Evidence map›Paper›PMID 25975415›Full record

ReviewJournal of cellular physiology2015

The Many Faces of the A2b Adenosine Receptor in Cardiovascular and Metabolic Diseases.

Anna Eisenstein, Shenia Patterson, Katya Ravid

Abstract readReview
In one paragraph

Review in Journal of cellular physiology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.4field-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

16 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. APurinergic signalling · 2025
    Review
  4. Review
  5. Blockage of the adenosine APurinergic signalling · 2024
    Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Pathological overproduction: the bad side of adenosine.British journal of pharmacology · 2017
    Review
  14. Article
  15. Review
  16. New paradigms in GPCR drug discovery.Biochemical pharmacology · 2015
    Review
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.

Anna EisensteinDepartment of Medicine, Boston University School of Medicine, Boston, Massachusetts.
Shenia PattersonDepartment of Medicine, Boston University School of Medicine, Boston, Massachusetts.
Katya RavidDepartment of Medicine, Boston University School of Medicine, Boston, Massachusetts.
Boston University · US

Funding

Transgenic CoreP30DK046200 · NIDDK · TUFTS MEDICAL CENTER · PI CORKEY, BARBARA E. · 1992 to 2021
$25.0M
Training Program in Cardiovascular Biology: Pre-DoctoralT32HL007969 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAVID, KATYA · 2003 to 2019
$3.2M
Adenosine Receptors and AtherogenesisR01HL093149 · NHLBI · BOSTON UNIVERSITY MEDICAL CAMPUS · PI RAVID, KATYA · 2009 to 2012
$1.6M
A2b Adenosine Receptor Regulation of Metabolic Disease and InflammationF30DK098834 · NIDDK · BOSTON UNIVERSITY MEDICAL CAMPUS · PI EISENSTEIN, ANNA · 2013 to 2015
$126k
NHLBI NIH HHS HL93149NHLBI NIH HHS R01 HL093149NHLBI NIH HHS T32 HL007969NIDDK NIH HHS DK046200NIDDK NIH HHS DK098834NIDDK NIH HHS F30 DK098834NIDDK NIH HHS P30 DK046200
6 · The paper itself

Abstract

Modulation of the low affinity adenosine receptor subtype, the A2b adenosine receptor (A2bAR), has gained interest as a therapeutic target in various pathologic areas associated with cardiovascular disease. The actions of the A2bAR are diverse and at times conflicting depending on cell and tissue type and the timing of activation or inhibition of the receptor. The A2bAR is a promising and exciting pharmacologic target, however, a thorough understanding of A2bAR action is necessary to reach the therapeutic potential of this receptor. This review will focus on the role of the A2bAR in various cardiovascular and metabolic pathologies in which the receptor is currently being studied. We will illustrate the complexities of A2bAR signaling and highlight areas of research with potential for therapeutic development.

Indexed as

Adenosine A2 Receptor AgonistsAdenosine A2 Receptor AntagonistsAnimalsCardiovascular AgentsCardiovascular DiseasesHumansMetabolic DiseasesMolecular Targeted TherapyReceptor, Adenosine A2BSignal TransductionAdenosine A2 Receptor AgonistsAdenosine A2 Receptor AntagonistsCardiovascular AgentsReceptor, Adenosine A2B

Identifiers

PMID25975415
PMCPMC4811601
OpenAlexW2130643872

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.