review Open AccessTop 1% cited
PI3K/Akt/mTOR signaling pathway and targeted therapy for glioblastoma
Oncotarget · 2016 · Vol. 7(22) · pp. 33440–33450
Xiaoman Li(China Medical University)Changjing Wu(China Medical University)Nianci Chen(China Medical University)Huadi Gu(China Medical University)Allen Yen(The University of Texas Southwestern Medical Center)Liu Cao(China Medical University)Enhua Wang(China Medical University)Liang Wang✉(China Medical University)
Abstract
Glioblastoma multiform (GBM) is the most common malignant glioma of all the brain tumors and currently effective treatment options are still lacking. GBM is frequently accompanied with overexpression and/or mutation of epidermal growth factor receptor (EGFR), which subsequently leads to activation of many downstream signal pathways such as phosphatidylinositol 3-kinase (PI3K)/Akt/rapamycin-sensitive mTOR-complex (mTOR) pathway. Here we explored the reason why inhibition of the pathway may serve as a compelling therapeutic target for the disease, and provided an update data of EFGR and PI3K/Akt/mTOR inhibitors in clinical trials.
PI3K/AKT/mTOR signaling in cancerCancer Mechanisms and TherapyHistone Deacetylase Inhibitors ResearchPI3K/AKT/mTOR pathwayProtein kinase BCancer researchMedicineGliomaSignal transductionRPTORTargeted therapyCancerBiology
MeSH terms
Phosphoinositide-3 Kinase InhibitorsAnimalsAntineoplastic AgentsBrain NeoplasmsGlioblastomaHumansSignal TransductionTreatment OutcomeProtein Kinase InhibitorsProto-Oncogene Proteins c-aktPhosphatidylinositol 3-KinaseTOR Serine-Threonine KinasesMolecular Targeted TherapyErbB Receptors
Funding
- National Natural Science Foundation of China
- Ministry of Education of the People's Republic of China
Citations
533
FWCI
27.15
field-weighted impact
References
94
Percentile
100%
vs. same field & year
Citations per year
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