Simultaneous inactivation of Par-4 and PTEN in vivo leads to synergistic NF-κB activation and invasive prostate carcinoma

被引:28
作者
Fernandez-Marcos, Pablo J. [2 ]
Abu-Baker, Shadi [1 ]
Joshi, Jayashree [1 ]
Galvez, Anita [1 ]
Castilla, Elias A. [1 ]
Canamero, Marta [2 ]
Collado, Manuel [2 ]
Saez, Carmen [3 ]
Moreno-Bueno, Gema [2 ]
Palacios, Jose [3 ]
Leitges, Michael [4 ]
Serrano, Manuel [2 ]
Moscat, Jorge [1 ]
Diaz-Meco, Maria T. [1 ]
机构
[1] Univ Cincinnati, Coll Med, Dept Canc & Cell Biol, Cincinnati, OH 45267 USA
[2] Spanish Natl Canc Res Ctr, Madrid 28029, Spain
[3] Univ Hosp Virgen del Rocio, Seville 41013, Spain
[4] Univ Oslo, Ctr Biotechnol, N-0317 Oslo, Norway
基金
美国国家卫生研究院;
关键词
AKT; aPKC; IL-6; inflammation; prostate cancer; TUMOR-SUPPRESSION; CANCER DEVELOPMENT; CELL-SURVIVAL; AKT; PATHWAY; TUMORIGENESIS; APOPTOSIS; KINASE; MOUSE; PROLIFERATION;
D O I
10.1073/pnas.0813055106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Prostate cancer is one of the most common neoplasias in men. The tumor suppressor Par-4 is an important negative regulator of the canonical NF-kappa B pathway and is highly expressed in prostate. Here we show that Par-4 expression is lost in a high percentage of human prostate carcinomas, and this occurs in association with phosphatase and tensin homolog deleted from chromosome 10 ( PTEN) loss. Par-4 null mice, similar to PTEN-heterozygous mice, only develop benign prostate lesions, but, importantly, concomitant Par-4 ablation and PTEN-heterozygosity lead to invasive prostate carcinoma in mice. This strong tumorigenic cooperation is anticipated in the preneoplastic prostate epithelium by an additive increase in Akt activation and a synergistic stimulation of NF-kappa B. These results establish the cooperation between Par-4 and PTEN as relevant for the development of prostate cancer and implicate the NF-kappa B pathway as a critical event in prostate tumorigenesis.
引用
收藏
页码:12962 / 12967
页数:6
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