Evidence map›Paper›PMID 28688145›Full record

ArticleBritish journal of pharmacology2017

Therapeutic concentrations of digitoxin inhibit endothelial focal adhesion kinase and angiogenesis induced by different growth factors.

Annalisa Trenti, Elisabetta Zulato, Lorenza Pasqualini, Stefano Indraccolo, Chiara Bolego, Lucia Trevisi

Open access · bronzeAbstract read
In one paragraph

Article in British journal of pharmacology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
3.3field-weighted citation impact, top 7% 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

24 citing papers in PubMed, 44 citations in OpenAlex.

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  9. NaMolecules (Basel, Switzerland) · 2021
    Review
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  13. Cardenolide-rich fraction of Pergularia tomentosa as a novel Antiangiogenic agent mainly targeting endothelial cell migration.Daru : journal of Faculty of Pharmacy, Tehran University of Medical Sciences · 2020
    Article
  14. Article
  15. Naturally Occurring Cardenolides AffectingACS infectious diseases · 2020
    Article
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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

6 authors at 2 institutions in 1 country.

Annalisa TrentiDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy.
Elisabetta ZulatoIstituto Oncologico Veneto IOV - IRCCS, Padova, Italy.
Lorenza PasqualiniIstituto Oncologico Veneto IOV - IRCCS, Padova, Italy.
Stefano IndraccoloIstituto Oncologico Veneto IOV - IRCCS, Padova, Italy.
Chiara BolegoDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy.
Lucia TrevisiDepartment of Pharmaceutical and Pharmacological Sciences, University of Padova, Padova, Italy.ORCID http://orcid.org/0000-0001-5008-9240
Istituto Oncologico Veneto · ITUniversity of Padua · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeCardiac glycosides are Na EXPERIMENTAL APPROACH: We studied the effect of digoxin, digitoxin and ouabain on early events of the angiogenic process in HUVECs. We determined HUVEC viability, proliferation, migration and differentiation into capillary tube-like structures. We also tested drug activity using an in vivo angiogenesis model. Activation of protein tyrosine kinase 2 (FAK) and signalling proteins associated with the Na KEY

resultsDigitoxin and ouabain (1-100 nM) inhibited HUVEC migration, concentration-dependently, without affecting cell viability, while digoxin induced apoptosis at the same concentrations. Digitoxin antagonized growth factor-induced migration and tubularization at concentrations (1-25 nM) within its plasma therapeutic range. The anti-angiogenic effect of digitoxin was confirmed also by in vivo studies. Digitoxin induced Src, Akt and ERK1/2 phosphorylation but did not affect FAK autophosphorylation at Tyr CONCLUSIONS AND IMPLICATIONS: Therapeutic concentrations of digitoxin inhibited angiogenesis and FAK activation by several pro-angiogenic stimuli. These novel findings suggest a potential repositioning of digitoxin as a broad-spectrum anti-angiogenic drug for diseases where pathological angiogenesis is involved.

Indexed as

Angiogenesis InhibitorsApoptosisCell DifferentiationCell MovementCell ProliferationCell SurvivalDigitoxinDose-Response Relationship, DrugFocal Adhesion Protein-Tyrosine KinasesHumansHuman Umbilical Vein Endothelial CellsIntercellular Signaling Peptides and ProteinsNeovascularization, PathologicProtein Kinase InhibitorsStructure-Activity RelationshipAngiogenesis InhibitorsDigitoxinFocal Adhesion Protein-Tyrosine KinasesIntercellular Signaling Peptides and ProteinsProtein Kinase Inhibitors

Identifiers

PMID28688145
PMCPMC5573418
OpenAlexW2735251791

What OpenQuestion holds

Textmetadata
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.