Evidence map›Paper›PMID 24589267›Full record

ReviewHematology/oncology clinics of North America2014

The role of adenosine signaling in sickle cell therapeutics.

Joshua J Field, David G Nathan, Joel Linden

Erratum issuedAbstract readReview
In one paragraph

Review in Hematology/oncology clinics of North America, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.5field-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

12 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. New Therapeutic Options for the Treatment of Sickle Cell Disease.Mediterranean journal of hematology and infectious diseases · 2019
    Review
  5. Review
  6. Inflammation in sickle cell disease.Clinical hemorheology and microcirculation · 2018
    Article
  7. Article
  8. Red cell DAMPs and inflammation.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2016
    Review
  9. Inflammatory targets of therapy in sickle cell disease.Translational research : the journal of laboratory and clinical medicine · 2016
    Review
  10. Review
  11. Review
  12. Article
4 · The record

Corrections and comments

  • Erratum issued
5 · Who and what money

Authors and funding

3 authors at 3 institutions in 1 country.

Joshua J FieldBlood Research Institute, BloodCenter of Wisconsin, 8733 Watertown Plank Road, Milwaukee, WI 53226, USA; Department of Medicine, Medical College of Wisconsin, 9200 West Wisconsin Avenue, Milwaukee, WI 53226, USA. Electronic address: joshua.field@bcw.edu.
David G NathanDepartment of Pediatric Oncology, Dana-Farber Cancer Institute, 450 Brookline Avenue, Boston, MA 02215, USA; Division of Pediatric Hematology and Oncology, Boston Children's Hospital, 300 Longwood Avenue, Boston, MA 02115, USA; Department of Pediatrics, Harvard Medical School, 25 Shattuck Street, Boston, MA 02115, USA.
Joel LindenInflammation Biology, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, San Diego, CA 92037, USA.
Harvard University · USLa Jolla Institute for Immunology · USVersiti Blood Center of Wisconsin · US

Funding

A Controlled Clinical Trial of Regadenoson in Sickle Cell AnemiaP50HL110790 · NHLBI · DANA-FARBER CANCER INST · PI FIELD, JOSHUA JEFFREY, LINDEN, JOEL M. · 2012 to 2016
$10.8M
Targeted CEU Imaging of Atherosclerosis and AngiogenesisR01HL078610 · NHLBI · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI LINDNER, JONATHAN R · 2004 to 2022
$6.8M
Biomarkers of Inflammation and Vaso-occlusion in Sickle Cell DiseaseR01HL111969 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI FIELD, JOSHUA JEFFREY, LINDEN, JOEL M. · 2012 to 2016
$4.0M
Lymphocyte Activation in Sickle Cell Lung DiseaseR01HL095704 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI LINDEN, JOEL M. · 2010 to 2014
$2.3M
CTRIP: Treatment of Sickle Cell Crisis with inhibitors of NKT cell activationRC2HL101367 · NHLBI · DANA-FARBER CANCER INST · PI LINDEN, JOEL M., NATHAN, DAVID G. · 2009 to 2010
$1.8M
A Feasibility Study of Regadenoson for the Treatment of Acute Chest SyndromeR34HL108757 · NHLBI · DANA-FARBER CANCER INST · PI FIELD, JOSHUA JEFFREY, NATHAN, DAVID G. · 2011 to 2012
$682k
NHLBI NIH HHS P50 HL110790NHLBI NIH HHS R01 HL078610NHLBI NIH HHS R01 HL095704NHLBI NIH HHS R01 HL111969NHLBI NIH HHS R34 HL108757NHLBI NIH HHS RC2 HL101367
6 · The paper itself

Abstract

Data suggest a role for adenosine signaling in the pathogenesis of sickle cell disease (SCD). Signaling through the adenosine A2A receptor (A2AR) has demonstrated beneficial effects. Activation of A2ARs decreases inflammation with SCD by blocking activation of invariant natural killer T cells. Decreased inflammation may reduce the severity of vasoocclusive crises. Adenosine signaling through the adenosine A2B receptor (A2BR) may be detrimental in SCD. Whether adenosine signaling predominantly occurs through A2ARs or A2BRs may depend on differing levels of adenosine and disease state (steady state versus crisis). There may be opportunities to develop novel therapeutic approaches targeting A2ARs and/or A2BRs for patients with SCD.

Indexed as

Adenosine A2 Receptor AgonistsAdenosine A2 Receptor AntagonistsAnemia, Sickle CellAnimalsHumansPurinesPyrazolesReceptor, Adenosine A2AReceptor, Adenosine A2BSignal TransductionAdenosine A2 Receptor AgonistsAdenosine A2 Receptor AntagonistsN-(4-acetylphenyl)-2-(4-(2,3,6,7-tetrahydro-2,6-dioxo-1,3-dipropyl-1H-purin-8-yl)phenoxy)acetamidePurinesPyrazolesReceptor, Adenosine A2AReceptor, Adenosine A2BregadenosonAdenosineAdenosine A(2A) receptorAdenosine A(2B) receptorNKT cellsSickle cell disease

Identifiers

PMID24589267
PMCPMC3997263
OpenAlexW1999948518

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.