Evidence map›Paper›PMID 18411265›Full record

ArticleThe Journal of biological chemistry2008

Interleukin 1alpha-induced NFkappaB activation and chemokine mRNA stabilization diverge at IRAK1.

Justin Hartupee, Xiaoxia Li, Thomas Hamilton

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
2.6field-weighted citation impact, top 9% 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

29 citing papers in PubMed, 44 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Paeoniflorin Inhibits LPS-Induced Activation of Splenic CD4Evidence-based complementary and alternative medicine : eCAM · 2022
    Article
  5. Article
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  7. Article
  8. Targeting Myddosome Signaling in Waldenström's Macroglobulinemia with the Interleukin-1 Receptor-Associated Kinase 1/4 Inhibitor R191.Clinical cancer research : an official journal of the American Association for Cancer Research · 2018
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Article
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  18. Article
  19. NF-kappaB dysregulation in microRNA-146a-deficient mice drives the development of myeloid malignancies.Proceedings of the National Academy of Sciences of the United States of America · 2011
    Article
  20. The kinase activity of interleukin-1 receptor-associated kinase 2 is essential for lipopolysaccharide-mediated cytokine and chemokine mRNA stability and translation.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2011
    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 1 institution in 1 country.

Justin HartupeeDepartment of Immunology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
Xiaoxia Li
Thomas Hamilton
Cleveland Clinic · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM007250 · NIGMS · CASE WESTERN RESERVE UNIVERSITY · PI HUANG, ALEX YEE-CHEN · 1985 to 2023
$33.4M
Post-transcriptional control of inflammatory gene expressionR01CA039621 · NCI · DUKE UNIVERSITY · PI HAMILTON, THOMAS A. · 1985 to 2013
$3.6M
NCI NIH HHS CA39621NCI NIH HHS R01 CA039621NIGMS NIH HHS T32 GM007250NIGMS NIH HHS T32GM007250
6 · The paper itself

Abstract

Interleukin 1alpha (IL-1alpha) is capable of driving pro-inflammatory gene expression through both the initiation of transcription and by prolonging the half-life of short-lived mRNAs. Although the signaling events linking the IL-1 receptor to the activation of NFkappaB and the initiation of transcription have been well characterized, less is known about the signaling events linking to mRNA stabilization. As a model to study the control of mRNA stability we have used the mouse chemokine KC, expression of which requires both NFkappaB-driven transcription and stabilization of the constitutively unstable mRNA. We have evaluated the role of signaling adaptors known to play a role in IL-1alpha-driven NFkappaB activation in the generation of mRNA stability. Surprisingly, although TRAF6 is essential for NFkappaB activation, it is not required for IL-1alpha-induced mRNA stabilization. IRAK1, which is recognized to function upstream of TRAF6, is required for both mRNA stabilization and activation of NFkappaB. Consistent with the previous findings, the TRAF6 interaction sites in IRAK1 are required for NFkappaB activation but do not play a role in mRNA stabilization. These findings indicate that signals from the IL-1 receptor segregate into at least two separate pathways at the level of IRAK1; one couples through TRAF6 to NFkappaB activation while a second utilizes a TRAF6-independent pathway that is responsible for mRNA stabilization.

Indexed as

AnimalsChemokine CXCL1Gene Expression RegulationHeLa CellsHumansInterleukin-1alphaInterleukin-1 Receptor-Associated KinasesMiceModels, BiologicalNF-kappa BReceptors, Interleukin-1RNA, MessengerRNA StabilitySignal TransductionTNF Receptor-Associated Factor 6Chemokine CXCL1Cxcl1 protein, mouseInterleukin-1alphaInterleukin-1 Receptor-Associated KinasesIRAK1 protein, humanIrak1 protein, mouseNF-kappa BReceptors, Interleukin-1RNA, MessengerTNF Receptor-Associated Factor 6

Identifiers

PMID18411265
PMCPMC3259643
OpenAlexW1998507474

What OpenQuestion holds

Textmetadata
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.