Evidence map›Paper›PMID 24845219›Full record

ReviewCurrent drug targets2014

The role of P2Y₁₂ receptor and activated platelets during inflammation.

Elisabetta Liverani, Laurie E Kilpatrick, Alexander Y Tsygankov, Satya P Kunapuli

Abstract readReview
In one paragraph

Review in Current drug targets, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 57 citations in OpenAlex.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Platelet P2YBritish journal of pharmacology · 2024
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Pleiotropic Effects of Ticagrelor: Influence onDrug design, development and therapy · 2022
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Microglia and Neuroinflammation: What Place for P2RY12?International journal of molecular sciences · 2021
    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

4 authors at 1 institution in 1 country.

Elisabetta Liverani
Laurie E Kilpatrick
Alexander Y Tsygankov
Satya P KunapuliSol Scherry Thrombosis Research Center 3420 N. Brad Street, Philadelphia 19140, USA. eliliverani@temple.edu.
Temple University · US

Funding

Functional PKC Isoforms in PlateletsR01HL093231 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KUNAPULI, SATYA P. · 2009 to 2017
$3.6M
Regulation and function of PDK1-Akt-Pyk2 axis in plateletsR01HL118593 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KUNAPULI, SATYA P. · 2013 to 2016
$1.9M
Novel Protein Kinase C Targeted Therapy for Acute Lung InjuryR01HL111552 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI KILPATRICK, LAURIE E · 2012 to 2015
$1.5M
NHLBI NIH HHS HL118593NHLBI NIH HHS HL93231NHLBI NIH HHS R01 HL093231NHLBI NIH HHS R01 HL111552NHLBI NIH HHS R01 HL118593
6 · The paper itself

Abstract

Platelets play an important role not only during thrombosis, but also in modulating immune responses through their interaction with immune cells and by releasing inflammatory mediators upon activation. The P2Y12 receptor is a Gi-coupled receptor that not only regulates ADP-induced aggregation but can also dramatically potentiate secretion, when platelets are activated by other stimuli. Considering the importance of P2Y12 receptor in platelet function, a class of antiplatelet drugs, thienopyridines, have been designed and successfully used to prevent thrombosis. This review will focus on the role of activated platelets in inflammation and the effects that P2Y12 antagonism exerts on the inflammatory process. A change in platelet functions was noted in patients treated with thienopyridines during inflammatory conditions, suggesting that platelets may modulate the inflammatory response. Further experiments in a variety of animal models of diseases, such as sepsis, rheumatoid arthritis, myocardial infarction, pancreatitis and pulmonary inflammation have also demonstrated that activated platelets influence the inflammatory state. Platelets can secrete inflammatory modulators in a P2Y12-dependent manner, and, as a result, directly alter the inflammatory response. P2Y12 receptor may also be expressed in other cells of the immune system, indicating that thienopyridines could directly influence the immune system rather than only through platelets. Overall the results obtained to date strongly support the notion that activated platelets significantly contribute to the inflammatory process and that antagonizing P2Y12 receptor can influence the immune response.

Indexed as

AnimalsBlood PlateletsDisease Models, AnimalHumansInflammationInflammation MediatorsPlatelet ActivationPurinergic P2Y Receptor AntagonistsReceptors, Purinergic P2Y12ThienopyridinesInflammation MediatorsPurinergic P2Y Receptor AntagonistsReceptors, Purinergic P2Y12Thienopyridines

Identifiers

PMID24845219
PMCPMC5681251
OpenAlexW2128528190

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.