| Texto completo | |
| Autor(es): Mostrar menos - |
Alvarenga, Arthur William
;
Machado, Luis Eduardo
;
Rodrigues, Bruna Roz
;
Sulla Lupinacci, Fernanda Cristina
;
Sanemastu, Paulo
;
Matta, Eduardo
;
Roffe, Martin
;
Bleggi Torres, Luis Fernando
;
da Cunha, Isabela Werneck
;
Martins, Vilma Regina
;
Maroso Hajj, Glaucia Noeli
Número total de Autores: 11
|
| Tipo de documento: | Artigo Científico |
| Fonte: | JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY; v. 65, n. 2, p. 93-103, FEB 2017. |
| Citações Web of Science: | 9 |
| Resumo | |
The mammalian target of rapamycin (mTOR) binds to several protein partners and forms two complexes, termed mTOR complexes 1 and 2 (mTORC1/2), that differ in components, substrates, and regulation. mTORC2 contains the protein Rapamycin-insensitive companion of mTOR (RICTOR); phosphorylates kinases of the AGC family, such as Akt; and controls the cytoskeleton. Even though the regulation of mTORC2 activity remains poorly understood, the hyperactivation of this signaling pathway has been shown to contribute to the oncogenic properties of gliomas in experimental models. In this work, we evaluated expression and phosphorylation of Akt, and expression of RICTOR and Ki-67 in 195 human astrocytomas of different grades (38 cases of grade I, 49 grade II, 15 grade III, and 93 grade IV) and 30 normal brains. Expression and phosphorylation of Akt increased with histological grade and correlated with a worse overall survival in glioblastomas (GBMs). RICTOR was overexpressed in grade I and II astrocytomas and demonstrated a shift to nuclear localization in GBMs. Nuclear RICTOR was associated to increased proliferation in GBMs. Our results point to an increase in total and phosphorylated Akt in high-grade gliomas and to a possible role of RICTOR in proliferations of high-grade GBM cells. (AU) | |
| Processo FAPESP: | 14/15550-9 - Controle traducional no câncer |
| Beneficiário: | Glaucia Noeli Maroso Hajj |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |
| Processo FAPESP: | 09/14027-2 - Mecanismos associados à função da proteína prion e seu ligante STI1/Hop: abordagens terapêuticas |
| Beneficiário: | Vilma Regina Martins |
| Modalidade de apoio: | Auxílio à Pesquisa - Temático |