Negative regulation of PKB/Akt-dependent cell survival by the tumor suppressor PTEN

被引:2170
作者
Stambolic, V
Suzuki, A
de la Pompa, JL
Brothers, GM
Mirtsos, C
Sasaki, T
Ruland, J
Penninger, JM
Siderovski, DP
Mak, TW
机构
[1] Amgen Inst, Toronto, ON, Canada
[2] Univ Toronto, Ontario Canc Inst, Toronto, ON M5G 2C1, Canada
[3] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2C1, Canada
[4] Univ Toronto, Dept Immunol, Toronto, ON M5G 2C1, Canada
关键词
D O I
10.1016/S0092-8674(00)81780-8
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
PTEN is a tumor suppressor with sequence homology to protein tyrosine phosphatases and the cytoskeletal protein tensin. mPTEN-mutant mouse embryos display regions of increased proliferation. In contrast, mPTEN-deficient immortalized mouse embryonic fibroblasts exhibit decreased sensitivity to cell death in response to a number of apoptotic stimuli, accompanied by constitutively elevated activity and phosphorylation of protein kinase B/Akt, a crucial regulator of cell survival. Expression of exogenous PTEN in mutant cells restores both their sensitivity to agonist-induced apoptosis and normal pattern of PKB/Akt phosphorylation. Furthermore, PTEN negatively regulates intracellular levels of phosphatidylinositol (3,4,5) trisphosphate in cells and dephosphorylates it in vitro. Our results show that PTEN may exert its role as a tumor suppressor by negatively regulating the PI3'K/PKB/Akt signaling pathway.
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收藏
页码:29 / 39
页数:11
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