YAP overexpression promotes the epithelial-mesenchymal transition and chemoresistance in pancreatic cancer cells

被引:75
|
作者
Yuan, Yanli [1 ]
Li, Deyu [2 ]
Li, Haibo [2 ]
Wang, Liancai [2 ]
Tian, Guangjin [2 ]
Dong, Yadong [2 ]
机构
[1] Childrens Hosp Zhengzhou, Zhengzhou 450008, Henan, Peoples R China
[2] Henan Prov Peoples Hosp, Zhengzhou 450003, Henan, Peoples R China
关键词
pancreatic cancer; EMT; YAP; chemoresistance; YES-ASSOCIATED PROTEIN; GROWTH-FACTOR RECEPTOR; MULTIDRUG-RESISTANCE; HIPPO PATHWAY; UP-REGULATION; ACTIVATION; IDENTIFICATION; PROLIFERATION; GEMCITABINE; CONTRIBUTES;
D O I
10.3892/mmr.2015.4550
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The expression of Yes-associated protein (YAP) has been reported to be dysregulated in pancreatic cancer. However, its contributions to tumor formation and progression remain to be elucidated. The present study demonstrated that YAP overexpression promoted the epithelial-mesenchymal transition (EMT) in a manner associated with pancreatic cancer invasion in vitro. RNA interference-mediated silencing of YAP attenuated cell invasion in vitro. Mechanistically, the present study demonstrated that YAP overexpression fosters pancreatic cancer progression by inducing the EMT in pancreatic cancer cells by activating the AKT cascade, which can counteract the effect of gemcitabine. These data suggested that the YAP acts synergistically to promote pancreatic cancer progression by hyperactivation of AKT signaling. The present study revealed YAP as a potential therapeutic target for pancreatic cancer and a biomarker for predicting gemcitabine treatment response.
引用
收藏
页码:237 / 242
页数:6
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