Evidence map›Paper›PMID 35008762›Full record

ReviewInternational journal of molecular sciences2021

The Plasminogen-Activator Plasmin System in Physiological and Pathophysiological Angiogenesis.

Asmaa Anwar Ismail, Baraah Tariq Shaker, Khalid Bajou

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed, 1 pooled it
6.6field-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

85 citing papers in PubMed, 1 synthesis or guideline pooled it, 116 citations in OpenAlex.

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25 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

3 authors at 1 institution in 1 country.

Asmaa Anwar IsmailDepartment of Applied Biology, College of Sciences, University of Sharjah, Sharjah 27272, United Arab Emirates.ORCID 0000-0002-6672-4533
Baraah Tariq ShakerDepartment of Applied Biology, College of Sciences, University of Sharjah, Sharjah 27272, United Arab Emirates.
Khalid BajouDepartment of Applied Biology, College of Sciences, University of Sharjah, Sharjah 27272, United Arab Emirates.
University of Sharjah · AE

Funding

Competitive Research grant, university of Sharjah V.C.R.G./R.824/2018
6 · The paper itself

Abstract

Angiogenesis is a process associated with the migration and proliferation of endothelial cells (EC) to form new blood vessels. It is involved in various physiological and pathophysiological conditions and is controlled by a wide range of proangiogenic and antiangiogenic molecules. The plasminogen activator-plasmin system plays a major role in the extracellular matrix remodeling process necessary for angiogenesis. Urokinase/tissue-type plasminogen activators (uPA/tPA) convert plasminogen into the active enzyme plasmin, which in turn activates matrix metalloproteinases and degrades the extracellular matrix releasing growth factors and proangiogenic molecules such as the vascular endothelial growth factor (VEGF-A). The plasminogen activator inhibitor-1 (PAI-1) is the main inhibitor of uPA and tPA, thereby an inhibitor of pericellular proteolysis and intravascular fibrinolysis, respectively. Paradoxically, PAI-1, which is expressed by EC during angiogenesis, is elevated in several cancers and is found to promote angiogenesis by regulating plasmin-mediated proteolysis and by promoting cellular migration through vitronectin. The urokinase-type plasminogen activator receptor (uPAR) also induces EC cellular migration during angiogenesis via interacting with signaling partners. Understanding the molecular functions of the plasminogen activator plasmin system and targeting angiogenesis via blocking serine proteases or their interactions with other molecules is one of the major therapeutic strategies scientists have been attracted to in controlling tumor growth and other pathological conditions characterized by neovascularization.

Indexed as

Neovascularization, PhysiologicAnimalsHumansModels, BiologicalNeovascularization, PathologicPlasminogenSerine ProteasesTissue Plasminogen ActivatorPlasminogenSerine ProteasesTissue Plasminogen Activatorangiogenesisendothelial cellsplasminplasminogen-activator inhibitor-1 (PAI-1)urokinase-plasminogen activator (uPA)vascular endothelial growth factor (VEGF)

Identifiers

PMID35008762
PMCPMC8745544
OpenAlexW4200271992

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.