Please use this identifier to cite or link to this item: https://hdl.handle.net/10316/108280
Title: Glucocorticoid receptor signalling activates YAP in breast cancer
Authors: Sorrentino, Giovanni
Ruggeri, Naomi
Zannini, Alessandro
Ingallina, Eleonora
Bertolio, Rebecca
Marotta, Carolina
Neri, Carmelo
Cappuzzello, Elisa
Forcato, Mattia
Rosato, Antonio
Mano, Miguel 
Bicciato, Silvio
Del Sal, Giannino
Issue Date: 19-Jan-2017
Project: grants 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. 
M.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), Portugal 
M.F. is supported by FIRB RBAP11T3WB and ERC grant no. 670126 Denovostem. 
metadata.degois.publication.title: Nature Communications
metadata.degois.publication.volume: 8
metadata.degois.publication.issue: 1
Abstract: The 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.
URI: https://hdl.handle.net/10316/108280
ISSN: 2041-1723
DOI: 10.1038/ncomms14073
Rights: openAccess
Appears in Collections:I&D CNC - Artigos em Revistas Internacionais

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