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High Mobility Group Box Protein 1 Serves as a Potential Prognostic Marker of Lung Cancer and Promotes Its Invasion and Metastasis by Matrix Metalloproteinase-2 in a Nuclear Factor-κB-Dependent Manner
Several studies have reported a significant role of high mobility group box protein 1 (HMGB1) in lung cancer. Nevertheless, there is a lack of knowledge regarding the expression of HMGB1 and its correlation with the clinicopathological features of lung cancer. In addition, the potential molecular me...
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Published in: | BioMed research international 2018-01, Vol.2018 (2018), p.1-7 |
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creator | Chen, Guangxia Mou, Jie Cui, Jinpeng Hu, Ankang E, Yunxiang Pei, Dongsheng Yu, Tao Yuan, Dawei Qin, Xiaobin Wang, Jindong Liu, Xiangqun Chen, Yuanyuan Wang, Weitao Wu, Xiaojin Mi, Yanyan |
description | Several studies have reported a significant role of high mobility group box protein 1 (HMGB1) in lung cancer. Nevertheless, there is a lack of knowledge regarding the expression of HMGB1 and its correlation with the clinicopathological features of lung cancer. In addition, the potential molecular mechanisms underlying the role of HMGB1 in lung cancer are still unknown. We therefore investigated the clinicopathological and prognostic significance as well as the potential role of HMGB1 in the development and progression of lung cancer. HMGB1 expression in the tumor tissues of the cohort correlated with clinicopathological features. Moreover, lung cell migration and invasion were significantly increased after treatment with HMGB1. The matrix metalloproteinase-2 (MMP-2) expression and activity were upregulated after treatment with HMGB1, while the upregulated expression of MMP-2 stimulated by HMGB1 in lung cancer cells was significantly reduced with the blockage of si-p65. These results indicated that HMGB1 expression was significantly associated with lung cancer progression. We also showed that HMGB1 promoted lung cancer invasion and metastasis by upregulating the expression and activity of MMP-2 in an NF-κB-dependent manner. Taken together, these data suggested that HMGB1 may be a potential prognosis and therapeutic marker for lung cancer. |
doi_str_mv | 10.1155/2018/3453706 |
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Nevertheless, there is a lack of knowledge regarding the expression of HMGB1 and its correlation with the clinicopathological features of lung cancer. In addition, the potential molecular mechanisms underlying the role of HMGB1 in lung cancer are still unknown. We therefore investigated the clinicopathological and prognostic significance as well as the potential role of HMGB1 in the development and progression of lung cancer. HMGB1 expression in the tumor tissues of the cohort correlated with clinicopathological features. Moreover, lung cell migration and invasion were significantly increased after treatment with HMGB1. The matrix metalloproteinase-2 (MMP-2) expression and activity were upregulated after treatment with HMGB1, while the upregulated expression of MMP-2 stimulated by HMGB1 in lung cancer cells was significantly reduced with the blockage of si-p65. These results indicated that HMGB1 expression was significantly associated with lung cancer progression. We also showed that HMGB1 promoted lung cancer invasion and metastasis by upregulating the expression and activity of MMP-2 in an NF-κB-dependent manner. Taken together, these data suggested that HMGB1 may be a potential prognosis and therapeutic marker for lung cancer.</description><identifier>ISSN: 2314-6133</identifier><identifier>EISSN: 2314-6141</identifier><identifier>DOI: 10.1155/2018/3453706</identifier><identifier>PMID: 29850505</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Biomarkers, Tumor - metabolism ; Cancer ; Cell growth ; Cell Line, Tumor ; Cell migration ; Enzyme Activation ; Female ; Gelatinase A ; High mobility group proteins ; HMGB1 protein ; HMGB1 Protein - metabolism ; Humans ; Inflammation ; Lung cancer ; Lung Neoplasms - enzymology ; Lung Neoplasms - pathology ; Male ; Matrix metalloproteinase ; Matrix Metalloproteinase 2 - metabolism ; Medical prognosis ; Medical research ; Metalloproteinase ; Metastases ; Metastasis ; Middle Aged ; Mobility ; Molecular modelling ; Mortality ; Neoplasm Invasiveness ; Neoplasm Metastasis ; NF-kappa B - metabolism ; NF-κB protein ; Pancreatic cancer ; Prognosis ; Proteins ; RNA, Small Interfering - metabolism ; Signal Transduction ; Survival Analysis ; Tumors</subject><ispartof>BioMed research international, 2018-01, Vol.2018 (2018), p.1-7</ispartof><rights>Copyright © 2018 Xiaojin Wu et al.</rights><rights>Copyright © 2018 Xiaojin Wu et al.; This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2018 Xiaojin Wu et al. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-4347ee2c2b0f9520ede1bd7468245187adc61f93fd6828ea51ebc987338f7ad73</citedby><cites>FETCH-LOGICAL-c401t-4347ee2c2b0f9520ede1bd7468245187adc61f93fd6828ea51ebc987338f7ad73</cites><orcidid>0000-0002-8053-3741 ; 0000-0002-5303-3039</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2032395120/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2032395120?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,25753,27924,27925,37012,37013,44590,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29850505$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Huang, Tao</contributor><contributor>Tao Huang</contributor><creatorcontrib>Chen, Guangxia</creatorcontrib><creatorcontrib>Mou, Jie</creatorcontrib><creatorcontrib>Cui, Jinpeng</creatorcontrib><creatorcontrib>Hu, Ankang</creatorcontrib><creatorcontrib>E, Yunxiang</creatorcontrib><creatorcontrib>Pei, Dongsheng</creatorcontrib><creatorcontrib>Yu, Tao</creatorcontrib><creatorcontrib>Yuan, Dawei</creatorcontrib><creatorcontrib>Qin, Xiaobin</creatorcontrib><creatorcontrib>Wang, Jindong</creatorcontrib><creatorcontrib>Liu, Xiangqun</creatorcontrib><creatorcontrib>Chen, Yuanyuan</creatorcontrib><creatorcontrib>Wang, Weitao</creatorcontrib><creatorcontrib>Wu, Xiaojin</creatorcontrib><creatorcontrib>Mi, Yanyan</creatorcontrib><title>High Mobility Group Box Protein 1 Serves as a Potential Prognostic Marker of Lung Cancer and Promotes Its Invasion and Metastasis by Matrix Metalloproteinase-2 in a Nuclear Factor-κB-Dependent Manner</title><title>BioMed research international</title><addtitle>Biomed Res Int</addtitle><description>Several studies have reported a significant role of high mobility group box protein 1 (HMGB1) in lung cancer. Nevertheless, there is a lack of knowledge regarding the expression of HMGB1 and its correlation with the clinicopathological features of lung cancer. In addition, the potential molecular mechanisms underlying the role of HMGB1 in lung cancer are still unknown. We therefore investigated the clinicopathological and prognostic significance as well as the potential role of HMGB1 in the development and progression of lung cancer. HMGB1 expression in the tumor tissues of the cohort correlated with clinicopathological features. Moreover, lung cell migration and invasion were significantly increased after treatment with HMGB1. The matrix metalloproteinase-2 (MMP-2) expression and activity were upregulated after treatment with HMGB1, while the upregulated expression of MMP-2 stimulated by HMGB1 in lung cancer cells was significantly reduced with the blockage of si-p65. These results indicated that HMGB1 expression was significantly associated with lung cancer progression. We also showed that HMGB1 promoted lung cancer invasion and metastasis by upregulating the expression and activity of MMP-2 in an NF-κB-dependent manner. Taken together, these data suggested that HMGB1 may be a potential prognosis and therapeutic marker for lung cancer.</description><subject>Biomarkers, Tumor - metabolism</subject><subject>Cancer</subject><subject>Cell growth</subject><subject>Cell Line, Tumor</subject><subject>Cell migration</subject><subject>Enzyme Activation</subject><subject>Female</subject><subject>Gelatinase A</subject><subject>High mobility group proteins</subject><subject>HMGB1 protein</subject><subject>HMGB1 Protein - metabolism</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Lung cancer</subject><subject>Lung Neoplasms - enzymology</subject><subject>Lung Neoplasms - pathology</subject><subject>Male</subject><subject>Matrix metalloproteinase</subject><subject>Matrix Metalloproteinase 2 - metabolism</subject><subject>Medical prognosis</subject><subject>Medical research</subject><subject>Metalloproteinase</subject><subject>Metastases</subject><subject>Metastasis</subject><subject>Middle Aged</subject><subject>Mobility</subject><subject>Molecular modelling</subject><subject>Mortality</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Metastasis</subject><subject>NF-kappa B - metabolism</subject><subject>NF-κB protein</subject><subject>Pancreatic cancer</subject><subject>Prognosis</subject><subject>Proteins</subject><subject>RNA, Small Interfering - metabolism</subject><subject>Signal Transduction</subject><subject>Survival Analysis</subject><subject>Tumors</subject><issn>2314-6133</issn><issn>2314-6141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNqNkkuP0zAQxyMEYldlb5yRJS5IENbPPC5IbGEfUgsrAefIcSatl9QudlK2X41PwInPxGRbyuOEHxp75jd_j6VJkseMvmRMqVNOWXEqpBI5ze4lx1wwmWZMsvuHsxBHyUmMNxRHwTJaZg-TI14WiuI8Tr5f2sWSzH1tO9tvyUXww5qc-VtyHXwP1hFGPkDYQCQaF7lGp-ut7sb4wvnYW0PmOnyGQHxLZoNbkKl2Bq_aNSO0woxIrnrcbqOj9e4uModeR1w2knqLCn2wt3fOrvPr3dM6QsoJlqDJu8F0oAM516b3If3x7Sx9A2twDRaDyc5BeJQ8aHUX4WRvJ8mn87cfp5fp7P3F1fT1LDWSsj6VQuYA3PCatqXiFBpgdZPLrOBSsSLXjclYW4q2QU8BWjGoTVnkQhQtBnMxSV7tdNdDvYLGYAVBd9U62JUO28prW_0dcXZZLfymUqUQVEkUeLYXCP7LALGvVjYa6DrtwA-x4lTmJS9yPqJP_0Fv_BAcfg8pwUWpGNpJ8mJHmeBjDNAeimG0GrukGruk2ncJ4k_-_MAB_tUTCDzfAUvrGv3V_qccIAOt_k0zrgrOxU-F_tFA</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Chen, Guangxia</creator><creator>Mou, Jie</creator><creator>Cui, Jinpeng</creator><creator>Hu, Ankang</creator><creator>E, Yunxiang</creator><creator>Pei, Dongsheng</creator><creator>Yu, Tao</creator><creator>Yuan, Dawei</creator><creator>Qin, Xiaobin</creator><creator>Wang, Jindong</creator><creator>Liu, Xiangqun</creator><creator>Chen, Yuanyuan</creator><creator>Wang, Weitao</creator><creator>Wu, Xiaojin</creator><creator>Mi, Yanyan</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><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>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>7TK</scope><scope>7U7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CWDGH</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-8053-3741</orcidid><orcidid>https://orcid.org/0000-0002-5303-3039</orcidid></search><sort><creationdate>20180101</creationdate><title>High Mobility Group Box Protein 1 Serves as a Potential Prognostic Marker of Lung Cancer and Promotes Its Invasion and Metastasis by Matrix Metalloproteinase-2 in a Nuclear Factor-κB-Dependent Manner</title><author>Chen, Guangxia ; Mou, Jie ; Cui, Jinpeng ; Hu, Ankang ; E, Yunxiang ; Pei, Dongsheng ; Yu, Tao ; Yuan, Dawei ; Qin, Xiaobin ; Wang, Jindong ; Liu, Xiangqun ; Chen, Yuanyuan ; Wang, Weitao ; Wu, Xiaojin ; Mi, Yanyan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-4347ee2c2b0f9520ede1bd7468245187adc61f93fd6828ea51ebc987338f7ad73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Biomarkers, Tumor - 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Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>BioMed research international</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Guangxia</au><au>Mou, Jie</au><au>Cui, Jinpeng</au><au>Hu, Ankang</au><au>E, Yunxiang</au><au>Pei, Dongsheng</au><au>Yu, Tao</au><au>Yuan, Dawei</au><au>Qin, Xiaobin</au><au>Wang, Jindong</au><au>Liu, Xiangqun</au><au>Chen, Yuanyuan</au><au>Wang, Weitao</au><au>Wu, Xiaojin</au><au>Mi, Yanyan</au><au>Huang, Tao</au><au>Tao Huang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>High Mobility Group Box Protein 1 Serves as a Potential Prognostic Marker of Lung Cancer and Promotes Its Invasion and Metastasis by Matrix Metalloproteinase-2 in a Nuclear Factor-κB-Dependent Manner</atitle><jtitle>BioMed research international</jtitle><addtitle>Biomed Res Int</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>2018</volume><issue>2018</issue><spage>1</spage><epage>7</epage><pages>1-7</pages><issn>2314-6133</issn><eissn>2314-6141</eissn><abstract>Several studies have reported a significant role of high mobility group box protein 1 (HMGB1) in lung cancer. Nevertheless, there is a lack of knowledge regarding the expression of HMGB1 and its correlation with the clinicopathological features of lung cancer. In addition, the potential molecular mechanisms underlying the role of HMGB1 in lung cancer are still unknown. We therefore investigated the clinicopathological and prognostic significance as well as the potential role of HMGB1 in the development and progression of lung cancer. HMGB1 expression in the tumor tissues of the cohort correlated with clinicopathological features. Moreover, lung cell migration and invasion were significantly increased after treatment with HMGB1. The matrix metalloproteinase-2 (MMP-2) expression and activity were upregulated after treatment with HMGB1, while the upregulated expression of MMP-2 stimulated by HMGB1 in lung cancer cells was significantly reduced with the blockage of si-p65. These results indicated that HMGB1 expression was significantly associated with lung cancer progression. We also showed that HMGB1 promoted lung cancer invasion and metastasis by upregulating the expression and activity of MMP-2 in an NF-κB-dependent manner. Taken together, these data suggested that HMGB1 may be a potential prognosis and therapeutic marker for lung cancer.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>29850505</pmid><doi>10.1155/2018/3453706</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-8053-3741</orcidid><orcidid>https://orcid.org/0000-0002-5303-3039</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Biomarkers, Tumor - metabolism Cancer Cell growth Cell Line, Tumor Cell migration Enzyme Activation Female Gelatinase A High mobility group proteins HMGB1 protein HMGB1 Protein - metabolism Humans Inflammation Lung cancer Lung Neoplasms - enzymology Lung Neoplasms - pathology Male Matrix metalloproteinase Matrix Metalloproteinase 2 - metabolism Medical prognosis Medical research Metalloproteinase Metastases Metastasis Middle Aged Mobility Molecular modelling Mortality Neoplasm Invasiveness Neoplasm Metastasis NF-kappa B - metabolism NF-κB protein Pancreatic cancer Prognosis Proteins RNA, Small Interfering - metabolism Signal Transduction Survival Analysis Tumors |
title | High Mobility Group Box Protein 1 Serves as a Potential Prognostic Marker of Lung Cancer and Promotes Its Invasion and Metastasis by Matrix Metalloproteinase-2 in a Nuclear Factor-κB-Dependent Manner |
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