Retinoblastoma cells activate the AKT pathway and are vulnerable to the PI3K/mTOR inhibitor NVP-BEZ235

Retinoblastoma is a pediatric cancer of the retina most often caused by inactivation of the retinoblastoma (RB1) tumor suppressor gene. We previously showed that Rb1 loss cooperates with either co-activating the phosphatidylinositol 3-kinase (PI3K)/AKT pathway, or co-deleting Pten, to initiate retin...

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Detalles Bibliográficos
Autores principales: Xie, Chencheng, Freeman, Matthew J., Lu, Huarui, Wang, Xiaohong, Forster, Colleen L., Sarver, Aaron L., Hallstrom, Timothy C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Priority Research Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503517/
https://www.ncbi.nlm.nih.gov/pubmed/28445155
http://dx.doi.org/10.18632/oncotarget.16970

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5503517/
https://www.ncbi.nlm.nih.gov/pubmed/28445155
http://dx.doi.org/10.18632/oncotarget.16970

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