Evidence map›Paper›PMID 26694425›Full record

ArticleMarine drugs2015

Low-Molecular-Weight Fucoidan Induces Endothelial Cell Migration via the PI3K/AKT Pathway and Modulates the Transcription of Genes Involved in Angiogenesis.

Claire Bouvard, Isabelle Galy-Fauroux, Françoise Grelac, Wassila Carpentier, Anna Lokajczyk, Sophie Gandrille, Sylvia Colliec-Jouault, Anne-Marie Fischer, Dominique Helley

Open access · goldAbstract read
In one paragraph

Article in Marine drugs, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
5.7field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 41 citations in OpenAlex.

  1. Targeting Signalling Pathways in Chronic Wound Healing.International journal of molecular sciences · 2023
    Review
  2. Article
  3. Comparison of Fucoidans fromInternational journal of molecular sciences · 2023
    Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Fucoidans in Nanomedicine.Marine drugs · 2016
    Review
  16. Erythropoietin Pathway: A Potential Target for the Treatment of Depression.International journal of molecular sciences · 2016
    Review
  17. 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

9 authors at 3 institutions in 1 country.

Claire BouvardInserm, UMR-S765, 75006 Paris, France. bouvard.claire@gmail.com.
Isabelle Galy-FaurouxUniversité Paris Descartes, Sorbonne Paris Cité, 75006 Paris, France. isabelle.galy-fauroux@parisdescartes.fr.
Françoise GrelacInserm, UMR-S765, 75006 Paris, France. francoise.grelac@parisdescartes.fr.
Wassila CarpentierPlateforme P3S, Sorbonne Universités, 75013 Paris, France. wassila.carpentier@upmc.fr.
Anna LokajczykUniversité Paris Descartes, Sorbonne Paris Cité, 75006 Paris, France. anna.lokajczyk@parisdescartes.fr.
Sophie GandrilleUniversité Paris Descartes, Sorbonne Paris Cité, 75006 Paris, France. sophie.gandrille@parisdescartes.fr.
Sylvia Colliec-JouaultIFREMER, Route de l'Ile d'Yeu, 44300 Nantes, France. sylvia.colliec.jouault@ifremer.fr.
Anne-Marie FischerUniversité Paris Descartes, Sorbonne Paris Cité, 75006 Paris, France. anne-marie.fischer@egp.aphp.fr.
Dominique HelleyUniversité Paris Descartes, Sorbonne Paris Cité, 75006 Paris, France. dominique.helley@egp.aphp.fr.
Délégation Paris 5 · FRIfremer · FRSorbonne Université · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Low-molecular-weight fucoidan (LMWF) is a sulfated polysaccharide extracted from brown seaweed that presents antithrombotic and pro-angiogenic properties. However, its mechanism of action is not well-characterized. Here, we studied the effects of LMWF on cell signaling and whole genome expression in human umbilical vein endothelial cells and endothelial colony forming cells. We observed that LMWF and vascular endothelial growth factor had synergistic effects on cell signaling, and more interestingly that LMWF by itself, in the absence of other growth factors, was able to trigger the activation of the PI3K/AKT pathway, which plays a crucial role in angiogenesis and vasculogenesis. We also observed that the effects of LMWF on cell migration were PI3K/AKT-dependent and that LMWF modulated the expression of genes involved at different levels of the neovessel formation process, such as cell migration and cytoskeleton organization, cell mobilization and homing. This provides a better understanding of LMWF's mechanism of action and confirms that it could be an interesting therapeutic approach for vascular repair.

Indexed as

Cell MovementCytoskeletonGene Expression RegulationHumansHuman Umbilical Vein Endothelial CellsMolecular WeightNeovascularization, PhysiologicPhosphatidylinositol 3-KinasePolysaccharidesProto-Oncogene Proteins c-aktVascular Endothelial Growth Factor AfucoidanPhosphatidylinositol 3-KinasePolysaccharidesProto-Oncogene Proteins c-aktVascular Endothelial Growth Factor Aangiogenesisfucoidanmigrationsignalingtranscriptomicsvasculogenesis

Identifiers

PMID26694425
PMCPMC4699248
OpenAlexW2213344075

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.