Evidence map›Paper›PMID 23532575›Full record

ReviewSeminars in thrombosis and hemostasis2013

Plasminogen receptors: the first quarter century.

Lindsey A Miles, Robert J Parmer

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in thrombosis and hemostasis, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 70 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
70citing papers in PubMed, 2 pooled it
4.2field-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

70 citing papers in PubMed, 2 syntheses or guidelines pooled it, 118 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Plg-RMolecular medicine (Cambridge, Mass.) · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Identification of plasminogen-binding sites inFrontiers in cellular and infection microbiology · 2024
    Article
  12. Article
  13. Article
  14. Overexpression of Plg-RAdipocyte · 2023
    Article
  15. Review
  16. Molecular Characterization of the Interplay betweenInternational journal of molecular sciences · 2023
    Article
  17. Article
  18. Review
  19. Article
  20. The Role of Fibrinolytic System in Health and Disease.International journal of molecular sciences · 2022
    Article

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

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 2 institutions in 1 country.

Lindsey A MilesDepartment of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, California 92037, USA. lmiles@scripps.edu
Robert J Parmer
Scripps Research Institute · USVA San Diego Healthcare System · US

Funding

Regulation of plasminogen-dependent cell functions by the novel receptor, Plg-RKTR01HL081046 · NHLBI · SCRIPPS RESEARCH INSTITUTE, THE · PI MILES, LINDSEY A · 2007 to 2024
$8.7M
A Novel Plasminogen Receptor in Breast CancerR01CA166473 · NCI · TORREY PINES INST FOR MOLECULAR STUDIES · PI MILES, LINDSEY A, MUELLER, BARBARA MARIA · 2012 to 2016
$2.1M
PROCESSING OF CHROMOGRANIN A BY THE FIBRINOLYTIC SYSTEMR01HL050398 · NHLBI · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI PARMER, ROBERT J · 1994 to 2001
$424k
Cell Surface Plasminogen Activation and HypertensionI01BX002026 · VA · VA SAN DIEGO HEALTHCARE SYSTEM · PI PARMER, ROBERT J · 2013 to 2016
–
BLRD VA I01 BX002026NCI NIH HHS CA 166473NCI NIH HHS R01 CA166473NHLBI NIH HHS HL 081046NHLBI NIH HHS HL50398NHLBI NIH HHS R01 HL050398NHLBI NIH HHS R01 HL081046
6 · The paper itself

Abstract

The interaction of plasminogen with cell surfaces results in promotion of plasmin formation and retention on the cell surface. This results in arming cell surfaces with the broad-spectrum proteolytic activity of plasmin. Over the past quarter century, key functional consequences of the association of plasmin with the cell surface have been elucidated. Physiologic and pathophysiologic processes with plasmin-dependent cell migration as a central feature include inflammation, wound healing, oncogenesis, metastasis, myogenesis, and muscle regeneration. Cell surface plasmin also participates in neurite outgrowth and prohormone processing. Furthermore, plasmin-induced cell signaling also affects the functions of inflammatory cells, via production of cytokines, reactive oxygen species, and other mediators. Finally, plasminogen receptors regulate fibrinolysis. In this review, we highlight emerging data that shed light on longstanding controversies and raise new issues in the field. We focus on (1) the impact of the recent X-ray crystal structures of plasminogen and the development of antibodies that recognize cell-induced conformational changes in plasminogen on our understanding of the interaction of plasminogen with cells; (2) the relationship between apoptosis and plasminogen binding to cells; (3) the current status of our understanding of the molecular identity of plasminogen receptors and the discovery of a structurally unique novel plasminogen receptor, Plg-RKT; (4) the determinants of the interplay between distinct plasminogen receptors and cellular functions; and (5) new insights into the role of colocalization of plasminogen and plasminogen activator receptors on the cell surface.

Indexed as

Amino Acid SequenceAnimalsCell MembraneFibrinolysinFibrinolysisHumansMolecular Sequence DataPlasminogenPlasminogen ActivatorsReceptors, Cell SurfaceSignal TransductionFibrinolysinPlasminogenPlasminogen ActivatorsReceptors, Cell Surface

Identifiers

PMID23532575
PMCPMC3938387
OpenAlexW2095462890

What Socratic 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 Socratic graph.