Evidence map›Paper›PMID 22167720›Full record

ReviewJournal of leukocyte biology2012

Cell type- and stimulus-specific mechanisms for post-transcriptional control of neutrophil chemokine gene expression.

Thomas Hamilton, Xiaoxia Li, Michael Novotny, Paul G Pavicic, Shyamasree Datta, Chenyang Zhao, Justin Hartupee, Dongxu Sun

Open access · bronzeAbstract readReview
In one paragraph

Review in Journal of leukocyte biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Regulation of the mRNA half-life in breast cancer.World journal of clinical oncology · 2014
    Review
  14. Article
  15. Review
  16. Article
  17. Post-transcriptional control of cytokine gene expression in health and disease.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2014
    Article
  18. Article
  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

8 authors at 2 institutions in 1 country.

Thomas HamiltonCleveland Clinic Foundation, 9500 Euclid Ave., Cleveland, OH 44195-0001, USA. hamiltt@ccf.org
Xiaoxia Li
Michael Novotny
Paul G Pavicic
Shyamasree Datta
Chenyang Zhao
Justin Hartupee
Dongxu Sun
Cleveland Clinic · USWashington University in St. Louis · 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
Molecular Mechanisms for IL-25-mediated Th2 ResponsesR01HL098935 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI LI, XIAOXIA · 2010 to 2010
$359k
NCI NIH HHS CA39621NCI NIH HHS R01 CA039621NHLBI NIH HHS HL098935NHLBI NIH HHS R01 HL098935NIGMS NIH HHS T32 GM007250
6 · The paper itself

Abstract

mRNAs encoding inflammatory chemokines that recruit neutrophils frequently exhibit short half-lives that serve to limit their expression under inappropriate conditions but are often prolonged to ensure adequate levels during inflammatory response. Extracellular stimuli that modulate the stability of such mRNAs may be the same as the transcriptional activator, as is the case with TLR ligands, or may cooperate with independent transcriptional stimuli, as with IL-17, which extends the half-life of TNF-induced transcripts. These different stimuli engage independent signaling pathways that target different instability mechanisms distinguished by dependence on different regulatory nucleotide sequence motifs within the 3'UTRs, which involve that action of different mRNA-binding proteins. The selective use of these pathways by different stimuli and in distinct cell populations provides the potential for tailoring of chemokine expression patterns to meet specific needs in different pathophysiologic circumstances.

Indexed as

RNA Processing, Post-TranscriptionalAnimalsChemokinesGene ExpressionGene Expression RegulationHumansInflammationInterleukin-17NeutrophilsRNA, MessengerRNA StabilitySignal TransductionToll-Like ReceptorsTristetraprolinChemokinesInterleukin-17RNA, MessengerToll-Like ReceptorsTristetraprolin

Identifiers

PMID22167720
PMCPMC3409633
OpenAlexW2141047653

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.