GGAP2/PIKE-A Directly Activates Both the Akt and Nuclear Factor-κB Pathways and Promotes Prostate Cancer Progression

被引:34
作者
Cai, Yi [1 ,2 ,3 ,4 ]
Wang, Jianghua [1 ,2 ]
Li, Rile [1 ]
Ayala, Gustavo [1 ]
Ittmann, Michael [1 ,2 ]
Liu, Mingyao [3 ,4 ]
机构
[1] Baylor Coll Med, Dept Pathol, Houston, TX 77030 USA
[2] Michael DeBakey Dept Vet Affairs Med Ctr, Houston, TX USA
[3] Texas A&M Univ Syst, Hlth Sci Ctr, Alkek Inst Biosci & Technol, Houston, TX 77030 USA
[4] Texas A&M Univ Syst, Hlth Sci Ctr, Dept Med Biochem & Genet, Houston, TX 77030 USA
关键词
COMPARATIVE GENOMIC HYBRIDIZATION; TUMOR-SUPPRESSOR GENE; GROWTH-FACTOR; BIOCHEMICAL RECURRENCE; CELL-GROWTH; E-SELECTIN; PIKE-A; EXPRESSION; PTEN; SURVIVAL;
D O I
10.1158/0008-5472.CAN-08-2537
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
GGAP2/PIKE-A is a GTP-binding protein that can enhance Akt activity. Increased activation of the AKT and nuclear factor-kappa B (NF-kappa B) pathways have been identified as critical steps in cancer initiation and progression in a variety of human cancers. We have found significantly increased expression GGAP2 in the majority of human prostate cancers and GGAP2 expression increases Akt activation in prostate cancer cells. Thus, increased GGAP2 expression is a common mechanism for enhancing the activity of the Akt pathway in prostate cancers. In addition, we have found that activated Akt can bind and phosphorylate GGAP2 at serine 629, which enhances GTP binding by GGAP2. Phosphorylated GGAP2 can bind the p50 subunit of NF-kappa B and enhances NF-kappa B transcriptional activity. When expressed in prostate cancer cells, GGAP2 enhances proliferation, foci formation, and tumor progression in vivo. Thus, increased GGAP2 expression, which is present in three quarters of human prostate cancers, can activate two critical pathways that have been linked to prostate cancer initiation and progression. [Cancer Res 2009;69(3):819-27]
引用
收藏
页码:819 / 827
页数:9
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