Targeting Protein Kinases for the Treatment of Glioblastoma Multiforme: Linking Basic Studies to Clinical Applications

被引:3
|
作者
Zhou, Aidong [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Neurosurg, 6767 Bertner Ave, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
Glioblastoma; protein kinase; inhibitor; therapeutic strategy; clinical trials; combination treatment; GROWTH-FACTOR RECEPTOR; GLYCOGEN-SYNTHASE KINASE-3; PHASE-II TRIAL; BEVACIZUMAB PLUS IRINOTECAN; RECURRENT MALIGNANT GLIOMAS; INTEGRATED GENOMIC ANALYSIS; BRAIN-TUMOR CONSORTIUM; AKT INHIBITOR MK-2206; SRC FAMILY KINASE; CELL LUNG-CANCER;
D O I
10.2174/1381612823666170710144325
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Glioblastoma multiforme (GBM) is the most common malignant primary brain tumor in adults with intensive heterogeneity and one of the most lethal human cancers. Protein kinases control diverse cellular processes by coordinating different signaling pathways. Protein kinases are frequently dysregulated in human cancers, which contributes to tumor initiation and development. Thus, protein kinases are a growing drug target class for cancers including glioblastoma. This review focuses on the most important protein kinases and kinase-mediated signaling cascades in glioblastoma, and discusses the functional mechanism of these kinases in glioblastoma tumorigenesis. Moreover, this review has summarized the most recent preclinical and clinical advances of agents targeting protein kinases in the treatment of glioblastoma.
引用
收藏
页码:4290 / 4302
页数:13
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