Also, factors associated with integrin α5β1 were analyzed in our study. Integrin α5β1 could consequently activate many cytoskeleton proteins by binding to PRT062607 cell line FN, of which FAK and paxillin were crucial members [22–24]. It was shown that FAK phosphorylation

was required for integrin stimulated cell migration by creating a binding site for the Src kinase family. FAK could also phosphorylate paxillin by in vitro and in vivo studies [25, 26]. Paxillin was a cytoskeletal component involved in integrin signals integration and dissemination. this website phosphorylation of paxillin greatly enhanced its function during cell migration [27, 28]. Our study showed that exogenous AM treatment enhanced phosphorylation of FAK Tyr397 and paxillin Tyr118. The blocking antibody for integrin α5β1 mostly inhibited the AM induced upregulation of FAK and paxillin phosphorylation as well. Therefore, in our research, AM promoted HO8910 cells migration probably by upregulating expression of integrin α5β1 and increasing FAK and paxillin phosphorylation. However, the mechanisms of AM affection on integrin α5β1 needs further investigation, which might be owing to the

enhanced integrin-binding function of talin by AM [29]. Conclusions In the summary, we found that high expression of AM contributed to the progression of EOC and indicated poorer prognosis of EOC patients, which further demonstrated its contribution to EOC metastasis probably via integrin α5β1 mediated cell migration. All of which suggested that AM might play great roles during EOC cell migration, and might be considered VE-821 in vivo as an EOC therapeutic target. Acknowledgements This work was partly supported by the Liaoning Natural Science Foundation (no. 2009225035), the Liaoning Education Foundation (no. 2009A775), and the Shenyang Science and Technology Foundation (no. F11-262-9-14) to Yi Zhang. The authors declared no conflict of interests related to this study. References 1. Permuth-Wey J, Sellers TA: Epidemiology of ovarian cancer. Methods Mol Biology (Clifton, NJ) 2009, 472:413–437.CrossRef 2. Vang R,

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