Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/108280
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dc.contributor.authorSorrentino, Giovanni-
dc.contributor.authorRuggeri, Naomi-
dc.contributor.authorZannini, Alessandro-
dc.contributor.authorIngallina, Eleonora-
dc.contributor.authorBertolio, Rebecca-
dc.contributor.authorMarotta, Carolina-
dc.contributor.authorNeri, Carmelo-
dc.contributor.authorCappuzzello, Elisa-
dc.contributor.authorForcato, Mattia-
dc.contributor.authorRosato, Antonio-
dc.contributor.authorMano, Miguel-
dc.contributor.authorBicciato, Silvio-
dc.contributor.authorDel Sal, Giannino-
dc.date.accessioned2023-08-22T10:52:28Z-
dc.date.available2023-08-22T10:52:28Z-
dc.date.issued2017-01-19-
dc.identifier.issn2041-1723pt
dc.identifier.urihttps://hdl.handle.net/10316/108280-
dc.description.abstractThe Hippo pathway is an oncosuppressor signalling cascade that plays a major role in the control of cell growth, tissue homoeostasis and organ size. Dysregulation of the Hippo pathway leads to aberrant activation of the transcription co-activator YAP (Yes-associated protein) that contributes to tumorigenesis in several tissues. Here we identify glucocorticoids (GCs) as hormonal activators of YAP. Stimulation of glucocorticoid receptor (GR) leads to increase of YAP protein levels, nuclear accumulation and transcriptional activity in vitro and in vivo. Mechanistically, we find that GCs increase expression and deposition of fibronectin leading to the focal adhesion-Src pathway stimulation, cytoskeleton-dependent YAP activation and expansion of chemoresistant cancer stem cells. GR activation correlates with YAP activity in human breast cancer and predicts bad prognosis in the basal-like subtype. Our results unveil a novel mechanism of YAP activation in cancer and open the possibility to target GR to prevent cancer stem cells self-renewal and chemoresistance.pt
dc.language.isoengpt
dc.relationgrants from the Associazione Italiana per la Ricerca sul Cancro (AIRC) and AIRC Special Program Molecular Clinical Oncology ‘5 per mille’ (Grant no. 10016) and Italian Ministry of Health, to G.D.S.,S.B. and A.R.pt
dc.relationM.M. is supported by the FIRB RBAP11Z4Z9 project from the Italian Ministry of Education and the FCT Investigator Programme IF/00694/2013 from the Portuguese Foundation for Science and Technology (FCT), Portugalpt
dc.relationM.F. is supported by FIRB RBAP11T3WB and ERC grant no. 670126 Denovostem.pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt
dc.subject.meshAdaptor Proteins, Signal Transducingpt
dc.subject.meshAnimalspt
dc.subject.meshBreast Neoplasmspt
dc.subject.meshCell Line, Tumorpt
dc.subject.meshFemalept
dc.subject.meshGene Expression Regulation, Neoplasticpt
dc.subject.meshGlucocorticoidspt
dc.subject.meshHumanspt
dc.subject.meshMicept
dc.subject.meshMice, Inbred C57BLpt
dc.subject.meshNeoplasms, Experimentalpt
dc.subject.meshPhosphoproteinspt
dc.subject.meshReceptors, Glucocorticoidpt
dc.subject.meshSignal Transductionpt
dc.subject.meshTranscription Factorspt
dc.subject.meshYAP-Signaling Proteinspt
dc.titleGlucocorticoid receptor signalling activates YAP in breast cancerpt
dc.typearticle-
degois.publication.firstPage14073pt
degois.publication.issue1pt
degois.publication.titleNature Communicationspt
dc.peerreviewedyespt
dc.identifier.doi10.1038/ncomms14073pt
degois.publication.volume8pt
dc.date.embargo2017-01-19*
uc.date.periodoEmbargo0pt
item.grantfulltextopen-
item.fulltextCom Texto completo-
item.openairetypearticle-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0003-1922-4824-
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais
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