Evidence map›Paper›PMID 21457061›Full record

ReviewExpert opinion on investigational drugs2011

Investigational A₃ adenosine receptor targeting agents.

Balázs Koscsó, Balázs Csóka, Pál Pacher, György Haskó

Abstract readReview
In one paragraph

Review in Expert opinion on investigational drugs, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
–field-weighted citation impact
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

18 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Adenosine AInternational journal of molecular sciences · 2024
    Review
  6. Therapeutic Potential of Highly Selective AMolecules (Basel, Switzerland) · 2022
    Review
  7. Review
  8. AFrontiers in neuroscience · 2021
    Review
  9. AInternational journal of molecular sciences · 2020
    Review
  10. Targeting of G-protein coupled receptors in sepsis.Pharmacology & therapeutics · 2020
    Review
  11. A binding kinetics study of human adenosine ABiochemical pharmacology · 2018
    Article
  12. AMedicinal research reviews · 2018
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Balázs KoscsóUniversity of Medicine and Dentistry of New Jersey, New Jersey Medical School, Department of Surgery, 185 South Orange Avenue, Newark, NJ 07103, USA.
Balázs Csóka
Pál Pacher
György Haskó

Funding

Mechanism of oxidative/nitrosative stress and inflammation-induced tissue injuryZIAAA000375 · NIAAA · NATIONAL INSTITUTE ON ALCOHOL ABUSE AND ALCOHOLISM · PI PACHER, PAL · 2009 to 2025
$27.8M
Purinergic signaling in trauma and sepsisR01GM066189 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI HASKO, GEORGE · 2002 to 2020
$4.7M
Adenosine in trauma and sepsisR56GM066189 · NIGMS · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI HASKO, GYORGY · 2007 to 2007
$272k
Intramural NIH HHS Z99 AA999999Intramural NIH HHS ZIA AA000375NIGMS NIH HHS R01 GM066189NIGMS NIH HHS R01GM66189NIGMS NIH HHS R56 GM066189
6 · The paper itself

Abstract

introductionAdenosine is an endogenous nucleoside that accumulates in the extracellular space in response to metabolic stress and cell damage. Extracellular adenosine is a signaling molecule that signals by activating four GPCRs: the A(1), A(2A), A(2B) and A(3) receptors. Since the discovery of A(3) adenosine receptors, accumulating evidence has identified these receptors as potential targets for therapeutic intervention. AREAS COVERED: A(3) adenosine receptors are expressed on the surface of most immune cell types, including neutrophils, macrophages, dendritic cells, lymphocytes and mast cells. A(3) adenosine receptor activation on immune cells governs a broad array of immune cell functions, which include cytokine production, degranulation, chemotaxis, cytotoxicity, apoptosis and proliferation. In accordance with their multitudinous immunoregulatory actions, targeting A(3) adenosine receptors has been shown to impact the course of a wide spectrum of immune-related diseases, such as asthma, rheumatoid arthritis, cancer, ischemia and inflammatory disorders. EXPERT OPINION: Given the existence of both preclinical and early clinical data supporting the utility of A(3) adenosine receptor ligands in treating immune-related diseases, further development of A(3) adenosine receptor ligands is anticipated.

Indexed as

Adenosine A3 Receptor AgonistsAdenosine A3 Receptor AntagonistsAnimalsDrug Delivery SystemsDrug DesignHumansImmune System DiseasesLigandsReceptor, Adenosine A3Adenosine A3 Receptor AgonistsAdenosine A3 Receptor AntagonistsLigandsReceptor, Adenosine A3

Identifiers

PMID21457061
PMCPMC3613226

What OpenQuestion holds

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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.