The PI3K Pathway As Drug Target in Human Cancer

被引:1037
作者
Courtney, Kevin D.
Corcoran, Ryan B.
Engelman, Jeffrey A. [1 ]
机构
[1] Massachusetts Gen Hosp, Ctr Canc, Charlestown, MA 02129 USA
基金
美国国家卫生研究院;
关键词
PLECKSTRIN HOMOLOGY DOMAIN; PHOSPHOINOSITIDE; 3-KINASE; PROTEIN-KINASE; PIK3CA GENE; PHOSPHATIDYLINOSITOL; 3-KINASES; ONCOGENIC TRANSFORMATION; FUNCTIONAL-ANALYSIS; HUMAN OVARIAN; MICE LACKING; TUMOR-CELLS;
D O I
10.1200/JCO.2009.25.3641
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The phosphatidylinositol 3-kinase (PI3K) signaling axis impacts on cancer cell growth, survival, motility, and metabolism. This pathway is activated by several different mechanisms in cancers, including somatic mutation and amplification of genes encoding key components. In addition, PI3K signaling may serve integral functions for noncancerous cells in the tumor microenvironment. Consequently, therapeutics targeting the PI3K pathway are being developed at a rapid pace, and preclinical and early clinical studies are beginning to suggest specific strategies to effectively use them. However, the central role of PI3K signaling in a large array of diverse biologic processes raises concerns about its use in therapeutics and increases the need to develop sophisticated strategies for its use. In this review, we will discuss how PI3K signaling affects the growth and survival of tumor cells. From this vantage, we will consider how inhibitors of the PI3K signaling cascade, either alone or in combination with other therapeutics, can most effectively be used for the treatment of cancer. J Clin Oncol 28: 1075-1083. (C) 2010 by American Society of Clinical Oncology
引用
收藏
页码:1075 / 1083
页数:9
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