4.6 Review

PTEN function: the long and the short of it

期刊

TRENDS IN BIOCHEMICAL SCIENCES
卷 39, 期 4, 页码 183-190

出版社

ELSEVIER SCIENCE LONDON
DOI: 10.1016/j.tibs.2014.02.006

关键词

PTEN; PTEN-Long; PI3K signaling

资金

  1. NCI NIH HHS [P01 CA097403, R01 CA184016, R01 CA082783, R01 CA155117] Funding Source: Medline

向作者/读者索取更多资源

Phosphatase and tensin homolog deleted on chromosome ten (PTEN) is a phosphatase that is frequently altered in cancer. PTEN has phosphatase-dependent and -independent roles, and genetic alterations in PTEN lead to deregulation of protein synthesis, the cell cycle, migration, growth, DNA repair, and survival signaling. PTEN localization, stability, conformation, and phosphatase activity are controlled by an array of protein-protein interactions and post-translational modifications. Thus, PTEN-interacting and -modifying proteins have profound effects on the tumor suppressive functions of PTEN. Moreover, recent studies identified mechanisms by which PTEN can exit cells, via either exosomal export or secretion, and act on neighboring cells. This review focuses on modes of PTEN protein regulation and ways in which perturbations in this regulation may lead to disease.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据