DJ-1, a novel regulator of the tumor suppressor PTEN

被引:480
作者
Kim, RH
Peters, M
Jang, YJ
Shi, W
Pintilie, M
Fletcher, GC
DeLuca, C
Liepa, J
Zhou, L
Snow, B
Binari, RC
Manoukian, AS
Bray, MR
Liu, FF
Tsao, MS
Mak, TW [1 ]
机构
[1] Adv Med Discovery Inst, Campbell Family Inst Breast Canc Res, Ontario Canc Inst, Toronto, ON M5G 2C1, Canada
[2] Univ Toronto, Dept Med Biophys, Toronto, ON M5G 2C1, Canada
[3] Princess Margaret Hosp, Dept Clin Informat, Toronto, ON M5G 2M9, Canada
[4] Princess Margaret Hosp, Dept Radiat Oncol, Toronto, ON M5G 2M9, Canada
[5] Princess Margaret Hosp, Dept Lab Med & Pathobiol, Toronto, ON M5G 2M9, Canada
[6] Miikana Therapeut Inc, Toronto, ON M5G 2C1, Canada
基金
加拿大健康研究院;
关键词
D O I
10.1016/j.ccr.2005.02.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The phosphatidylinositol 3' kinase (P13'K) pathway, which regulates cell survival, is antagonized by the PTEN tumor suppressor. The regulation of PTEN is unclear. A genetic screen of Drosophila gain-of-function mutants identified DJ-1 as a suppressor of PTEN function. In mammalian cells, DJ-1 underexpression results in decreased phosphorylation of PKB/ Akt, while DJ-1 overexpression leads to hyperphosphorylation of PKB/Akt and increased cell survival. In primary breast cancer samples, DJ-1 expression correlates negatively with PTEN immunoreactivity and positively with PKB/Akt hyperphosphorylation. In 19/23 primary non-small cell lung carcinoma samples, DJ-1 expression was increased compared to paired nonneoplastic lung tissue, and correlated positively with relapse incidence. DJ-1 is thus a key negative regulator of PTEN that may be a useful prognostic marker for cancer.
引用
收藏
页码:263 / 273
页数:11
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