Evidence map›Paper›PMID 21838667›Full record

ReviewCardiovascular & hematological agents in medicinal chemistry2011

12-lipoxygenase: a potential target for novel anti-platelet therapeutics.

Jennifer Yeung, Michael Holinstat

Open access · bronzeAbstract readReview
In one paragraph

Review in Cardiovascular & hematological agents in medicinal chemistry, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

41 citing papers in PubMed, 71 citations in OpenAlex.

  1. Trial
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Antiplatelet strategies: past, present, and future.Journal of thrombosis and haemostasis : JTH · 2023
    Review
  8. Article
  9. Review
  10. Article
  11. ML355 Modulates Platelet Activation and Prevents ABT-737 Induced Apoptosis in Platelets.The Journal of pharmacology and experimental therapeutics · 2022
    Article
  12. Antioxidants (Basel, Switzerland) · 2022
    Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Article
  20. Article
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

2 authors at 1 institution in 1 country.

Jennifer YeungDepartment of Medicine, Cardeza Foundation for Hematologic Research, Thomas Jefferson University, Philadelphia, PA, USA.
Michael Holinstat
Thomas Jefferson University · US

Funding

Thrombin regulation of Rap1 signaling in human platelet activityR00HL089457 · NHLBI · THOMAS JEFFERSON UNIVERSITY · PI HOLINSTAT, MICHAEL ALLAN · 2008 to 2010
$747k
Thrombin regulation of Rap1 signaling in human platelet activityK99HL089457 · NHLBI · VANDERBILT UNIVERSITY · PI HOLINSTAT, MICHAEL ALLAN · 2007 to 2008
$180k
NHLBI NIH HHS HL089457NHLBI NIH HHS K99 HL089457NHLBI NIH HHS R00 HL089457
6 · The paper itself

Abstract

Platelets play an essential role in the regulation of hemostasis and thrombosis and controlling their level of activation is central to prevention of occlusive clot formation and stroke. Although a number of anti-platelet targets have been identified to address this issue including COX-1, the P2Y(12) receptor, the integrin αIIbβ3, and more recently the protease-activated receptor-1, these targets often result in a significant increased risk of bleeding which may lead to pathologies as serious as the thrombosis they were meant to treat including intracranial hemorrhage and gastrointestinal bleeding. Therefore, alternative approaches to treat uncontrolled platelet activation are warranted. Platelet-type 12-lipoxygenase is an enzyme which oxidizes the free fatty acid in the platelet resulting in the production of the stable metabolite 12-hydroxyeicosatetraenoic acid (12-HETE). The role of 12-HETE in the platelet has been controversial with reports associating its function as being both anti- and pro-thrombotic. In this review, the role of 12-lipoxygenase and its bioactive metabolites in regulation of platelet reactivity, clot formation, and hemostasis is described. Understanding the mechanisms by which 12-lipoxygenase and its metabolites modulate platelet function may lead to the development of a novel class of anti-platelet therapies targeting the enzyme in order to attenuate injury-induced clot formation, vessel occlusion and pathophysiological shifts in hemostasis.

Indexed as

AnimalsArachidonate 12-LipoxygenaseBlood PlateletsHemostasisHumansLipoxygenase InhibitorsPlatelet Aggregation InhibitorsThrombosisArachidonate 12-LipoxygenaseLipoxygenase InhibitorsPlatelet Aggregation Inhibitors

Identifiers

PMID21838667
PMCPMC3171607
OpenAlexW2039387432

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.