Evidence map›Paper›PMID 23535933›Full record

ReviewNature reviews. Drug discovery2013

Adenosine receptors as drug targets--what are the challenges?

Jiang-Fan Chen, Holger K Eltzschig, Bertil B Fredholm

Open access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Drug discovery, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 454 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
454citing papers in PubMed, 1 pooled it
54.2field-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

454 citing papers in PubMed, 1 synthesis or guideline pooled it, 891 citations in OpenAlex.

  1. Pooled it
  2. Neurovascular-immune mediator dynamics in migraine: State-dependent effects of caffeine.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Trial
  3. Pantoprazole as a potential repurposed drug targeting the adenosinergic system in esophageal cancer.Medicinal chemistry research : an international journal for rapid communications on design and mechanisms of action of biologically active agents · 2026
    Article
  4. Review
  5. Article
  6. Review
  7. Adenosine APsychopharmacology · 2026
    Article
  8. Guideline on Stress Echocardiography - 2026.Arquivos brasileiros de cardiologia · 2026
    Article
  9. Article
  10. Article
  11. Discovery of Potent 1,3-Cyclobutane-Containing Dual AACS medicinal chemistry letters · 2026
    Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Adenosine AJournal of neurochemistry · 2026
    Article
  18. Journal of the American Chemical Society · 2026
    Article
  19. Article
  20. Article

394 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

3 authors at 2 institutions in 2 countries.

Jiang-Fan ChenDepartment of Neurology and Pharmacology, Boston University School of Medicine, Boston, Massachusetts 02118, USA.
Holger K Eltzschig
Bertil B Fredholm
Karolinska Institutet · SEUniversity of Colorado Denver · US

Funding

NOVEL BENEFIT OF A2A RECEPTOR INACTIVATION IN PD MODELSR01NS041083 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI CHEN, JIANG-FAN · 2001 to 2013
$3.1M
Extracellular Adenosine During Ventilator Induced Lung InjuryR01HL092188 · NHLBI · UNIVERSITY OF COLORADO DENVER · PI ELTZSCHIG, HOLGER K. · 2009 to 2013
$2.1M
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 R01‑HL0921NHLBI NIH HHS R01 HL092188NHLBI NIH HHS R01 HL098294NHLBI NIH HHS R01‑HL098294NIDDK NIH HHS R01 DK083385NIDDK NIH HHS R01‑DK083385NIDDK NIH HHS R01 DK097075NINDS NIH HHS NS 041083-07NINDS NIH HHS R01 NS041083
6 · The paper itself

Abstract

Adenosine signalling has long been a target for drug development, with adenosine itself or its derivatives being used clinically since the 1940s. In addition, methylxanthines such as caffeine have profound biological effects as antagonists at adenosine receptors. Moreover, drugs such as dipyridamole and methotrexate act by enhancing the activation of adenosine receptors. There is strong evidence that adenosine has a functional role in many diseases, and several pharmacological compounds specifically targeting individual adenosine receptors--either directly or indirectly--have now entered the clinic. However, only one adenosine receptor-specific agent--the adenosine A2A receptor agonist regadenoson (Lexiscan; Astellas Pharma)--has so far gained approval from the US Food and Drug Administration (FDA). Here, we focus on the biology of adenosine signalling to identify hurdles in the development of additional pharmacological compounds targeting adenosine receptors and discuss strategies to overcome these challenges.

Indexed as

Drug DesignMolecular Targeted TherapyAdenosine A2 Receptor AgonistsAnimalsDrug ApprovalHumansPurinesPyrazolesReceptors, Purinergic P1Signal TransductionUnited StatesUnited States Food and Drug AdministrationAdenosine A2 Receptor AgonistsPurinesPyrazolesReceptors, Purinergic P1regadenoson

Identifiers

PMID23535933
PMCPMC3930074
OpenAlexW1975391500

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.