Prostaglandin E2 promotes hepatocellular carcinoma cell invasion through upregulation of YB-1 protein expression

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...

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Veröffentlicht in:International journal of oncology 2014-03, Vol.44 (3), p.769-780
Hauptverfasser: ZHANG, HAI, CHENG, SHANYU, ZHANG, MIN, MA, XIUPING, ZHANG, LI, WANG, YIPIN, RONG, RONG, MA, JUAN, XIA, SHUKAI, DU, MINGZHAN, SHI, FENG, WANG, JIE, YANG, QINYI, BAI, XIAOMING, LENG, JING
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container_title International journal of oncology
container_volume 44
creator ZHANG, HAI
CHENG, SHANYU
ZHANG, MIN
MA, XIUPING
ZHANG, LI
WANG, YIPIN
RONG, RONG
MA, JUAN
XIA, SHUKAI
DU, MINGZHAN
SHI, FENG
WANG, JIE
YANG, QINYI
BAI, XIAOMING
LENG, JING
description 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.
doi_str_mv 10.3892/ijo.2013.2234
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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. 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subjects Angiogenesis
Breast cancer
Carcinoma, Hepatocellular - genetics
Carcinoma, Hepatocellular - pathology
Cell growth
Cell Line, Tumor
Dinoprostone - genetics
Dinoprostone - metabolism
Epithelial-Mesenchymal Transition - genetics
Gene expression
Gene Expression Regulation, Neoplastic
hepatocellular carcinoma
Humans
Hypotheses
Inflammation
invasion
Kinases
Liver cancer
Liver Neoplasms - genetics
Liver Neoplasms - pathology
Medical prognosis
Metastasis
Neoplasm Invasiveness - genetics
Neoplasm Invasiveness - pathology
Phosphorylation
prostaglandin E2
Proteins
RNA Interference
Signal transduction
Signal Transduction - genetics
Tumors
Y-box binding protein 1
Y-Box-Binding Protein 1 - biosynthesis
title Prostaglandin E2 promotes hepatocellular carcinoma cell invasion through upregulation of YB-1 protein expression
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