Evidence map›Paper›PMID 25256236›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2015

Targeting integrin and integrin signaling in treating thrombosis.

Brian Estevez, Bo Shen, Xiaoping Du

Erratum issuedOpen access · bronzeAbstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2015. 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 66 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 2% 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

66 citing papers in PubMed, 1 synthesis or guideline pooled it, 130 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Review
  9. Review
  10. Integrins as Drug Targets in Vascular and Related Diseases.International journal of drug discovery and pharmacology · 2024
    Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Targeting integrin pathways: mechanisms and advances in therapy.Signal transduction and targeted therapy · 2023
    Review
  18. Article
  19. Review
  20. Review

6 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

Brian EstevezFrom the Department of Pharmacology, University of Illinois at Chicago.
Bo ShenFrom the Department of Pharmacology, University of Illinois at Chicago.
Xiaoping DuFrom the Department of Pharmacology, University of Illinois at Chicago. xdu@uic.edu.
University of Illinois Chicago · US

Funding

Signaling mechanisms of platelet GPIb-IXR01HL062350 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DU, XIAOPING · 2000 to 2017
$6.0M
Outside-in signaling mechanisms of platelet integrin alpha-llb-beta3R01HL080264 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI DU, XIAOPING · 2007 to 2019
$4.6M
Investigation into the mechanism of the thrombin receptor function of GPIBF31HL123319 · NHLBI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ESTEVEZ, BRIAN · 2014 to 2015
$86k
NHLBI NIH HHS F31 HL123319NHLBI NIH HHS HHSN268201400007CNHLBI NIH HHS HL062350NHLBI NIH HHS HL080264NHLBI NIH HHS R01 HL062350NHLBI NIH HHS R01 HL080264
6 · The paper itself

Abstract

The critical roles of integrins in thrombosis have enabled the successful development and clinical use of the first generation of integrin antagonists as represented by abciximab (Reopro), eptifibatide (Integrilin), and tirofiban (Aggrastat). These integrin αIIbβ3 antagonists are not only potent antithrombotics but also have significant side effects. In particular, their induction of ligand-induced integrin conformational changes is associated with thrombocytopenia. Increased bleeding risk prevents integrin antagonists from being used at higher doses and in patients at risk for bleeding. To address the ligand-induced conformational changes caused by current integrin antagonists, compounds that minimally induce conformational changes in integrin αIIbβ3 have been developed. Recent studies on the mechanisms of integrin signaling suggest that selectively targeting integrin outside-in signaling mechanisms allows for potent inhibition of thrombosis, while maintaining hemostasis in animal models.

Indexed as

Molecular Targeted TherapyAnimalsBlood PlateletsDrug DesignFibrinolytic AgentsHemorrhageHumansIntegrinsLigandsProtein ConformationRisk FactorsSignal TransductionThrombocytopeniaThrombosisFibrinolytic AgentsIntegrinsLigandsblood plateletsintegrinsplatelet aggregation inhibitorsthrombosis

Identifiers

PMID25256236
PMCPMC4270936
OpenAlexW2146521009

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.