Targeting therapeutic liabilities engendered by PIK3R1 mutations for cancer treatment

被引:51
作者
Cheung, Lydia W. T. [1 ]
Mills, Gordon B. [1 ,2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, Khalifa Bin Zayed Al Nahyan Inst Personalized Can, Houston, TX 77030 USA
关键词
MAPK; mutation; p85; PI3K; PIK3R1; targeted therapy; IA PHOSPHOINOSITIDE 3-KINASES; REGULATORY SUBUNIT P85-ALPHA; PI3K PATHWAY; ENDOMETRIAL CANCER; CLINICAL DEVELOPMENT; ANTITUMOR-ACTIVITY; CATALYTIC SUBUNIT; PTEN; ACTIVATION; INHIBITOR;
D O I
10.2217/pgs.15.174
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The regulatory subunit of PI3K, p85 alpha (encoded by PIK3R1), binds, stabilizes and inhibits the PI3K p110 catalytic subunit. Functional characterization of PIK3R1 mutations has identified not only hypomorphs with reduced inhibition of p110, but also hypomorphs and dominant negative mutants that disrupt a novel regulatory role of p85 alpha on PTEN or neomorphs that activate unexpected signaling pathways. The diverse phenotypic spectrum of these PIK3R1 driver mutations underscores the need for different treatment strategies targeting tumors harboring these mutations. This article describes the functional consequences of the spectrum of PIK3R1 driver mutations and therapeutic liabilities they may engender.
引用
收藏
页码:297 / 307
页数:11
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