Molecular Pathways: Targeting Phosphoinositide 3-Kinase p110-Delta in Chronic Lymphocytic Leukemia

被引:42
|
作者
Herman, Sarah E. M. [2 ]
Johnson, Amy J. [1 ,3 ]
机构
[1] Ohio State Univ, Coll Pharm, Div Hematol, Dept Internal Med, Columbus, OH 43210 USA
[2] NHLBI, Hematol Branch, NIH, Bethesda, MD 20892 USA
[3] Ohio State Univ, Coll Pharm, Div Med Chem & Pharmacognosy, Columbus, OH 43210 USA
关键词
B-CELL ANTIGEN; PHOSPHATIDYLINOSITOL; 3-KINASE; PI3K ISOFORMS; ACTIVATION; INHIBITOR; CAL-101; DIFFERENTIATION; INSIGHTS; SUBUNIT; ROLES;
D O I
10.1158/1078-0432.CCR-11-1402
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The advent of targeted therapy, specifically to the B-cell receptor (BCR), has changed the convention for the treatment of chronic lymphocytic leukemia (CLL). The phosphoinositide 3-kinase (PI3K) pathway, activated upstream by the BCR, receptor tyrosine kinases, and cytokine receptors, has been a potential target for a multitude of cancers, but until the recent introduction of isoform-specific inhibitors has not been widely used. In this review, we focus on describing the intricate upstream and downstream signaling, leading to cell survival mediated by PI3K in B cells with a specific focus on the impact and importance of the p110 delta isoform (which is localized to hematopoietic cells and regulates distinct cellular functions in B cells). In addition, the clinical advances from targeting p110 delta are described, with a focus on clinical outcome, toxicities, and rational combination therapies. The experiences with p110 delta in CLL have led to a more fundamental understanding of CLL signaling defects and may be predictive of other BCR-directed therapeutics. Clin Cancer Res; 18(15); 4013-8. (C)2012 AACR.
引用
收藏
页码:4013 / 4018
页数:6
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