Evidence map›Paper›PMID 25001468›Full record

ReviewBlood2014

Extracellular nucleotide and nucleoside signaling in vascular and blood disease.

Marco Idzko, Davide Ferrari, Ann-Kathrin Riegel, Holger K Eltzschig

Open access · bronzeAbstract readReview
In one paragraph

Review in Blood, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
11.5field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 131 citations in OpenAlex.

  1. Advances in nucleotide-based P2Y₁ antagonism: implications for cardiovascular therapeutics.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    Review
  2. Article
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  10. P2YPurinergic signalling · 2023
    Review
  11. ENPP1 Immunobiology as a Therapeutic Target.Clinical cancer research : an official journal of the American Association for Cancer Research · 2023
    Review
  12. Article
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13 more citing papers are in PubMed but not listed here.

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

4 authors at 3 institutions in 3 countries.

Marco IdzkoDepartment of Pneumology, Freiburg University Medical Center, Albert-Ludwigs-University, Freiburg, Germany;
Davide FerrariDepartment of Morphology, Surgery and Experimental Medicine, Section of General Pathology, Oncology and Experimental Biology, University of Ferrara, Ferrara, Italy; and.
Ann-Kathrin RiegelOrgan Protection Program, Department of Anesthesiology, University of Colorado School of Medicine, Aurora, CO.
Holger K EltzschigOrgan Protection Program, Department of Anesthesiology, University of Colorado School of Medicine, Aurora, CO.
University of Colorado Denver · USUniversity Medical Center Freiburg · DEUniversity of Ferrara · IT

Funding

Trangenic Mouse Breeding CoreP01HL114457 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ZHANG, YUJIN · 2013 to 2017
$10.0M
Proton Pump Inhibitors for Perioperative Acute Kidney InjuryR01DK097075 · NIDDK · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI ELTZSCHIG, HOLGER K. · 2013 to 2017
$1.7M
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 P01 HL114457NHLBI NIH HHS P01HL114457-01NHLBI NIH HHS R01-HL0921NHLBI NIH HHS R01 HL098294NHLBI NIH HHS R01- HL098294NIDDK NIH HHS R01 DK083385NIDDK NIH HHS R01-DK083385NIDDK NIH HHS R01 DK097075
6 · The paper itself

Abstract

Nucleotides and nucleosides-such as adenosine triphosphate (ATP) and adenosine-are famous for their intracellular roles as building blocks for the genetic code or cellular energy currencies. In contrast, their function in the extracellular space is different. Here, they are primarily known as signaling molecules via activation of purinergic receptors, classified as P1 receptors for adenosine or P2 receptors for ATP. Because extracellular ATP is rapidly converted to adenosine by ectonucleotidase, nucleotide-phosphohydrolysis is important for controlling the balance between P2 and P1 signaling. Gene-targeted mice for P1, P2 receptors, or ectonucleotidase exhibit only very mild phenotypic manifestations at baseline. However, they demonstrate alterations in disease susceptibilities when exposed to a variety of vascular or blood diseases. Examples of phenotypic manifestations include vascular barrier dysfunction, graft-vs-host disease, platelet activation, ischemia, and reperfusion injury or sickle cell disease. Many of these studies highlight that purinergic signaling events can be targeted therapeutically.

Indexed as

Signal TransductionAdenosineAdenosine TriphosphateExtracellular SpaceHematologic DiseasesHumansModels, BiologicalReceptors, Purinergic P1Receptors, Purinergic P2Vascular DiseasesAdenosineAdenosine TriphosphateReceptors, Purinergic P1Receptors, Purinergic P2

Identifiers

PMID25001468
PMCPMC4133480
OpenAlexW1981236618

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.