Loading…

Elafin promotes tumour metastasis and attenuates the anti-metastatic effects of erlotinib via binding to EGFR in hepatocellular carcinoma

Elafin is a serine protease inhibitor critical for host defence. We previously reported that Elafin was associated with the recurrence of early-stage hepatocellular carcinoma (HCC) after surgery. However, the exact role of Elafin in HCC remains obscure. HCC tissue microarrays were used to investigat...

Full description

Saved in:
Bibliographic Details
Published in:Journal of experimental & clinical cancer research 2021-03, Vol.40 (1), p.113-113, Article 113
Main Authors: Wang, Chenwei, Liao, Yadi, He, Wei, Zhang, Hong, Zuo, Dinglan, Liu, Wenwu, Yang, Zhiwen, Qiu, Jiliang, Yuan, Yichuan, Li, Kai, Zhang, Yuanping, Wang, Yongjin, Shi, Yunxing, Qiu, Yuxiong, Gao, Song, Yuan, Yunfei, Li, Binkui
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-c594t-9d3dbd4e42f24bfdbd64c2bfb3c91df896b16875917117b98a189e372fe6b9093
cites cdi_FETCH-LOGICAL-c594t-9d3dbd4e42f24bfdbd64c2bfb3c91df896b16875917117b98a189e372fe6b9093
container_end_page 113
container_issue 1
container_start_page 113
container_title Journal of experimental & clinical cancer research
container_volume 40
creator Wang, Chenwei
Liao, Yadi
He, Wei
Zhang, Hong
Zuo, Dinglan
Liu, Wenwu
Yang, Zhiwen
Qiu, Jiliang
Yuan, Yichuan
Li, Kai
Zhang, Yuanping
Wang, Yongjin
Shi, Yunxing
Qiu, Yuxiong
Gao, Song
Yuan, Yunfei
Li, Binkui
description Elafin is a serine protease inhibitor critical for host defence. We previously reported that Elafin was associated with the recurrence of early-stage hepatocellular carcinoma (HCC) after surgery. However, the exact role of Elafin in HCC remains obscure. HCC tissue microarrays were used to investigate the correlation between Elafin expression and the prognosis of HCC patients. In vitro migration, invasion and wound healing assays and in vivo lung metastasis models were used to determine the role of Elafin in HCC metastasis. Mass spectrometry, co-immunoprecipitation, western blotting, and immunofluorescence staining assays were performed to uncover the mechanism of Elafin in HCC. Dual-luciferase reporter and chromatin immunoprecipitation assays were employed to observe the transcriptional regulation of Elafin. Elafin expression was frequently increased in HCC tissues compared to normal tissues, and high Elafin expression in HCC tissues was correlated with aggressive tumour phenotypes and a poor prognosis in HCC patients. Elafin dramatically enhanced the metastasis of HCC cells both in vitro and in vivo by interacting with EGFR and activating EGFR/AKT signalling. Moreover, Elafin attenuated the suppressive effects of erlotinib on HCC metastasis. Besides, Elafin was transcriptionally regulated by Sp1 in HCC cells. Clinically, Elafin expression was positively correlated with Sp1, Vimentin, and EGFR signalling in both our HCC tissue microarrays and TCGA database analysis. Upregulation of Elafin by Sp1 enhanced HCC metastasis via EGFR/AKT pathway, and overexpression of Elafin attenuated the anti-metastatic effects of erlotinib, suggesting a valuable prognostic biomarker and therapeutic target for HCC.
doi_str_mv 10.1186/s13046-021-01904-y
format article
fullrecord <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_d32f1834c9094fe19af4714979d33670</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A657262082</galeid><doaj_id>oai_doaj_org_article_d32f1834c9094fe19af4714979d33670</doaj_id><sourcerecordid>A657262082</sourcerecordid><originalsourceid>FETCH-LOGICAL-c594t-9d3dbd4e42f24bfdbd64c2bfb3c91df896b16875917117b98a189e372fe6b9093</originalsourceid><addsrcrecordid>eNptkl2L1DAUhoso7rr6B7yQgCDedG0-mjQ3wrLMrgsLguh1SNOTmSxtMibpwvwE_7WZD9cZkQYaTp_3Tc7pW1VvcXOJccc_JUwbxuuG4LrBsmH15ll1jkXLayk5f360P6tepfTQNBxLLF9WZ5QKgbGU59Wvxait82gdwxQyJJTnKcwRTZB1KsslpP2AdM7gZ70DVlBK2dUHJDuDwFowOaFgEcQxZOddjx6dRr3zg_NLlANa3N58Q-WkFax1DgbGcR51REZH43yY9OvqhdVjgjeH90X142bx_fpLff_19u766r42rWS5lgMd-oEBI5aw3pY9Z4b0tqdG4sF2kveYd6KVuHQoetlp3EmggljgvWwkvaju9r5D0A9qHd2k40YF7dSuEOJS6ViaGkENlFjcUWaKjlnAUlsmMJOiXIJy0RSvz3uv9dxPMBjwOerxxPT0i3crtQyPSkjZCkqLwceDQQw_Z0hZTS5tZ6M9hDkp0jaciG6Pvv8HfSg_ypdRFQozSjoh27_UUpcGnLehnGu2puqKt4Jw0nSkUJf_ocozwORM8GBdqZ8IPhwJVqDHvEphnLMLPp2CZA-aGFKKYJ-GgRu1Ta3ap1aV1KpdatWmiN4dj_FJ8iem9DfgDuiU</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2514328795</pqid></control><display><type>article</type><title>Elafin promotes tumour metastasis and attenuates the anti-metastatic effects of erlotinib via binding to EGFR in hepatocellular carcinoma</title><source>Open Access: PubMed Central</source><source>Publicly Available Content Database</source><creator>Wang, Chenwei ; Liao, Yadi ; He, Wei ; Zhang, Hong ; Zuo, Dinglan ; Liu, Wenwu ; Yang, Zhiwen ; Qiu, Jiliang ; Yuan, Yichuan ; Li, Kai ; Zhang, Yuanping ; Wang, Yongjin ; Shi, Yunxing ; Qiu, Yuxiong ; Gao, Song ; Yuan, Yunfei ; Li, Binkui</creator><creatorcontrib>Wang, Chenwei ; Liao, Yadi ; He, Wei ; Zhang, Hong ; Zuo, Dinglan ; Liu, Wenwu ; Yang, Zhiwen ; Qiu, Jiliang ; Yuan, Yichuan ; Li, Kai ; Zhang, Yuanping ; Wang, Yongjin ; Shi, Yunxing ; Qiu, Yuxiong ; Gao, Song ; Yuan, Yunfei ; Li, Binkui</creatorcontrib><description>Elafin is a serine protease inhibitor critical for host defence. We previously reported that Elafin was associated with the recurrence of early-stage hepatocellular carcinoma (HCC) after surgery. However, the exact role of Elafin in HCC remains obscure. HCC tissue microarrays were used to investigate the correlation between Elafin expression and the prognosis of HCC patients. In vitro migration, invasion and wound healing assays and in vivo lung metastasis models were used to determine the role of Elafin in HCC metastasis. Mass spectrometry, co-immunoprecipitation, western blotting, and immunofluorescence staining assays were performed to uncover the mechanism of Elafin in HCC. Dual-luciferase reporter and chromatin immunoprecipitation assays were employed to observe the transcriptional regulation of Elafin. Elafin expression was frequently increased in HCC tissues compared to normal tissues, and high Elafin expression in HCC tissues was correlated with aggressive tumour phenotypes and a poor prognosis in HCC patients. Elafin dramatically enhanced the metastasis of HCC cells both in vitro and in vivo by interacting with EGFR and activating EGFR/AKT signalling. Moreover, Elafin attenuated the suppressive effects of erlotinib on HCC metastasis. Besides, Elafin was transcriptionally regulated by Sp1 in HCC cells. Clinically, Elafin expression was positively correlated with Sp1, Vimentin, and EGFR signalling in both our HCC tissue microarrays and TCGA database analysis. Upregulation of Elafin by Sp1 enhanced HCC metastasis via EGFR/AKT pathway, and overexpression of Elafin attenuated the anti-metastatic effects of erlotinib, suggesting a valuable prognostic biomarker and therapeutic target for HCC.</description><identifier>ISSN: 1756-9966</identifier><identifier>ISSN: 0392-9078</identifier><identifier>EISSN: 1756-9966</identifier><identifier>DOI: 10.1186/s13046-021-01904-y</identifier><identifier>PMID: 33771199</identifier><language>eng</language><publisher>England: BioMed Central Ltd</publisher><subject>Analysis ; Antibodies ; Antineoplastic Combined Chemotherapy Protocols - pharmacology ; Antineoplastic Combined Chemotherapy Protocols - therapeutic use ; Cancer therapies ; Carcinoma, Hepatocellular - drug therapy ; Carcinoma, Hepatocellular - pathology ; Cell culture ; Chromatin ; Crystal structure ; Elafin ; Elafin - pharmacology ; Elafin - therapeutic use ; Epidermal growth factor ; Epidermal growth factor receptor ; ErbB Receptors ; Erlotinib ; Erlotinib Hydrochloride - pharmacology ; Erlotinib Hydrochloride - therapeutic use ; Female ; Gene amplification ; Health aspects ; Hepatocellular carcinoma ; Hepatoma ; Humans ; Liver cancer ; Liver Neoplasms - drug therapy ; Liver Neoplasms - pathology ; Male ; Mass spectrometry ; Metastasis ; Neoplasm Metastasis ; Plasmids ; Prognosis ; Protease inhibitors ; Protease Inhibitors - pharmacology ; Protease Inhibitors - therapeutic use ; Proteins ; Scientific imaging ; Survival analysis ; Targeted cancer therapy ; Thrombin ; Tumors</subject><ispartof>Journal of experimental &amp; clinical cancer research, 2021-03, Vol.40 (1), p.113-113, Article 113</ispartof><rights>COPYRIGHT 2021 BioMed Central Ltd.</rights><rights>2021. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>The Author(s) 2021, corrected publication 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c594t-9d3dbd4e42f24bfdbd64c2bfb3c91df896b16875917117b98a189e372fe6b9093</citedby><cites>FETCH-LOGICAL-c594t-9d3dbd4e42f24bfdbd64c2bfb3c91df896b16875917117b98a189e372fe6b9093</cites><orcidid>0000-0002-9694-9522</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7995733/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2514328795?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33771199$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wang, Chenwei</creatorcontrib><creatorcontrib>Liao, Yadi</creatorcontrib><creatorcontrib>He, Wei</creatorcontrib><creatorcontrib>Zhang, Hong</creatorcontrib><creatorcontrib>Zuo, Dinglan</creatorcontrib><creatorcontrib>Liu, Wenwu</creatorcontrib><creatorcontrib>Yang, Zhiwen</creatorcontrib><creatorcontrib>Qiu, Jiliang</creatorcontrib><creatorcontrib>Yuan, Yichuan</creatorcontrib><creatorcontrib>Li, Kai</creatorcontrib><creatorcontrib>Zhang, Yuanping</creatorcontrib><creatorcontrib>Wang, Yongjin</creatorcontrib><creatorcontrib>Shi, Yunxing</creatorcontrib><creatorcontrib>Qiu, Yuxiong</creatorcontrib><creatorcontrib>Gao, Song</creatorcontrib><creatorcontrib>Yuan, Yunfei</creatorcontrib><creatorcontrib>Li, Binkui</creatorcontrib><title>Elafin promotes tumour metastasis and attenuates the anti-metastatic effects of erlotinib via binding to EGFR in hepatocellular carcinoma</title><title>Journal of experimental &amp; clinical cancer research</title><addtitle>J Exp Clin Cancer Res</addtitle><description>Elafin is a serine protease inhibitor critical for host defence. We previously reported that Elafin was associated with the recurrence of early-stage hepatocellular carcinoma (HCC) after surgery. However, the exact role of Elafin in HCC remains obscure. HCC tissue microarrays were used to investigate the correlation between Elafin expression and the prognosis of HCC patients. In vitro migration, invasion and wound healing assays and in vivo lung metastasis models were used to determine the role of Elafin in HCC metastasis. Mass spectrometry, co-immunoprecipitation, western blotting, and immunofluorescence staining assays were performed to uncover the mechanism of Elafin in HCC. Dual-luciferase reporter and chromatin immunoprecipitation assays were employed to observe the transcriptional regulation of Elafin. Elafin expression was frequently increased in HCC tissues compared to normal tissues, and high Elafin expression in HCC tissues was correlated with aggressive tumour phenotypes and a poor prognosis in HCC patients. Elafin dramatically enhanced the metastasis of HCC cells both in vitro and in vivo by interacting with EGFR and activating EGFR/AKT signalling. Moreover, Elafin attenuated the suppressive effects of erlotinib on HCC metastasis. Besides, Elafin was transcriptionally regulated by Sp1 in HCC cells. Clinically, Elafin expression was positively correlated with Sp1, Vimentin, and EGFR signalling in both our HCC tissue microarrays and TCGA database analysis. Upregulation of Elafin by Sp1 enhanced HCC metastasis via EGFR/AKT pathway, and overexpression of Elafin attenuated the anti-metastatic effects of erlotinib, suggesting a valuable prognostic biomarker and therapeutic target for HCC.</description><subject>Analysis</subject><subject>Antibodies</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacology</subject><subject>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</subject><subject>Cancer therapies</subject><subject>Carcinoma, Hepatocellular - drug therapy</subject><subject>Carcinoma, Hepatocellular - pathology</subject><subject>Cell culture</subject><subject>Chromatin</subject><subject>Crystal structure</subject><subject>Elafin</subject><subject>Elafin - pharmacology</subject><subject>Elafin - therapeutic use</subject><subject>Epidermal growth factor</subject><subject>Epidermal growth factor receptor</subject><subject>ErbB Receptors</subject><subject>Erlotinib</subject><subject>Erlotinib Hydrochloride - pharmacology</subject><subject>Erlotinib Hydrochloride - therapeutic use</subject><subject>Female</subject><subject>Gene amplification</subject><subject>Health aspects</subject><subject>Hepatocellular carcinoma</subject><subject>Hepatoma</subject><subject>Humans</subject><subject>Liver cancer</subject><subject>Liver Neoplasms - drug therapy</subject><subject>Liver Neoplasms - pathology</subject><subject>Male</subject><subject>Mass spectrometry</subject><subject>Metastasis</subject><subject>Neoplasm Metastasis</subject><subject>Plasmids</subject><subject>Prognosis</subject><subject>Protease inhibitors</subject><subject>Protease Inhibitors - pharmacology</subject><subject>Protease Inhibitors - therapeutic use</subject><subject>Proteins</subject><subject>Scientific imaging</subject><subject>Survival analysis</subject><subject>Targeted cancer therapy</subject><subject>Thrombin</subject><subject>Tumors</subject><issn>1756-9966</issn><issn>0392-9078</issn><issn>1756-9966</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNptkl2L1DAUhoso7rr6B7yQgCDedG0-mjQ3wrLMrgsLguh1SNOTmSxtMibpwvwE_7WZD9cZkQYaTp_3Tc7pW1VvcXOJccc_JUwbxuuG4LrBsmH15ll1jkXLayk5f360P6tepfTQNBxLLF9WZ5QKgbGU59Wvxait82gdwxQyJJTnKcwRTZB1KsslpP2AdM7gZ70DVlBK2dUHJDuDwFowOaFgEcQxZOddjx6dRr3zg_NLlANa3N58Q-WkFax1DgbGcR51REZH43yY9OvqhdVjgjeH90X142bx_fpLff_19u766r42rWS5lgMd-oEBI5aw3pY9Z4b0tqdG4sF2kveYd6KVuHQoetlp3EmggljgvWwkvaju9r5D0A9qHd2k40YF7dSuEOJS6ViaGkENlFjcUWaKjlnAUlsmMJOiXIJy0RSvz3uv9dxPMBjwOerxxPT0i3crtQyPSkjZCkqLwceDQQw_Z0hZTS5tZ6M9hDkp0jaciG6Pvv8HfSg_ypdRFQozSjoh27_UUpcGnLehnGu2puqKt4Jw0nSkUJf_ocozwORM8GBdqZ8IPhwJVqDHvEphnLMLPp2CZA-aGFKKYJ-GgRu1Ta3ap1aV1KpdatWmiN4dj_FJ8iem9DfgDuiU</recordid><startdate>20210326</startdate><enddate>20210326</enddate><creator>Wang, Chenwei</creator><creator>Liao, Yadi</creator><creator>He, Wei</creator><creator>Zhang, Hong</creator><creator>Zuo, Dinglan</creator><creator>Liu, Wenwu</creator><creator>Yang, Zhiwen</creator><creator>Qiu, Jiliang</creator><creator>Yuan, Yichuan</creator><creator>Li, Kai</creator><creator>Zhang, Yuanping</creator><creator>Wang, Yongjin</creator><creator>Shi, Yunxing</creator><creator>Qiu, Yuxiong</creator><creator>Gao, Song</creator><creator>Yuan, Yunfei</creator><creator>Li, Binkui</creator><general>BioMed Central Ltd</general><general>BioMed Central</general><general>BMC</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>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-9694-9522</orcidid></search><sort><creationdate>20210326</creationdate><title>Elafin promotes tumour metastasis and attenuates the anti-metastatic effects of erlotinib via binding to EGFR in hepatocellular carcinoma</title><author>Wang, Chenwei ; Liao, Yadi ; He, Wei ; Zhang, Hong ; Zuo, Dinglan ; Liu, Wenwu ; Yang, Zhiwen ; Qiu, Jiliang ; Yuan, Yichuan ; Li, Kai ; Zhang, Yuanping ; Wang, Yongjin ; Shi, Yunxing ; Qiu, Yuxiong ; Gao, Song ; Yuan, Yunfei ; Li, Binkui</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c594t-9d3dbd4e42f24bfdbd64c2bfb3c91df896b16875917117b98a189e372fe6b9093</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Analysis</topic><topic>Antibodies</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacology</topic><topic>Antineoplastic Combined Chemotherapy Protocols - therapeutic use</topic><topic>Cancer therapies</topic><topic>Carcinoma, Hepatocellular - drug therapy</topic><topic>Carcinoma, Hepatocellular - pathology</topic><topic>Cell culture</topic><topic>Chromatin</topic><topic>Crystal structure</topic><topic>Elafin</topic><topic>Elafin - pharmacology</topic><topic>Elafin - therapeutic use</topic><topic>Epidermal growth factor</topic><topic>Epidermal growth factor receptor</topic><topic>ErbB Receptors</topic><topic>Erlotinib</topic><topic>Erlotinib Hydrochloride - pharmacology</topic><topic>Erlotinib Hydrochloride - therapeutic use</topic><topic>Female</topic><topic>Gene amplification</topic><topic>Health aspects</topic><topic>Hepatocellular carcinoma</topic><topic>Hepatoma</topic><topic>Humans</topic><topic>Liver cancer</topic><topic>Liver Neoplasms - drug therapy</topic><topic>Liver Neoplasms - pathology</topic><topic>Male</topic><topic>Mass spectrometry</topic><topic>Metastasis</topic><topic>Neoplasm Metastasis</topic><topic>Plasmids</topic><topic>Prognosis</topic><topic>Protease inhibitors</topic><topic>Protease Inhibitors - pharmacology</topic><topic>Protease Inhibitors - therapeutic use</topic><topic>Proteins</topic><topic>Scientific imaging</topic><topic>Survival analysis</topic><topic>Targeted cancer therapy</topic><topic>Thrombin</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wang, Chenwei</creatorcontrib><creatorcontrib>Liao, Yadi</creatorcontrib><creatorcontrib>He, Wei</creatorcontrib><creatorcontrib>Zhang, Hong</creatorcontrib><creatorcontrib>Zuo, Dinglan</creatorcontrib><creatorcontrib>Liu, Wenwu</creatorcontrib><creatorcontrib>Yang, Zhiwen</creatorcontrib><creatorcontrib>Qiu, Jiliang</creatorcontrib><creatorcontrib>Yuan, Yichuan</creatorcontrib><creatorcontrib>Li, Kai</creatorcontrib><creatorcontrib>Zhang, Yuanping</creatorcontrib><creatorcontrib>Wang, Yongjin</creatorcontrib><creatorcontrib>Shi, Yunxing</creatorcontrib><creatorcontrib>Qiu, Yuxiong</creatorcontrib><creatorcontrib>Gao, Song</creatorcontrib><creatorcontrib>Yuan, Yunfei</creatorcontrib><creatorcontrib>Li, Binkui</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Journal of experimental &amp; clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wang, Chenwei</au><au>Liao, Yadi</au><au>He, Wei</au><au>Zhang, Hong</au><au>Zuo, Dinglan</au><au>Liu, Wenwu</au><au>Yang, Zhiwen</au><au>Qiu, Jiliang</au><au>Yuan, Yichuan</au><au>Li, Kai</au><au>Zhang, Yuanping</au><au>Wang, Yongjin</au><au>Shi, Yunxing</au><au>Qiu, Yuxiong</au><au>Gao, Song</au><au>Yuan, Yunfei</au><au>Li, Binkui</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Elafin promotes tumour metastasis and attenuates the anti-metastatic effects of erlotinib via binding to EGFR in hepatocellular carcinoma</atitle><jtitle>Journal of experimental &amp; clinical cancer research</jtitle><addtitle>J Exp Clin Cancer Res</addtitle><date>2021-03-26</date><risdate>2021</risdate><volume>40</volume><issue>1</issue><spage>113</spage><epage>113</epage><pages>113-113</pages><artnum>113</artnum><issn>1756-9966</issn><issn>0392-9078</issn><eissn>1756-9966</eissn><abstract>Elafin is a serine protease inhibitor critical for host defence. We previously reported that Elafin was associated with the recurrence of early-stage hepatocellular carcinoma (HCC) after surgery. However, the exact role of Elafin in HCC remains obscure. HCC tissue microarrays were used to investigate the correlation between Elafin expression and the prognosis of HCC patients. In vitro migration, invasion and wound healing assays and in vivo lung metastasis models were used to determine the role of Elafin in HCC metastasis. Mass spectrometry, co-immunoprecipitation, western blotting, and immunofluorescence staining assays were performed to uncover the mechanism of Elafin in HCC. Dual-luciferase reporter and chromatin immunoprecipitation assays were employed to observe the transcriptional regulation of Elafin. Elafin expression was frequently increased in HCC tissues compared to normal tissues, and high Elafin expression in HCC tissues was correlated with aggressive tumour phenotypes and a poor prognosis in HCC patients. Elafin dramatically enhanced the metastasis of HCC cells both in vitro and in vivo by interacting with EGFR and activating EGFR/AKT signalling. Moreover, Elafin attenuated the suppressive effects of erlotinib on HCC metastasis. Besides, Elafin was transcriptionally regulated by Sp1 in HCC cells. Clinically, Elafin expression was positively correlated with Sp1, Vimentin, and EGFR signalling in both our HCC tissue microarrays and TCGA database analysis. Upregulation of Elafin by Sp1 enhanced HCC metastasis via EGFR/AKT pathway, and overexpression of Elafin attenuated the anti-metastatic effects of erlotinib, suggesting a valuable prognostic biomarker and therapeutic target for HCC.</abstract><cop>England</cop><pub>BioMed Central Ltd</pub><pmid>33771199</pmid><doi>10.1186/s13046-021-01904-y</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-9694-9522</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1756-9966
ispartof Journal of experimental & clinical cancer research, 2021-03, Vol.40 (1), p.113-113, Article 113
issn 1756-9966
0392-9078
1756-9966
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_d32f1834c9094fe19af4714979d33670
source Open Access: PubMed Central; Publicly Available Content Database
subjects Analysis
Antibodies
Antineoplastic Combined Chemotherapy Protocols - pharmacology
Antineoplastic Combined Chemotherapy Protocols - therapeutic use
Cancer therapies
Carcinoma, Hepatocellular - drug therapy
Carcinoma, Hepatocellular - pathology
Cell culture
Chromatin
Crystal structure
Elafin
Elafin - pharmacology
Elafin - therapeutic use
Epidermal growth factor
Epidermal growth factor receptor
ErbB Receptors
Erlotinib
Erlotinib Hydrochloride - pharmacology
Erlotinib Hydrochloride - therapeutic use
Female
Gene amplification
Health aspects
Hepatocellular carcinoma
Hepatoma
Humans
Liver cancer
Liver Neoplasms - drug therapy
Liver Neoplasms - pathology
Male
Mass spectrometry
Metastasis
Neoplasm Metastasis
Plasmids
Prognosis
Protease inhibitors
Protease Inhibitors - pharmacology
Protease Inhibitors - therapeutic use
Proteins
Scientific imaging
Survival analysis
Targeted cancer therapy
Thrombin
Tumors
title Elafin promotes tumour metastasis and attenuates the anti-metastatic effects of erlotinib via binding to EGFR in hepatocellular carcinoma
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T06%3A17%3A22IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Elafin%20promotes%20tumour%20metastasis%20and%20attenuates%20the%20anti-metastatic%20effects%20of%20erlotinib%20via%20binding%20to%20EGFR%20in%20hepatocellular%20carcinoma&rft.jtitle=Journal%20of%20experimental%20&%20clinical%20cancer%20research&rft.au=Wang,%20Chenwei&rft.date=2021-03-26&rft.volume=40&rft.issue=1&rft.spage=113&rft.epage=113&rft.pages=113-113&rft.artnum=113&rft.issn=1756-9966&rft.eissn=1756-9966&rft_id=info:doi/10.1186/s13046-021-01904-y&rft_dat=%3Cgale_doaj_%3EA657262082%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c594t-9d3dbd4e42f24bfdbd64c2bfb3c91df896b16875917117b98a189e372fe6b9093%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2514328795&rft_id=info:pmid/33771199&rft_galeid=A657262082&rfr_iscdi=true