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New insights into mineralogenic effects of vanadate

dc.contributor.authorLaizé, Vincent
dc.contributor.authorTiago, Daniel
dc.contributor.authorAureliano, M.
dc.contributor.authorCancela, Leonor
dc.date.accessioned2012-06-28T08:13:08Z
dc.date.available2012-06-28T08:13:08Z
dc.date.issued2009
dc.description.abstractVanadium is a transition metal that occurs naturally in a variety of minerals and exhibits an exceptional complex chemistry in solution, e.g., several oxidation states ranging from ?2 to ?5, and formation of vanadium oligomers such as decameric vanadate (?5) species [1–4]. Besides its metallurgical role in steel alloys, vanadium is also an ultra trace element known to participate in many biological processes and considered to be essential for living organisms [5, 6]. It accumulates in a variety of organisms ranging from microbes to vertebrates, where it modulates the activity of an array of key enzymes or participates as a cofactor in the active centre of others [1, 2, 5–9]. In mammals, vanadium compounds can mimic insulin action and may prevent chemical carcinogenesis, most probably through the inhibition of cellular tyrosine phosphatases and subsequent activation of signalling pathways, suggesting their use as pharmacological tools to treat human diabetes mellitus and cancer, respectively [10–14]. Anti-tumoral action of vanadium is, however, controversial as several studies have proposed that vanadium could act as a mitogen, tumor promoter and co-carcinogen (see [15] and references therein). Other studies have reported an osteogenic role for vanadium compounds and suggest that vanadium could also have a therapeutic application in bone-related diseases, such as osteoporosis [16–18]. Decades of research have thus provided evidence for vanadium’s physiological and pharmacological properties, supporting the claim that it may represent a promising therapeutic agent for diseases targeting billions of human beings and affecting a wide range of pathological conditions. However, the development of vanadium-based pharmaceuticals will probably take some time since various issues related to vanadium toxicity, speciation and multiple targeting will need to be solved before advancing to clinical trials. Despite being used for decades by researchers as an inhibitor of protein tyrosine phosphatases, it is still not totally clear which vanadium species induce or which signalling pathways transduce physiological and pharmacological effects. Vanadium chemistry is complex, and different species or complexes may induce different pathways [5], affecting different biological processes. This work intends to review what is presently known about the bone-related role of vanadium in mammals and present recent in vitro data on the mineralogenic effect of vanadate in fish, which have become promising model organisms for vertebrate bone-related studies.por
dc.identifier.issn1420-682X
dc.identifier.urihttp://hdl.handle.net/10400.1/1360
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherSpringerpor
dc.subjectVanadatepor
dc.subjectBone mineralizationpor
dc.titleNew insights into mineralogenic effects of vanadatepor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage3836por
oaire.citation.issue66por
oaire.citation.startPage3831por
oaire.citation.titleCellular and Molecular Life Sciencespor
person.familyNameLaizé
person.familyNameTiago
person.familyNameAureliano
person.familyNameCancela
person.givenNameVincent
person.givenNameDaniel
person.givenNameManuel
person.givenNameM. Leonor
person.identifier584146
person.identifier.ciencia-idAA14-3490-DC5E
person.identifier.orcid0000-0001-9565-9198
person.identifier.orcid0000-0001-8418-6292
person.identifier.orcid0000-0003-4858-3201
person.identifier.orcid0000-0003-3114-6662
person.identifier.ridB-4463-2008
person.identifier.ridI-3283-2012
person.identifier.scopus-author-id6602982778
person.identifier.scopus-author-id14422711000
person.identifier.scopus-author-id6603412860
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor
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relation.isAuthorOfPublicationbb413661-7edd-4b57-8338-33889cfd05db
relation.isAuthorOfPublicationb9bbfe32-3dfe-4131-ad14-a4394008447f
relation.isAuthorOfPublication.latestForDiscovery10cda3a0-7b9c-4d16-bd2a-a06df1d56d94

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