The Role of Class IA Phosphatidylinositol-4,5-Bisphosphate 3-Kinase Catalytic Subunits in Glioblastoma

被引:22
作者
Pridham, Kevin J. [1 ,2 ]
Varghese, Robin T. [3 ]
Sheng, Zhi [1 ,4 ,5 ,6 ]
机构
[1] Virginia Tech, Virginia Tech Carilion Res Inst, Roanoke, VA 24016 USA
[2] Virginia Tech, Grad Program Translat Biol Med & Hlth, Blacksburg, VA USA
[3] Edward Via Coll Osteopath Med, Blacksburg, VA USA
[4] Virginia Tech, Virginia Tech Carilion Sch Med, Roanoke, VA 24016 USA
[5] Virginia Tech, Virginia Maryland Coll Vet Med, Dept Biomed Sci & Pathobiol, Blacksburg, VA 24016 USA
[6] Virginia Tech, Fac Hlth Sci, Blacksburg, VA 24016 USA
关键词
phosphatidylinositol-4,5-bisphosphate 3-kinase; glioblastoma; class IA phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunits; PIK3CA; PIK3CB; PIK3CD; REPORT PRIMARY BRAIN; RECURRENT GLIOBLASTOMA; PHASE-II; P110-ALPHA ISOFORM; ONCOGENIC MUTATION; SIGNALING PATHWAY; PIK3CA MUTATIONS; UNITED-STATES; PI3K ISOFORMS; CELL-GROWTH;
D O I
10.3389/fonc.2017.00312
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Phosphatidylinositol-4,5-bisphosphate 3-kinase (PI3K) plays a critical role in the pathogenesis of cancer including glioblastoma, the most common and aggressive form of brain cancer. Targeting the PI3K pathway to treat glioblastoma has been tested in the clinic with modest effect. In light of the recent finding that PI3K catalytic subunits (PIK3CA/p110 alpha, PIK3CB/p110 beta, PIK3CD/p110 delta, and PIK3CG/p110 gamma) are not functionally redundant, it is imperative to determine whether these subunits play divergent roles in glioblastoma and whether selectively targeting PI3K catalytic subunits represents a novel and effective strategy to tackle PI3K signaling. This article summarizes recent advances in understanding the role of PI3K catalytic subunits in glioblastoma and discusses the possibility of selective blockade of one PI3K catalytic subunit as a treatment option for glioblastoma.
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页数:8
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