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PTEN/MMAC1肿瘤抑制磷酸酶作为磷酸肌醇3激酶/Akt信号通路的负调节因子发挥作用。

The PTEN/MMAC1 tumor suppressor phosphatase functions as a negative regulator of the phosphoinositide 3-kinase/Akt pathway.

作者信息

Wu X, Senechal K, Neshat M S, Whang Y E, Sawyers C L

机构信息

Department of Medicine, University of California School of Medicine, Los Angeles, CA 90095, USA.

出版信息

Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15587-91. doi: 10.1073/pnas.95.26.15587.

Abstract

The PTEN/MMAC1 phosphatase is a tumor suppressor gene implicated in a wide range of human cancers. Here we provide biochemical and functional evidence that PTEN/MMAC1 acts a negative regulator of the phosphoinositide 3-kinase (PI3-kinase)/Akt pathway. PTEN/MMAC1 impairs activation of endogenous Akt in cells and inhibits phosphorylation of 4E-BP1, a downstream target of the PI3-kinase/Akt pathway involved in protein translation, whereas a catalytically inactive, dominant negative PTEN/MMAC1 mutant enhances 4E-BP1 phosphorylation. In addition, PTEN/MMAC1 represses gene expression in a manner that is rescued by Akt but not PI3-kinase. Finally, higher levels of Akt activation are observed in human prostate cancer cell lines and xenografts lacking PTEN/MMAC1 expression when compared with PTEN/MMAC1-positive prostate tumors or normal prostate tissue. Because constitutive activation of either PI3-kinase or Akt is known to induce cellular transformation, an increase in the activation of this pathway caused by mutations in PTEN/MMAC1 provides a potential mechanism for its tumor suppressor function.

摘要

PTEN/MMAC1磷酸酶是一种肿瘤抑制基因,与多种人类癌症相关。在此,我们提供了生化和功能证据,表明PTEN/MMAC1作为磷酸肌醇3激酶(PI3激酶)/Akt信号通路的负调节因子发挥作用。PTEN/MMAC1损害细胞内源性Akt的激活,并抑制4E-BP1的磷酸化,4E-BP1是PI3激酶/Akt信号通路中参与蛋白质翻译的下游靶点,而催化失活的显性负性PTEN/MMAC1突变体增强4E-BP1的磷酸化。此外,PTEN/MMAC1以一种可被Akt而非PI3激酶挽救的方式抑制基因表达。最后,与PTEN/MMAC1阳性的前列腺肿瘤或正常前列腺组织相比,在缺乏PTEN/MMAC1表达的人类前列腺癌细胞系和异种移植瘤中观察到更高水平的Akt激活。由于已知PI3激酶或Akt的组成性激活会诱导细胞转化,PTEN/MMAC1突变导致该信号通路激活增加为其肿瘤抑制功能提供了一种潜在机制。

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