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 |
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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. 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.</description><identifier>ISSN: 1019-6439</identifier><identifier>EISSN: 1791-2423</identifier><identifier>DOI: 10.3892/ijo.2013.2234</identifier><identifier>PMID: 24378923</identifier><language>eng</language><publisher>Greece: D.A. Spandidos</publisher><subject>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</subject><ispartof>International journal of oncology, 2014-03, Vol.44 (3), p.769-780</ispartof><rights>Copyright © 2014, Spandidos Publications</rights><rights>Copyright Spandidos Publications UK Ltd. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3074-28b79ee56ee60d8363ae755b3b31a39e8f14670f80707a4fc0e28e3d9e66cf563</citedby><cites>FETCH-LOGICAL-c3074-28b79ee56ee60d8363ae755b3b31a39e8f14670f80707a4fc0e28e3d9e66cf563</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,5555,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24378923$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ZHANG, HAI</creatorcontrib><creatorcontrib>CHENG, SHANYU</creatorcontrib><creatorcontrib>ZHANG, MIN</creatorcontrib><creatorcontrib>MA, XIUPING</creatorcontrib><creatorcontrib>ZHANG, LI</creatorcontrib><creatorcontrib>WANG, YIPIN</creatorcontrib><creatorcontrib>RONG, RONG</creatorcontrib><creatorcontrib>MA, JUAN</creatorcontrib><creatorcontrib>XIA, SHUKAI</creatorcontrib><creatorcontrib>DU, MINGZHAN</creatorcontrib><creatorcontrib>SHI, FENG</creatorcontrib><creatorcontrib>WANG, JIE</creatorcontrib><creatorcontrib>YANG, QINYI</creatorcontrib><creatorcontrib>BAI, XIAOMING</creatorcontrib><creatorcontrib>LENG, JING</creatorcontrib><title>Prostaglandin E2 promotes hepatocellular carcinoma cell invasion through upregulation of YB-1 protein expression</title><title>International journal of oncology</title><addtitle>Int J Oncol</addtitle><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.</description><subject>Angiogenesis</subject><subject>Breast cancer</subject><subject>Carcinoma, Hepatocellular - genetics</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Dinoprostone - genetics</subject><subject>Dinoprostone - metabolism</subject><subject>Epithelial-Mesenchymal Transition - genetics</subject><subject>Gene expression</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>hepatocellular carcinoma</subject><subject>Humans</subject><subject>Hypotheses</subject><subject>Inflammation</subject><subject>invasion</subject><subject>Kinases</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - genetics</subject><subject>Liver Neoplasms - pathology</subject><subject>Medical prognosis</subject><subject>Metastasis</subject><subject>Neoplasm Invasiveness - genetics</subject><subject>Neoplasm Invasiveness - pathology</subject><subject>Phosphorylation</subject><subject>prostaglandin E2</subject><subject>Proteins</subject><subject>RNA Interference</subject><subject>Signal transduction</subject><subject>Signal Transduction - genetics</subject><subject>Tumors</subject><subject>Y-box binding protein 1</subject><subject>Y-Box-Binding Protein 1 - biosynthesis</subject><issn>1019-6439</issn><issn>1791-2423</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNo9kMtOxCAUQInR-F66NSQuXDECl0JZqvGVmOhCF64apr2d6aRTKrRG_16a0VlBLocDOYScCT6D3MqrZuVnkguYSQlqhxwKYwWTSsJu2nNhmVZgD8hRjCvOZZZxsU8OpAKTLsMh6V-Dj4NbtK6rmo7eSdoHv_YDRrrE3g2-xLYdWxdo6ULZdH7t6DSiTfflYuM7OiyDHxdLOvYBF4kcpqGv6ccNE5NswOTF73QaJ_6E7NWujXj6tx6T9_u7t9tH9vzy8HR7_cxK4EYxmc-NRcw0ouZVDhocmiybwxyEA4t5LZQ2vM654capuuQoc4TKotZlnWk4Jhcbb_rC54hxKFZ-DF16shAWJADXQiWKbagyZYgB66IPzdqFn0LwYupbpL7F1LeY-ib-_M86ztdYben_oAm43ACxn4pWPm6ZZGJKMQ6MG23hF5pxhHo</recordid><startdate>201403</startdate><enddate>201403</enddate><creator>ZHANG, HAI</creator><creator>CHENG, SHANYU</creator><creator>ZHANG, MIN</creator><creator>MA, XIUPING</creator><creator>ZHANG, LI</creator><creator>WANG, YIPIN</creator><creator>RONG, RONG</creator><creator>MA, JUAN</creator><creator>XIA, SHUKAI</creator><creator>DU, MINGZHAN</creator><creator>SHI, FENG</creator><creator>WANG, JIE</creator><creator>YANG, QINYI</creator><creator>BAI, XIAOMING</creator><creator>LENG, JING</creator><general>D.A. Spandidos</general><general>Spandidos Publications UK Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>201403</creationdate><title>Prostaglandin E2 promotes hepatocellular carcinoma cell invasion through upregulation of YB-1 protein expression</title><author>ZHANG, HAI ; CHENG, SHANYU ; ZHANG, MIN ; MA, XIUPING ; ZHANG, LI ; WANG, YIPIN ; RONG, RONG ; MA, JUAN ; XIA, SHUKAI ; DU, MINGZHAN ; SHI, FENG ; 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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. 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.</abstract><cop>Greece</cop><pub>D.A. Spandidos</pub><pmid>24378923</pmid><doi>10.3892/ijo.2013.2234</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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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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