Evidence map›Paper›PMID 22322265›Full record

ReviewCurrent opinion in critical care2012

Hypoxia signaling during intestinal ischemia and inflammation.

Almut Grenz, Eric Clambey, Holger K Eltzschig

Abstract readReview
In one paragraph

Review in Current opinion in critical care, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
3.0field-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

33 citing papers in PubMed, 60 citations in OpenAlex.

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  11. The pivotal roles of neddylation pathway in immunoregulation.Immunity, inflammation and disease · 2020
    Review
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  17. AFASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2017
    Article
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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

3 authors at 1 institution in 1 country.

Almut GrenzMucosal Inflammation Program, Department of Anesthesiology, University of Colorado, Aurora, Colorado 80045, USA. almut.grenz@ucdenver.edu
Eric Clambey
Holger K Eltzschig
University of Colorado Anschutz Medical Campus · US

Funding

Hypoxia Inducible Factor in Acute Lung InjuryR01HL098294 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI ELTZSCHIG, HOLGER K. · 2011 to 2014
$1.6M
Alternative Mechanisms of Adenosine Receptor ActivationR01DK083385 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI ELTZSCHIG, HOLGER K. · 2010 to 2013
$1.2M
NHLBI NIH HHS R01-HL0921NHLBI NIH HHS R01 HL098294NHLBI NIH HHS R01HL098294NIDDK NIH HHS R01 DK083385NIDDK NIH HHS R01-DK083385
6 · The paper itself

Abstract

purpose of reviewDuring critical illness, alterations of intestinal blood supply and inflammatory activation can result in severe intestinal hypoxia (limited oxygen availability). Conditions of hypoxia lead to the activation of a transcriptional program that is under the control of the transcription factor hypoxia-inducible factor (HIF). In many instances, HIF-dependent alterations of gene expression represent endogenous adaptive responses that dampen pathologic inflammation and could be targeted to treat intestinal injury. RECENT

findingsPost-translational stabilization of the HIF transcription factor and corresponding changes in gene expression are central to the resolution of intestinal injury. Examples for such responses that we discuss in this review include hypoxia-elicited increases in extracellular adenosine production and signaling, particularly through the A2B adenosine receptor, and intestinal protection provided by hypoxia-inducible netrin-1. SUMMARY: The present review focuses on HIF-elicited anti-inflammatory pathways that result in intestinal protection during critical illness. Many of these pathways represent novel therapeutic targets for attenuating multiorgan failure and critical illness. Whereas these therapeutic approaches are currently being investigated in cell culture models or in genetic mouse models, we are optimistic that at least some of these novel targets can be translated from bench to bedside in the near future.

Indexed as

AnimalsCritical IllnessHypoxia-Inducible Factor 1Hypoxia-Inducible Factor 1, alpha SubunitInflammationIntestinal DiseasesIntestinesIschemiaMiceReceptor, Adenosine A2BSignal TransductionHif1a protein, mouseHypoxia-Inducible Factor 1Hypoxia-Inducible Factor 1, alpha SubunitReceptor, Adenosine A2B

Identifiers

PMID22322265
PMCPMC3855266
OpenAlexW2021493915

What OpenQuestion holds

Textmetadata
LicenceTDM
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.