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GGAP2/PIKE-A directly activates both the Akt and nuclear factor-κB pathways and promotes prostate cancer progression

  • Yi Cai
  • , Jianghua Wang
  • , Rile Li
  • , Gustavo Ayala
  • , Michael Ittmann
  • , Mingyao Liu*
  • *此作品的通讯作者
  • Texas A&M University System
  • Texas A&M University

科研成果: 期刊稿件文章同行评审

摘要

GGAP2/PIKE-A is a GTP-binding protein that can enhance Akt activity. Increased activation of the AKT and nuclear factor-κB (NF-κB) 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-κB and enhances NF-κB 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.

源语言英语
页(从-至)819-827
页数9
期刊Cancer Research
69
3
DOI
出版状态已出版 - 1 2月 2009
已对外发布

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