Keniry M, Parsons R
Department of Pathology, Institute for Cancer Genetics and Herbert Irving Comprehensive Cancer Center, Columbia University, St Nicholas Avenue, New York, NY, USA.
Oncogene. 2008 Sep 18;27(41):5477-85. doi: 10.1038/onc.2008.248.
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.
PTEN肿瘤抑制基因是通过其在癌症中的纯合缺失和其他突变而被发现的。从那时起,PTEN已被证明是一种非冗余的、进化上保守的磷酸酶,其功能影响多种细胞进程,如细胞周期进程、细胞增殖、趋化性、凋亡、衰老、肌肉收缩性、DNA损伤反应、血管生成和细胞极性。鉴于其影响多个关键细胞过程的能力,PTEN在众多疾病(如糖尿病、自闭症以及几乎所有已检测的癌症)的发病机制中发挥着重要作用。本综述将讨论癌症中PTEN信号传导被改变的多种方式,以及这些变化如何与靶向化疗的作用相关联并可能对其产生影响。