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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...
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Published in: | Journal of experimental & clinical cancer research 2021-03, Vol.40 (1), p.113-113, Article 113 |
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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 |
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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 & 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 & 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 - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>Open Access: DOAJ - Directory of Open Access Journals</collection><jtitle>Journal of experimental & 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 & 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> |
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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 |