Abstract
Glioblastoma (GBM) is one of the most lethal human cancers. Genomic analyses define the molecular architecture of GBM and highlight a central function for mechanistic target of rapamycin (mTOR) signaling. mTOR kinase exists in two multi- protein complexes, namely, mTORC1 and mTORC2. These complexes differ in terms of function, regulation and rapamycin sensitivity. mTORC1 is well established as a cancer drug target, whereas the functions of mTORC2 in cancer, including GBM, remains poorly understood. This study reviews the recent findings that demonstrate a central function of mTORC2 in regulating tumor growth, metabolic reprogramming, and targeted therapy resistance in GBM, which makes mTORC2 as a critical GBM drug target.
Original language | English (US) |
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Pages (from-to) | 255-263 |
Number of pages | 9 |
Journal | Cancer Biology and Medicine |
Volume | 11 |
Issue number | 4 |
DOIs | |
State | Published - Dec 1 2014 |
Externally published | Yes |
Keywords
- Glioblastoma
- Metabolic reprogramming
- MTOR
- MTORC2
- PI3K
- Warburg effect
ASJC Scopus subject areas
- Oncology
- Cancer Research