Fkbp4 connects mtorc2 and pi3k to activate ...
Type de document :
Article dans une revue scientifique: Article original
DOI :
PMID :
URL permanente :
Titre :
Fkbp4 connects mtorc2 and pi3k to activate the pdk1/akt-dependent cell proliferation signaling in breast cancer
Auteur(s) :
Mange, Alain [Auteur]
Coyaud, Etienne-Marie [Auteur]
Desmetz, Caroline [Auteur]
Laurent, Estelle [Auteur]
Beganton, Benoit [Auteur]
Coopman, Peter [Auteur]
Raught, Brian [Auteur]
Solassol, Jerome [Auteur]
Coyaud, Etienne-Marie [Auteur]
Desmetz, Caroline [Auteur]
Laurent, Estelle [Auteur]
Beganton, Benoit [Auteur]
Coopman, Peter [Auteur]
Raught, Brian [Auteur]
Solassol, Jerome [Auteur]
Titre de la revue :
Theranostics
Nom court de la revue :
Theranostics
Numéro :
9
Pagination :
-
Date de publication :
2019-01-01
ISSN :
1838-7640
Mot(s)-clé(s) :
mTOR
FKBP52
FKBP4
BioID
AKT
breast cancer
FKBP52
FKBP4
BioID
AKT
breast cancer
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Purpose: Among the FKBP family members, FKBP4 has been described to have a potential role in tumorigenesis, and as a putative tissue marker. We previously showed that FKBP4, an HSP90-associated co-chaperone, can elicit ...
Lire la suite >Purpose: Among the FKBP family members, FKBP4 has been described to have a potential role in tumorigenesis, and as a putative tissue marker. We previously showed that FKBP4, an HSP90-associated co-chaperone, can elicit immune response as a tumor-specific antigen, and are overexpressed in breast cancer. Experimental design: In this study, we examined how loss of FKBP4 affect breast cancer progression and exploited protein interactomics to gain mechanistic insight into this process. Results: We found that FKBP4 expression is associated with breast cancer progression and prognosis, especially of ER-negative breast cancer. Furthermore, FKBP4 depletion specifically reduces cell growth and proliferation of triple negative breast cancer cell model and xenograft tumor model. Using specific protein interactome strategy by BirA proximity-dependent biotin identification, we demonstrated that FKBP4 is a novel PI3K-Akt-mTOR proximal interacting protein. Conclusion: Our results suggest that FKBP4 interacts with PI3K and can enhance Akt activation through PDK1 and mTORC2.Lire moins >
Lire la suite >Purpose: Among the FKBP family members, FKBP4 has been described to have a potential role in tumorigenesis, and as a putative tissue marker. We previously showed that FKBP4, an HSP90-associated co-chaperone, can elicit immune response as a tumor-specific antigen, and are overexpressed in breast cancer. Experimental design: In this study, we examined how loss of FKBP4 affect breast cancer progression and exploited protein interactomics to gain mechanistic insight into this process. Results: We found that FKBP4 expression is associated with breast cancer progression and prognosis, especially of ER-negative breast cancer. Furthermore, FKBP4 depletion specifically reduces cell growth and proliferation of triple negative breast cancer cell model and xenograft tumor model. Using specific protein interactome strategy by BirA proximity-dependent biotin identification, we demonstrated that FKBP4 is a novel PI3K-Akt-mTOR proximal interacting protein. Conclusion: Our results suggest that FKBP4 interacts with PI3K and can enhance Akt activation through PDK1 and mTORC2.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
INSERM
Université de Lille
Université de Lille
Date de dépôt :
2022-06-15T13:59:09Z