The role of PTEN signaling perturbations in cancer and in targeted therapy

被引:293
作者
Keniry, M. [1 ,2 ]
Parsons, R. [1 ,2 ,3 ]
机构
[1] Columbia Univ, Dept Pathol, Inst Canc Genet, New York, NY 10032 USA
[2] Columbia Univ, Herbert Irving Comprehens Canc Ctr, New York, NY 10032 USA
[3] Columbia Univ, Med Ctr, Dept Med, New York, NY 10032 USA
关键词
PTEN; PI3K; AKT; targeted chemotherapy;
D O I
10.1038/onc.2008.248
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The PTEN tumor suppressor was discovered by its homozygous deletion and other mutations in cancer. Since then, PTEN has been shown to be a non-redundant, evolutionarily conserved phosphatase whose function affects diverse cellular progresses such as cell cycle progression, cell proliferation, chemotaxis, apoptosis, aging, muscle contractility, DNA damage response, angiogenesis and cell polarity. In accordance with its ability to influence multiple crucial cellular processes, PTEN has a major role in the pathogenesis of numerous diseases such as diabetes, autism and almost every cancer examined. This review will discuss the diverse ways in which PTEN signaling is modified in cancer, and how these changes correlate with and might possibly affect the action of targeted chemotherapy.
引用
收藏
页码:5477 / 5485
页数:9
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