China Oncology ›› 2014, Vol. 24 ›› Issue (5): 329-332.doi: 10.3969/j.issn.1007-3969.2014.05.002

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Effect of PTTG1 in the invasion of glioma cells

CHEN Wei-yi1, LI Xiao-long1, QI Yue-liang1, LI Hong-li2, YIN Chong-gao3, LIU Xiao-li3, ZHANG Bao-gang1, GUO Wen-jun1   

  1. 1. Department of Pathology, Weifang Medical University, Weifang Shandong 261053, China;
    2. Medicine Research Center, Weifang Medical University, Weifang Shandong 261053, China;
    3. College of Nursing, Weifang Medical University, Weifang Shandong 261053, China
  • Online:2014-05-30 Published:2014-05-26
  • Contact: GUO Wen-jun E-mail: 13963669930@163.com

Abstract:

Background and purpose: Numerous researches indicated that the expression of pituitary tumor transforming gene1 (PTTG1) was correlated with the severity of glioma tumors. However the specific mechanism of PTTG1 is not clear in glioma. In this study, we explored the role and significance of PTTG1 in the invasion of glioma cells. Methods: Western blot was used to detect the expression of PTTG1 protein in various glioma cell lines. siRNA plasmid was used to transfect U87 cells. Western blot was used to analyze the expression of PTTG1 protein in transfected U87 cells. Matrigel invasion assay was used to detect the invasive ability in the cells being transfected in vitro. Western blot was used to analyze epithelial growth factor (EGF) induced protein phosphorylation of ARK5 and Akt in the cells being transfected PTTG1 plasmid (siPTTG1/U87) and scrambled siRNA (Scr/U87). Results: The expression of PTTG1 protein was higher in all glioma cell lines. After transfection, the invasion of siPTTG1/U87 was obviously decreased after 5 min with EGF stimulation than the Scr/U87, the phosphorylation of ARK5 and Akt was significantly enhanced. However, whether or not the existence of EGF, the phosphorylation of ARK5 and Akt had no differences in siPTTG1/U87. Conclusion: In glioma cells, PTTG1 protein is high expressed and maybe have an important function in glioma cells invasion through Akt-ARK5 signaling pathway.

Key words: Glioma, Invasiveness, PTTG1, ARK5, siRNA