| Literature DB >> 24378923 |
Hai Zhang1, Shanyu Cheng1, Min Zhang1, Xiuping Ma1, Li Zhang1, Yipin Wang1, Rong Rong1, Juan Ma1, Shukai Xia1, Mingzhan Du1, Feng Shi1, Jie Wang1, Qinyi Yang1, Xiaoming Bai1, Jing Leng1.
Abstract
Prostaglandin E2 (PGE2) has been implicated in hepatocellular carcinoma cell invasion. Recently, it was reported that Y box-binding protein 1 (YB-1) is closely correlated with malignancy. This study was designed to examine the mechanisms by which PGE2 increases YB-1 expression and promotes HCC cell invasion. PGE2 greatly enhanced HCC cell invasion through upregulation of the YB-1 protein, and the EP1 receptor is mainly responsible for this regulation. Src and EGFR were both activated by PGE2, which in turn increased the phosphorylation levels of p44/42 MAPK. Src, EGFR and p44/42 MAPK were all involved in PGE2-induced YB-1 expression. Chemical inhibitors and RNAi analysis all confirmed the role of mTOR complex 1 in YB-1 expression induced by PGE2. Furthermore, YB-1 was able to regulate the expression of a series of EMT-associated genes, which indicated that YB-1 could have the potential to control the epithelial-mesenchymal transition process in HCC cells. These findings reveal that PGE2 upregulated YB-1 expression through the EP1/Src/EGFR/p44/42 MAPK/mTOR pathway, which greatly enhanced HCC cell invasion. This study for the first time describes the mechanisms through which PGE2 regulates YB-1 expression and promotes HCC cell invasion.Entities:
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Year: 2013 PMID: 24378923 DOI: 10.3892/ijo.2013.2234
Source DB: PubMed Journal: Int J Oncol ISSN: 1019-6439 Impact factor: 5.650