eEF1A2 activates Akt and stimulates Akt-dependent actin remodeling, invasion and migration

被引:127
作者
Amiri, A. [1 ]
Noei, F. [1 ]
Jeganathan, S. [1 ]
Kulkarni, G. [1 ]
Pinke, D. E. [1 ]
Lee, J. M. [1 ]
机构
[1] Univ Ottawa, Dept Biochem Microbiol & Immunol, Ottawa, ON K1H 8M5, Canada
关键词
eEF1A2; Akt; filopodia; protein translation; actin; cell motility;
D O I
10.1038/sj.onc.1210101
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
eEF1A2 ( eukaryotic protein elongation factor 1 alpha 2) is a protein translation factor that is likely a human oncogene by virtue of its capacity to transform mammalian cells and its high expression in tumors of the ovary, breast and lung. Here, we show that expression of eEF1A2 is sufficient to stimulate the formation of filopodia in BT 549 human breast cancer cells and non-transformed Rat2 cells. Filopodia formation in eEF1A2-expressing cells is dependent on the activity of phosphatidylinositol-3 kinase ( PI3K), and the ROCK and Akt kinases. Furthermore, eEF1A2 expression is sufficient to activate Akt in a PI3K-dependent fashion and inactivation of eEF1A2 by short interfering RNA reduces Akt activity. Using breast cancer cell line BT 549, we show that eEF1A2 expression stimulates cell migration and invasion in a largely PI3K- and Akt-dependent manner. These results suggest that eEF1A2 regulates oncogenesis through Akt and PI3K-dependent cytoskeletal remodeling.
引用
收藏
页码:3027 / 3040
页数:14
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