PTEN and the PI3-Kinase Pathway in Cancer

被引:965
作者
Chalhoub, Nader [1 ]
Baker, Suzanne J. [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
PIK3CA; tumor suppressor; phosphatase; mTOR; mutations; TUMOR-SUPPRESSOR GENE; LIPID PHOSPHATASE-ACTIVITY; MAMMARY EPITHELIAL-CELLS; HEMATOPOIETIC STEM-CELLS; GROWTH-FACTOR-BETA; PHOSPHATIDYLINOSITOL; 3-KINASE; ENDOMETRIAL CARCINOMA; SIGNAL-TRANSDUCTION; MUTATIONAL SPECTRA; CATALYTIC SUBUNIT;
D O I
10.1146/annurev.pathol.4.110807.092311
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
PI3-kinase and PTEN are major positive and negative regulators, respectively, of the PI3-kinase pathway, which regulates growth, survival, and proliferation. These key signaling components are two of the most frequently mutated proteins in human cancers, resulting in unregulated activation of PI3K signaling and providing irrefutable genetic evidence of the central role of this pathway in tumorigenesis. PTEN regulates PI3K signaling by dephosphorylating the lipid signaling intermediate PIP3, but PTEN may have additional phosphatase-independent activities,as well as other functions in the nucleus. In this review, we highlight Current work showing cancer-relevant complexities in the regulation of PTEN and PI3K activity, potential novel functions for PTEN, and feedback regulation within the pathway. The significance and complexity of PI3K signaling make it an important but challenging therapeutic target for cancer.
引用
收藏
页码:127 / 150
页数:24
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