<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-27T05:36:32Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/14679" metadataPrefix="mods">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/14679</identifier><datestamp>2026-02-03T10:58:10Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</setSpec></header><metadata><mods:mods xmlns:doc="http://www.lyncode.com/xoai" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-1.xsd">
   <mods:name>
      <mods:namePart>García-Caballero, Melissa</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Blacher, S.</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Pauper, J.</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Rodríguez-Quesada, Ana María</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Medina-Torres, Miguel Ángel</mods:namePart>
   </mods:name>
   <mods:name>
      <mods:namePart>Noël, Agnès</mods:namePart>
   </mods:name>
   <mods:extension>
      <mods:dateAvailable encoding="iso8601">2017-10-23T07:37:04Z</mods:dateAvailable>
   </mods:extension>
   <mods:extension>
      <mods:dateAccessioned encoding="iso8601">2017-10-23T07:37:04Z</mods:dateAccessioned>
   </mods:extension>
   <mods:originInfo>
      <mods:dateIssued encoding="iso8601">2016</mods:dateIssued>
   </mods:originInfo>
   <mods:identifier type="citation">Br. J. Pharmacol. 173, 1966-1987, 2016</mods:identifier>
   <mods:identifier type="uri">http://hdl.handle.net/10630/14679</mods:identifier>
   <mods:identifier type="doi">10.1111/bph.13488</mods:identifier>
   <mods:abstract>BACKGROUND AND PURPOSE&#xd;
Lymphangiogenesis is an important biological process associated with the pathogenesis of several diseases, including metastatic&#xd;
dissemination, graft rejection, lymphoedema and other inflammatory disorders. The development of new drugs that block&#xd;
lymphangiogenesis has become a promising therapeutic strategy. In this study, we investigated the ability of toluquinol,&#xd;
a 2-methyl-hydroquinone isolated from the culture broth of the marine fungus Penicillium sp. HL-85-ALS5-R004, to inhibit&#xd;
lymphangiogenesis in vitro, ex vivo and in vivo.&#xd;
EXPERIMENTAL APPROACH&#xd;
We used human lymphatic endothelial cells (LECs) to analyse the effect of toluquinol in 2D and 3D in vitro cultures and in the&#xd;
ex vivo mouse lymphatic ring assay. For in vivo approaches, the transgenic Fli1:eGFPy1 zebrafish, mouse ear sponges and cornea&#xd;
models were used. Western blotting and apoptosis analyses were carried out to search for drug targets.&#xd;
KEY RESULTS&#xd;
Toluquinol inhibited LEC proliferation,migration, tubulogenesis and sprouting of new lymphatic vessels. Furthermore, toluquinol&#xd;
induced apoptosis of LECs after 14 h of treatment in vitro, blocked the development of the thoracic duct in zebrafish and reduced&#xd;
the VEGF-C-induced lymphatic vessel formation and corneal neovascularization in mice. Mechanistically, we demonstrated that&#xd;
this drug attenuates VEGF-C-induced VEGFR-3 phosphorylation in a dose-dependentmanner and suppresses the phosphorylation&#xd;
of Akt and ERK1/2.&#xd;
CONCLUSIONS AND IMPLICATIONS&#xd;
Based on these findings, we propose toluquinol as a new candidate with pharmacological potential for the treatment of&#xd;
lymphangiogenesis-related pathologies. Notably, its ability to suppress corneal neovascularization paves the way for applications&#xd;
in vascular ocular pathologies.</mods:abstract>
   <mods:language>
      <mods:languageTerm>spa</mods:languageTerm>
   </mods:language>
   <mods:accessCondition type="useAndReproduction">open access</mods:accessCondition>
   <mods:accessCondition type="useAndReproduction">by-nc-nd</mods:accessCondition>
   <mods:subject>
      <mods:topic>Antiangiogénicos</mods:topic>
   </mods:subject>
   <mods:titleInfo>
      <mods:title>Novel application assigned to toluquinol: inhibition of lymphangiogenesis by interfering with VEGF-C/VEGFR-3 signalling pathway</mods:title>
   </mods:titleInfo>
   <mods:genre>journal article</mods:genre>
</mods:mods>
</metadata></record></GetRecord></OAI-PMH>