SIDNEY · 1994 to 2003
$981k
BC1-2 REGULATION AND MODULATION BY RAS, P53 AND C/EBPF32CA069790 · NCI · UNIVERSITY OF NORTH CAROLINA CHAPEL HILL · PI MAYO, MARTY W · 1996 to 1996
–
NCI NIH HHS 1F32-CA69790-01NCI NIH HHS F32 CA069790NIAID NIH HHS AI35098NIAID NIH HHS R01 AI035098NIAID NIH HHS R37 AI035098
6 · The paper itself

Abstract

NF-kappa B is an important transcription factor required for T cell proliferation and other immunological functions. The NF-kappa B1 gene encodes a 105-kD protein that is the precursor of the p50 component of NF-kappa B. Previously, we and others have demonstrated that NF-kappa B regulates the NF-kappa B1 gene. In this manuscript we have investigated the molecular mechanisms by which T cell lines stimulated with phorbol 12-myristate 13-acetate (PMA) and phytohemagglutin (PHA) display significantly higher levels of NF-kappa B1 encoding transcripts than cells stimulated with tumor necrosis factor-alpha, despite the fact that both stimuli activate NF-kappa B. Characterization of the NF-kappa B1 promoter identified an Egr-1 site which was found to be essential for both the PMA/PHA-mediated induction as well as the synergistic activation observed after the expression of the RelA subunit of NF-kappa B and Egr-1. Furthermore, Egr-1 induction was required for endogenous NF-kappa B1 gene expression, since PMA/PHA-stimulated T cell lines expressing antisense Egr-1 RNA were inhibited in their ability to upregulate NF-kappa B1 transcription. Our studies indicate that transcriptional synergy mediated by activation of both Egr-1 and NF-kappa B may have important ramifications in T cell development by upregulating NF-kappa B1 gene expression.

Indexed as

Immediate-Early ProteinsLymphocyte ActivationBinding SitesDNADNA-Binding ProteinsEarly Growth Response Protein 1Gene Expression RegulationHumansNF-kappa BPromoter Regions, GeneticRNA, MessengerTetradecanoylphorbol AcetateT-LymphocytesTranscription Factor RelATranscription FactorsTranscription, GeneticDNADNA-Binding ProteinsEarly Growth Response Protein 1EGR1 protein, humanImmediate-Early ProteinsNF-kappa BRNA, MessengerTetradecanoylphorbol AcetateTranscription Factor RelATranscription FactorsTumor Necrosis Factor-alpha

Identifiers

PMID9053449
PMCPMC2196044
OpenAlexW2145582353

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.