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PTEN “meets” DMSO

dc.contributor.authorSantos, Nuno C.
dc.contributor.authorMartins e Silva, João
dc.contributor.authorSaldanha, Carlota
dc.date.accessioned2020-10-23T13:21:59Z
dc.date.available2020-10-23T13:21:59Z
dc.date.issued2005
dc.description© 2004 Elsevier Ltd. All rights reserved.pt_PT
dc.description.abstractThe PTEN proteins (PTEN, for phosphatase and tensin homolog deleted on chromosome ten) are a family of multi-specific phosphatases able to use both lipidic and proteic substrates (for recent reviews on their biochemistry and biomedical relevance see, e.g. The most important physiological PTEN substrate is the lipidic second messenger phosphatidylinositol-3,4,5-trisphosphate (PIP3). Thus, PTEN reverts the phosphoinositide-3-kinases (PI3K) phosphorilation of phosphatidylinositol-4,5-bisphosphate (PIP2) to PIP3. As PIP3 activates the serine–threonine kinase Akt, which is involved in anti-apoptosis, proliferation and oncogenesis, its dephosphorylation by PTEN negatively regulates tumorigenesis. Mutations in the PTEN gene in human can lead to sporadic cancers (e.g., glioblastoma, endometrial and prostatic cancers) or to hereditary disorders characterized by multiple hamartomas and increased risk of cancers (Cowden disease, Bannayan-Zonana syndrome and Lhermitte-Duclos disease). PTEN expression is also associated with neuronal differentiation, and G1 phase cell cycle arrest in cell cultures.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationLeukemia Research, Vol. 29, Issue 4, 2005, pp. 361-362pt_PT
dc.identifier.doi10.1016/j.leukres.2004.09.009pt_PT
dc.identifier.issn0145-2126
dc.identifier.urihttp://hdl.handle.net/10451/44650
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.relation.publisherversionhttps://www.sciencedirect.com/journal/leukemia-researchpt_PT
dc.titlePTEN “meets” DMSOpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage362pt_PT
oaire.citation.issue4pt_PT
oaire.citation.startPage361pt_PT
oaire.citation.titleLeukemia Researchpt_PT
oaire.citation.volume29pt_PT
person.familyNameSantos
person.familyNameSaldanha
person.givenNameNuno
person.givenNameCarlota
person.identifier53901
person.identifier.ciencia-idCD13-5E3A-A3C5
person.identifier.orcid0000-0002-0580-0475
person.identifier.orcid0000-0002-5058-2112
person.identifier.ridN-7248-2013
person.identifier.scopus-author-id55940818300
rcaap.rightsrestrictedAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication4656d912-5a2d-4c80-8921-2bcba3aa441a
relation.isAuthorOfPublicationad6de30c-87ca-4613-bb87-488dd5d285d0
relation.isAuthorOfPublication.latestForDiscovery4656d912-5a2d-4c80-8921-2bcba3aa441a

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