CORC  > 厦门大学  > 医学院-已发表论文
P21-activated protein kinase 1 induces colorectal cancer metastasis involving ERK activation and phosphorylation of FAK at Ser-910
Li, Liang-Hui ; Zheng, Min-Hua ; Luo, Qi ; Ye, Qing ; Feng, Bo ; Lu, Ai-Guo ; Wang, Ming-Liang ; Chen, Xue-Hua ; Su, Li-Ping ; Liu, Bing-Ya ; Luo Q(罗琪)
刊名http://dx.doi.org/10.3892/ijo_00000746
2010-10
关键词ACTIN CYTOSKELETON CELL-MIGRATION PAK1 GROWTH REORGANIZATION CARCINOMA ORGANIZATION EXPRESSION
英文摘要Pak1 has been reported to be overexpressed in colorectal cancer, but the role of Pak1 in colorectal cancer remains unclear. In this study, Pak1 expression and activity were associated with aggressive behavior of colorectal cancer. Overexpression of Pak1 increased colorectal cancer cell motility and invasion, whereas down-regulation of Pak1 expression or activity reduced colorectal cancer cell migration and invasion. In addition, activated Pak1 inhibited stress fiber and focal adhesion complex formation in colorectal cancer cells and led to formation of motile phenotypes. Importantly, activated Pak1 elicited phosphorylation of FAK at Ser-910 via an ERK-dependent pathway in colorectal cancer cell lines and clinical samples. In conclusion, our results suggest that activated Pak1 regulates colorectal cancer metastasis requiring an ERK-dependent phosphorylation of FAK at Ser-910.
语种英语
出版者INT J ONCOL
内容类型期刊论文
源URL[http://dspace.xmu.edu.cn/handle/2288/93178]  
专题医学院-已发表论文
推荐引用方式
GB/T 7714
Li, Liang-Hui,Zheng, Min-Hua,Luo, Qi,et al. P21-activated protein kinase 1 induces colorectal cancer metastasis involving ERK activation and phosphorylation of FAK at Ser-910[J]. http://dx.doi.org/10.3892/ijo_00000746,2010.
APA Li, Liang-Hui.,Zheng, Min-Hua.,Luo, Qi.,Ye, Qing.,Feng, Bo.,...&罗琪.(2010).P21-activated protein kinase 1 induces colorectal cancer metastasis involving ERK activation and phosphorylation of FAK at Ser-910.http://dx.doi.org/10.3892/ijo_00000746.
MLA Li, Liang-Hui,et al."P21-activated protein kinase 1 induces colorectal cancer metastasis involving ERK activation and phosphorylation of FAK at Ser-910".http://dx.doi.org/10.3892/ijo_00000746 (2010).
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