Loading…

EGF is highly expressed in hepatocellular carcinoma (HCC) and promotes motility of HCC cells via fibronectin

Better understanding of metastasis process would allow for the development of effective approaches to treat hepatocellular carcinoma (HCC). Recent literature has highlighted the fundamental role of interaction between tumor cells and their microenvironment components in tumor metastasis. Aberrant ex...

Full description

Saved in:
Bibliographic Details
Published in:Journal of cellular biochemistry 2018-05, Vol.119 (5), p.4170-4183
Main Authors: Liu, Zongcai, Chen, Danyang, Ning, Fen, Du, Jun, Wang, Haifang
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c3535-b0c0f2f270763cd47df1d3ab8b1f1981d9a8bc07032ed7b8f0220ade1e4558c53
cites cdi_FETCH-LOGICAL-c3535-b0c0f2f270763cd47df1d3ab8b1f1981d9a8bc07032ed7b8f0220ade1e4558c53
container_end_page 4183
container_issue 5
container_start_page 4170
container_title Journal of cellular biochemistry
container_volume 119
creator Liu, Zongcai
Chen, Danyang
Ning, Fen
Du, Jun
Wang, Haifang
description Better understanding of metastasis process would allow for the development of effective approaches to treat hepatocellular carcinoma (HCC). Recent literature has highlighted the fundamental role of interaction between tumor cells and their microenvironment components in tumor metastasis. Aberrant expression of epidermal growth factor (EGF) induces highly malignant HCC, and activated EGF/EGFR signaling is correlated with an aggressive phenotype and intrahepatic metastasis. Thus, EGF in the tumor microenvironment may influence the behavior of HCC cells. In this study, for the first time, we studied the expression of EGF in HCCs, and the potential role of EGF in the motility of HCC cells and the underlying mechanisms. It was demonstrated that EGF was highly expressed in HCCs and positively associated with higher tumor grade. In addition, EGF promoted the migration and invasion of HCC cells mainly via induction of fibronectin (FN) in vitro. Mechanistically, EGF simultaneously increased the nuclear translocation and PKC mediated phosphorylation of p65 which could bind to the −356 bp to −259 bp fragment of FN promoter, leading to a markedly increased activity of FN promoter in HCC cells. These results highlight the potential role of EGF in promoting HCC metastasis, demonstrate a novel pathway for regulation of FN expression and provide potential targets for HCC prevention and treatment. Epidermal growth factor (EGF) was highly expressed in hepatocellular carcinoma (HCCs), and positively associated with higher tumor grade. In vitro, EGF promoted the migration and invasion of HCC cells mainly via induction of fibronectin (FN).
doi_str_mv 10.1002/jcb.26625
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1989555920</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2018051675</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3535-b0c0f2f270763cd47df1d3ab8b1f1981d9a8bc07032ed7b8f0220ade1e4558c53</originalsourceid><addsrcrecordid>eNp1kUtP3DAURi1EBcNjwR9AltjAInBtx3GypBGPVkjdlLXl-MF4lMRTO2k7_x4PA10gdXO9uMdHn-6H0BmBawJAb1a6u6ZVRfkeWhBoRFFWZbmPFiAYFJQReoiOUloBQNMweoAOacMIF5wvUH_3cI99wkv_suw32P5dR5uSNdiPeGnXagra9v3cq4i1itqPYVD48rFtr7AaDV7HMITJJpyn7_20wcHhvMXbXwn_9go738UwWj358QR9capP9vT9PUbP93c_28fi6cfDt_b2qdCMM150oMFRRwWIimlTCuOIYaqrO-JIUxPTqLrTIIBRa0RXO6AUlLHElpzXmrNjdLnz5ni_ZpsmOfi0TaRGG-Yks6ThnDcUMnrxCV2FOY45naRAauCkElvh1Y7SMaQUrZPr6AcVN5KA3FYgcwXyrYLMnr8b526w5h_5cfMM3OyAP763m_-b5Pf26075CseCjtM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2018051675</pqid></control><display><type>article</type><title>EGF is highly expressed in hepatocellular carcinoma (HCC) and promotes motility of HCC cells via fibronectin</title><source>Wiley</source><creator>Liu, Zongcai ; Chen, Danyang ; Ning, Fen ; Du, Jun ; Wang, Haifang</creator><creatorcontrib>Liu, Zongcai ; Chen, Danyang ; Ning, Fen ; Du, Jun ; Wang, Haifang</creatorcontrib><description>Better understanding of metastasis process would allow for the development of effective approaches to treat hepatocellular carcinoma (HCC). Recent literature has highlighted the fundamental role of interaction between tumor cells and their microenvironment components in tumor metastasis. Aberrant expression of epidermal growth factor (EGF) induces highly malignant HCC, and activated EGF/EGFR signaling is correlated with an aggressive phenotype and intrahepatic metastasis. Thus, EGF in the tumor microenvironment may influence the behavior of HCC cells. In this study, for the first time, we studied the expression of EGF in HCCs, and the potential role of EGF in the motility of HCC cells and the underlying mechanisms. It was demonstrated that EGF was highly expressed in HCCs and positively associated with higher tumor grade. In addition, EGF promoted the migration and invasion of HCC cells mainly via induction of fibronectin (FN) in vitro. Mechanistically, EGF simultaneously increased the nuclear translocation and PKC mediated phosphorylation of p65 which could bind to the −356 bp to −259 bp fragment of FN promoter, leading to a markedly increased activity of FN promoter in HCC cells. These results highlight the potential role of EGF in promoting HCC metastasis, demonstrate a novel pathway for regulation of FN expression and provide potential targets for HCC prevention and treatment. Epidermal growth factor (EGF) was highly expressed in hepatocellular carcinoma (HCCs), and positively associated with higher tumor grade. In vitro, EGF promoted the migration and invasion of HCC cells mainly via induction of fibronectin (FN).</description><identifier>ISSN: 0730-2312</identifier><identifier>EISSN: 1097-4644</identifier><identifier>DOI: 10.1002/jcb.26625</identifier><identifier>PMID: 29315755</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>Carcinoma, Hepatocellular - genetics ; Carcinoma, Hepatocellular - metabolism ; Carcinoma, Hepatocellular - pathology ; cell motility ; Cell Movement ; Epidermal growth factor ; epidermal growth factor (EGF) ; Epidermal Growth Factor - biosynthesis ; Epidermal Growth Factor - genetics ; Epidermal growth factor receptors ; Fibronectin ; Fibronectins - genetics ; Fibronectins - metabolism ; Gene Expression Regulation, Neoplastic ; Hep G2 Cells ; Hepatocellular carcinoma ; hepatocellular carcinoma (HCC) ; Humans ; Liver cancer ; Liver Neoplasms - genetics ; Liver Neoplasms - metabolism ; Liver Neoplasms - pathology ; Metastases ; Metastasis ; Motility ; Neoplasm Proteins - genetics ; Neoplasm Proteins - metabolism ; Nuclear transport ; Phenotypes ; Phosphorylation ; Protein kinase C ; Signaling ; Translocation ; Tumor cells ; tumor microenvironment</subject><ispartof>Journal of cellular biochemistry, 2018-05, Vol.119 (5), p.4170-4183</ispartof><rights>2018 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-b0c0f2f270763cd47df1d3ab8b1f1981d9a8bc07032ed7b8f0220ade1e4558c53</citedby><cites>FETCH-LOGICAL-c3535-b0c0f2f270763cd47df1d3ab8b1f1981d9a8bc07032ed7b8f0220ade1e4558c53</cites><orcidid>0000-0003-4872-0843</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29315755$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Zongcai</creatorcontrib><creatorcontrib>Chen, Danyang</creatorcontrib><creatorcontrib>Ning, Fen</creatorcontrib><creatorcontrib>Du, Jun</creatorcontrib><creatorcontrib>Wang, Haifang</creatorcontrib><title>EGF is highly expressed in hepatocellular carcinoma (HCC) and promotes motility of HCC cells via fibronectin</title><title>Journal of cellular biochemistry</title><addtitle>J Cell Biochem</addtitle><description>Better understanding of metastasis process would allow for the development of effective approaches to treat hepatocellular carcinoma (HCC). Recent literature has highlighted the fundamental role of interaction between tumor cells and their microenvironment components in tumor metastasis. Aberrant expression of epidermal growth factor (EGF) induces highly malignant HCC, and activated EGF/EGFR signaling is correlated with an aggressive phenotype and intrahepatic metastasis. Thus, EGF in the tumor microenvironment may influence the behavior of HCC cells. In this study, for the first time, we studied the expression of EGF in HCCs, and the potential role of EGF in the motility of HCC cells and the underlying mechanisms. It was demonstrated that EGF was highly expressed in HCCs and positively associated with higher tumor grade. In addition, EGF promoted the migration and invasion of HCC cells mainly via induction of fibronectin (FN) in vitro. Mechanistically, EGF simultaneously increased the nuclear translocation and PKC mediated phosphorylation of p65 which could bind to the −356 bp to −259 bp fragment of FN promoter, leading to a markedly increased activity of FN promoter in HCC cells. These results highlight the potential role of EGF in promoting HCC metastasis, demonstrate a novel pathway for regulation of FN expression and provide potential targets for HCC prevention and treatment. Epidermal growth factor (EGF) was highly expressed in hepatocellular carcinoma (HCCs), and positively associated with higher tumor grade. In vitro, EGF promoted the migration and invasion of HCC cells mainly via induction of fibronectin (FN).</description><subject>Carcinoma, Hepatocellular - genetics</subject><subject>Carcinoma, Hepatocellular - metabolism</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>cell motility</subject><subject>Cell Movement</subject><subject>Epidermal growth factor</subject><subject>epidermal growth factor (EGF)</subject><subject>Epidermal Growth Factor - biosynthesis</subject><subject>Epidermal Growth Factor - genetics</subject><subject>Epidermal growth factor receptors</subject><subject>Fibronectin</subject><subject>Fibronectins - genetics</subject><subject>Fibronectins - metabolism</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Hep G2 Cells</subject><subject>Hepatocellular carcinoma</subject><subject>hepatocellular carcinoma (HCC)</subject><subject>Humans</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - genetics</subject><subject>Liver Neoplasms - metabolism</subject><subject>Liver Neoplasms - pathology</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Motility</subject><subject>Neoplasm Proteins - genetics</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Nuclear transport</subject><subject>Phenotypes</subject><subject>Phosphorylation</subject><subject>Protein kinase C</subject><subject>Signaling</subject><subject>Translocation</subject><subject>Tumor cells</subject><subject>tumor microenvironment</subject><issn>0730-2312</issn><issn>1097-4644</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kUtP3DAURi1EBcNjwR9AltjAInBtx3GypBGPVkjdlLXl-MF4lMRTO2k7_x4PA10gdXO9uMdHn-6H0BmBawJAb1a6u6ZVRfkeWhBoRFFWZbmPFiAYFJQReoiOUloBQNMweoAOacMIF5wvUH_3cI99wkv_suw32P5dR5uSNdiPeGnXagra9v3cq4i1itqPYVD48rFtr7AaDV7HMITJJpyn7_20wcHhvMXbXwn_9go738UwWj358QR9capP9vT9PUbP93c_28fi6cfDt_b2qdCMM150oMFRRwWIimlTCuOIYaqrO-JIUxPTqLrTIIBRa0RXO6AUlLHElpzXmrNjdLnz5ni_ZpsmOfi0TaRGG-Yks6ThnDcUMnrxCV2FOY45naRAauCkElvh1Y7SMaQUrZPr6AcVN5KA3FYgcwXyrYLMnr8b526w5h_5cfMM3OyAP763m_-b5Pf26075CseCjtM</recordid><startdate>201805</startdate><enddate>201805</enddate><creator>Liu, Zongcai</creator><creator>Chen, Danyang</creator><creator>Ning, Fen</creator><creator>Du, Jun</creator><creator>Wang, Haifang</creator><general>Wiley Subscription Services, Inc</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>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7T7</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-4872-0843</orcidid></search><sort><creationdate>201805</creationdate><title>EGF is highly expressed in hepatocellular carcinoma (HCC) and promotes motility of HCC cells via fibronectin</title><author>Liu, Zongcai ; Chen, Danyang ; Ning, Fen ; Du, Jun ; Wang, Haifang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3535-b0c0f2f270763cd47df1d3ab8b1f1981d9a8bc07032ed7b8f0220ade1e4558c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Carcinoma, Hepatocellular - genetics</topic><topic>Carcinoma, Hepatocellular - metabolism</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>cell motility</topic><topic>Cell Movement</topic><topic>Epidermal growth factor</topic><topic>epidermal growth factor (EGF)</topic><topic>Epidermal Growth Factor - biosynthesis</topic><topic>Epidermal Growth Factor - genetics</topic><topic>Epidermal growth factor receptors</topic><topic>Fibronectin</topic><topic>Fibronectins - genetics</topic><topic>Fibronectins - metabolism</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Hep G2 Cells</topic><topic>Hepatocellular carcinoma</topic><topic>hepatocellular carcinoma (HCC)</topic><topic>Humans</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - genetics</topic><topic>Liver Neoplasms - metabolism</topic><topic>Liver Neoplasms - pathology</topic><topic>Metastases</topic><topic>Metastasis</topic><topic>Motility</topic><topic>Neoplasm Proteins - genetics</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Nuclear transport</topic><topic>Phenotypes</topic><topic>Phosphorylation</topic><topic>Protein kinase C</topic><topic>Signaling</topic><topic>Translocation</topic><topic>Tumor cells</topic><topic>tumor microenvironment</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Zongcai</creatorcontrib><creatorcontrib>Chen, Danyang</creatorcontrib><creatorcontrib>Ning, Fen</creatorcontrib><creatorcontrib>Du, Jun</creatorcontrib><creatorcontrib>Wang, Haifang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cellular biochemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Zongcai</au><au>Chen, Danyang</au><au>Ning, Fen</au><au>Du, Jun</au><au>Wang, Haifang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>EGF is highly expressed in hepatocellular carcinoma (HCC) and promotes motility of HCC cells via fibronectin</atitle><jtitle>Journal of cellular biochemistry</jtitle><addtitle>J Cell Biochem</addtitle><date>2018-05</date><risdate>2018</risdate><volume>119</volume><issue>5</issue><spage>4170</spage><epage>4183</epage><pages>4170-4183</pages><issn>0730-2312</issn><eissn>1097-4644</eissn><abstract>Better understanding of metastasis process would allow for the development of effective approaches to treat hepatocellular carcinoma (HCC). Recent literature has highlighted the fundamental role of interaction between tumor cells and their microenvironment components in tumor metastasis. Aberrant expression of epidermal growth factor (EGF) induces highly malignant HCC, and activated EGF/EGFR signaling is correlated with an aggressive phenotype and intrahepatic metastasis. Thus, EGF in the tumor microenvironment may influence the behavior of HCC cells. In this study, for the first time, we studied the expression of EGF in HCCs, and the potential role of EGF in the motility of HCC cells and the underlying mechanisms. It was demonstrated that EGF was highly expressed in HCCs and positively associated with higher tumor grade. In addition, EGF promoted the migration and invasion of HCC cells mainly via induction of fibronectin (FN) in vitro. Mechanistically, EGF simultaneously increased the nuclear translocation and PKC mediated phosphorylation of p65 which could bind to the −356 bp to −259 bp fragment of FN promoter, leading to a markedly increased activity of FN promoter in HCC cells. These results highlight the potential role of EGF in promoting HCC metastasis, demonstrate a novel pathway for regulation of FN expression and provide potential targets for HCC prevention and treatment. Epidermal growth factor (EGF) was highly expressed in hepatocellular carcinoma (HCCs), and positively associated with higher tumor grade. In vitro, EGF promoted the migration and invasion of HCC cells mainly via induction of fibronectin (FN).</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>29315755</pmid><doi>10.1002/jcb.26625</doi><tpages>14</tpages><orcidid>https://orcid.org/0000-0003-4872-0843</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0730-2312
ispartof Journal of cellular biochemistry, 2018-05, Vol.119 (5), p.4170-4183
issn 0730-2312
1097-4644
language eng
recordid cdi_proquest_miscellaneous_1989555920
source Wiley
subjects Carcinoma, Hepatocellular - genetics
Carcinoma, Hepatocellular - metabolism
Carcinoma, Hepatocellular - pathology
cell motility
Cell Movement
Epidermal growth factor
epidermal growth factor (EGF)
Epidermal Growth Factor - biosynthesis
Epidermal Growth Factor - genetics
Epidermal growth factor receptors
Fibronectin
Fibronectins - genetics
Fibronectins - metabolism
Gene Expression Regulation, Neoplastic
Hep G2 Cells
Hepatocellular carcinoma
hepatocellular carcinoma (HCC)
Humans
Liver cancer
Liver Neoplasms - genetics
Liver Neoplasms - metabolism
Liver Neoplasms - pathology
Metastases
Metastasis
Motility
Neoplasm Proteins - genetics
Neoplasm Proteins - metabolism
Nuclear transport
Phenotypes
Phosphorylation
Protein kinase C
Signaling
Translocation
Tumor cells
tumor microenvironment
title EGF is highly expressed in hepatocellular carcinoma (HCC) and promotes motility of HCC cells via fibronectin
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-23T14%3A24%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=EGF%20is%20highly%20expressed%20in%20hepatocellular%20carcinoma%20(HCC)%20and%20promotes%20motility%20of%20HCC%20cells%20via%20fibronectin&rft.jtitle=Journal%20of%20cellular%20biochemistry&rft.au=Liu,%20Zongcai&rft.date=2018-05&rft.volume=119&rft.issue=5&rft.spage=4170&rft.epage=4183&rft.pages=4170-4183&rft.issn=0730-2312&rft.eissn=1097-4644&rft_id=info:doi/10.1002/jcb.26625&rft_dat=%3Cproquest_cross%3E2018051675%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3535-b0c0f2f270763cd47df1d3ab8b1f1981d9a8bc07032ed7b8f0220ade1e4558c53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2018051675&rft_id=info:pmid/29315755&rfr_iscdi=true