Interleukin-5 enhances the migration and invasion of bladder cancer cells via ERK1/2-mediated MMP-9/NF-κB/AP-1 pathway: Involvement of the p21WAF1 expression
Inflammatory cytokines may be a critical component of epithelial cancer progression. We examined the role of interleukin (IL)-5 in the migration of bladder cancer cells. The expression of IL-5 and its receptor IL-5Rα was enhanced in patients with muscle invasive bladder cancers (MIBC), and then it w...
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Veröffentlicht in: | Cellular signalling 2013-10, Vol.25 (10), p.2025-2038 |
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description | Inflammatory cytokines may be a critical component of epithelial cancer progression. We examined the role of interleukin (IL)-5 in the migration of bladder cancer cells. The expression of IL-5 and its receptor IL-5Rα was enhanced in patients with muscle invasive bladder cancers (MIBC), and then it was detected in bladder cancer cell lines 5637 and T-24. IL-5 increased migration and MMP-9 expression via activation of transcription factors NF-κB and AP-1, and induced activation of ERK1/2 and Jak-Stat signaling in both cells. Treatment with ERK1/2 inhibitor U0126 significantly inhibited induction of migration, MMP-9 expression, and activation of NF-κB and AP-1 in IL-5-treated cells. However, none of the Jak inhibitors affected the IL-5-induced migration of bladder cancer cells. Moreover, gene knockdown for IL-5Rα, using siRNA transfection, suppressed migration, ERK1/2 activation, MMP-9 expression, as well as the binding activation of NF-κB and AP-1 in IL-5-treated bladder cancer cells. Similar results were observed in βc siRNA (si-βc) transfected cells. Unexpectedly, IL-5 treatment resulted in significant induction of p21WAF1 in both cell lines. The p21WAF1-specific small interfering RNA inhibited IL-5-induced cell migration, ERK activity, MMP-9 expression, and activation of NF-κB and AP-1 in bladder cancer cells. The effects of IL-5-induced cell responses were confirmed by transfection of IL-5 gene, which demonstrated that p21WAF1 participates in the induction of cell migration, leading to an increase in ERK1/2-mediated MMP-9 expression through activation of NF-κB and AP-1 in IL-5-treated bladder cancer cells. These unexpected results provide a theoretical basis for the therapeutic targeting of IL-5 in bladder cancer.
•Present study identified IL-5 and IL-5Rα with enhanced expression in MIBC patients.•The binding of IL-5 to IL-5Rα receptor induces the migration of cancer cells.•IL-5 induces the migration of bladder cancer cells via MMP-9/NF-κB/AP-1 regulation.•ERK1/2 is indispensible for the IL-5-induced cell migration.•p21WAF1 is involved in IL-5-induced migration of bladder cancer cells. |
doi_str_mv | 10.1016/j.cellsig.2013.06.004 |
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•Present study identified IL-5 and IL-5Rα with enhanced expression in MIBC patients.•The binding of IL-5 to IL-5Rα receptor induces the migration of cancer cells.•IL-5 induces the migration of bladder cancer cells via MMP-9/NF-κB/AP-1 regulation.•ERK1/2 is indispensible for the IL-5-induced cell migration.•p21WAF1 is involved in IL-5-induced migration of bladder cancer cells.</description><identifier>ISSN: 0898-6568</identifier><identifier>EISSN: 1873-3913</identifier><identifier>DOI: 10.1016/j.cellsig.2013.06.004</identifier><identifier>PMID: 23770289</identifier><language>eng</language><publisher>England: Elsevier Inc</publisher><subject>Cell Line, Tumor ; Cell Movement - genetics ; Cyclin-Dependent Kinase Inhibitor p21 - metabolism ; ERK1/2 ; Gene Expression Regulation, Neoplastic ; Humans ; IL-5 ; IL-5Rα ; Interleukin-5 - metabolism ; MAP Kinase Signaling System - genetics ; Matrix Metalloproteinase 9 - metabolism ; Migration ; MMP-9 ; Muscle Neoplasms - metabolism ; Muscle Neoplasms - pathology ; Muscle Neoplasms - secondary ; Neoplasm Invasiveness - genetics ; NF-kappa B - metabolism ; p21WAF1 ; Transcription Factor AP-1 - metabolism ; Urinary Bladder Neoplasms - genetics ; Urinary Bladder Neoplasms - metabolism ; Urinary Bladder Neoplasms - pathology</subject><ispartof>Cellular signalling, 2013-10, Vol.25 (10), p.2025-2038</ispartof><rights>2013 Elsevier Inc.</rights><rights>Copyright © 2013 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c365t-f7d9f09d7a72c70135f35de67dd549be509540212eb7a8f3a2bafb9aa2d957bc3</citedby><cites>FETCH-LOGICAL-c365t-f7d9f09d7a72c70135f35de67dd549be509540212eb7a8f3a2bafb9aa2d957bc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.cellsig.2013.06.004$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>315,782,786,3552,27931,27932,46002</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23770289$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Eo-Jin</creatorcontrib><creatorcontrib>Lee, Se-Jung</creatorcontrib><creatorcontrib>Kim, Sangtae</creatorcontrib><creatorcontrib>Cho, Seok-Cheol</creatorcontrib><creatorcontrib>Choi, Yung Hyun</creatorcontrib><creatorcontrib>Kim, Wun-Jae</creatorcontrib><creatorcontrib>Moon, Sung-Kwon</creatorcontrib><title>Interleukin-5 enhances the migration and invasion of bladder cancer cells via ERK1/2-mediated MMP-9/NF-κB/AP-1 pathway: Involvement of the p21WAF1 expression</title><title>Cellular signalling</title><addtitle>Cell Signal</addtitle><description>Inflammatory cytokines may be a critical component of epithelial cancer progression. We examined the role of interleukin (IL)-5 in the migration of bladder cancer cells. The expression of IL-5 and its receptor IL-5Rα was enhanced in patients with muscle invasive bladder cancers (MIBC), and then it was detected in bladder cancer cell lines 5637 and T-24. IL-5 increased migration and MMP-9 expression via activation of transcription factors NF-κB and AP-1, and induced activation of ERK1/2 and Jak-Stat signaling in both cells. Treatment with ERK1/2 inhibitor U0126 significantly inhibited induction of migration, MMP-9 expression, and activation of NF-κB and AP-1 in IL-5-treated cells. However, none of the Jak inhibitors affected the IL-5-induced migration of bladder cancer cells. Moreover, gene knockdown for IL-5Rα, using siRNA transfection, suppressed migration, ERK1/2 activation, MMP-9 expression, as well as the binding activation of NF-κB and AP-1 in IL-5-treated bladder cancer cells. Similar results were observed in βc siRNA (si-βc) transfected cells. Unexpectedly, IL-5 treatment resulted in significant induction of p21WAF1 in both cell lines. The p21WAF1-specific small interfering RNA inhibited IL-5-induced cell migration, ERK activity, MMP-9 expression, and activation of NF-κB and AP-1 in bladder cancer cells. The effects of IL-5-induced cell responses were confirmed by transfection of IL-5 gene, which demonstrated that p21WAF1 participates in the induction of cell migration, leading to an increase in ERK1/2-mediated MMP-9 expression through activation of NF-κB and AP-1 in IL-5-treated bladder cancer cells. These unexpected results provide a theoretical basis for the therapeutic targeting of IL-5 in bladder cancer.
•Present study identified IL-5 and IL-5Rα with enhanced expression in MIBC patients.•The binding of IL-5 to IL-5Rα receptor induces the migration of cancer cells.•IL-5 induces the migration of bladder cancer cells via MMP-9/NF-κB/AP-1 regulation.•ERK1/2 is indispensible for the IL-5-induced cell migration.•p21WAF1 is involved in IL-5-induced migration of bladder cancer cells.</description><subject>Cell Line, Tumor</subject><subject>Cell Movement - genetics</subject><subject>Cyclin-Dependent Kinase Inhibitor p21 - metabolism</subject><subject>ERK1/2</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Humans</subject><subject>IL-5</subject><subject>IL-5Rα</subject><subject>Interleukin-5 - metabolism</subject><subject>MAP Kinase Signaling System - genetics</subject><subject>Matrix Metalloproteinase 9 - metabolism</subject><subject>Migration</subject><subject>MMP-9</subject><subject>Muscle Neoplasms - metabolism</subject><subject>Muscle Neoplasms - pathology</subject><subject>Muscle Neoplasms - secondary</subject><subject>Neoplasm Invasiveness - genetics</subject><subject>NF-kappa B - metabolism</subject><subject>p21WAF1</subject><subject>Transcription Factor AP-1 - metabolism</subject><subject>Urinary Bladder Neoplasms - genetics</subject><subject>Urinary Bladder Neoplasms - metabolism</subject><subject>Urinary Bladder Neoplasms - pathology</subject><issn>0898-6568</issn><issn>1873-3913</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcGO0zAQhi0EYsvCI4B85OLUdmo75oK6qy1U7MIKgThaTjzZuiROsNPAvgwPwkPwTCRq4cppNNI388_8P0LPGc0YZXK5zypomuTvMk5ZnlGZUbp6gBasUDnJNcsfogUtdEGkkMUZepLSnlImqOSP0RnPlaK80Av0cxsGiA0cvvpABIaws6GChIcd4NbfRTv4LmAbHPZhtGluuhqXjXUOIq5meCrzJXj0Fl99fMeWnLTgvB3A4ZubW6KX7zfk96-L5fqWMNzbYffd3r_C2zB2zQgthGFeOQv2nH1ZbxiGH32ENIs9RY9q2yR4dqrn6PPm6tPlW3L94c32cn1NqlyKgdTK6Zpqp6zilZr8EHUuHEjlnFjpEgTVYkU541AqW9S55aWtS20td1qossrP0cvj3j523w6QBtP6NL9lA3SHZNiKMckLxuWEiiNaxS6lCLXpo29tvDeMmjkaszenaMwcjaHSTNFMcy9OEody8uff1N8sJuD1EYDp0dFDNKnyMBnsfIRqMK7z_5H4AwYgouc</recordid><startdate>201310</startdate><enddate>201310</enddate><creator>Lee, Eo-Jin</creator><creator>Lee, Se-Jung</creator><creator>Kim, Sangtae</creator><creator>Cho, Seok-Cheol</creator><creator>Choi, Yung Hyun</creator><creator>Kim, Wun-Jae</creator><creator>Moon, Sung-Kwon</creator><general>Elsevier 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>7X8</scope></search><sort><creationdate>201310</creationdate><title>Interleukin-5 enhances the migration and invasion of bladder cancer cells via ERK1/2-mediated MMP-9/NF-κB/AP-1 pathway: Involvement of the p21WAF1 expression</title><author>Lee, Eo-Jin ; Lee, Se-Jung ; Kim, Sangtae ; Cho, Seok-Cheol ; Choi, Yung Hyun ; Kim, Wun-Jae ; Moon, Sung-Kwon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c365t-f7d9f09d7a72c70135f35de67dd549be509540212eb7a8f3a2bafb9aa2d957bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Cell Line, Tumor</topic><topic>Cell Movement - genetics</topic><topic>Cyclin-Dependent Kinase Inhibitor p21 - metabolism</topic><topic>ERK1/2</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Humans</topic><topic>IL-5</topic><topic>IL-5Rα</topic><topic>Interleukin-5 - metabolism</topic><topic>MAP Kinase Signaling System - genetics</topic><topic>Matrix Metalloproteinase 9 - metabolism</topic><topic>Migration</topic><topic>MMP-9</topic><topic>Muscle Neoplasms - metabolism</topic><topic>Muscle Neoplasms - pathology</topic><topic>Muscle Neoplasms - secondary</topic><topic>Neoplasm Invasiveness - genetics</topic><topic>NF-kappa B - metabolism</topic><topic>p21WAF1</topic><topic>Transcription Factor AP-1 - metabolism</topic><topic>Urinary Bladder Neoplasms - genetics</topic><topic>Urinary Bladder Neoplasms - metabolism</topic><topic>Urinary Bladder Neoplasms - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Eo-Jin</creatorcontrib><creatorcontrib>Lee, Se-Jung</creatorcontrib><creatorcontrib>Kim, Sangtae</creatorcontrib><creatorcontrib>Cho, Seok-Cheol</creatorcontrib><creatorcontrib>Choi, Yung Hyun</creatorcontrib><creatorcontrib>Kim, Wun-Jae</creatorcontrib><creatorcontrib>Moon, Sung-Kwon</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Cellular signalling</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Eo-Jin</au><au>Lee, Se-Jung</au><au>Kim, Sangtae</au><au>Cho, Seok-Cheol</au><au>Choi, Yung Hyun</au><au>Kim, Wun-Jae</au><au>Moon, Sung-Kwon</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interleukin-5 enhances the migration and invasion of bladder cancer cells via ERK1/2-mediated MMP-9/NF-κB/AP-1 pathway: Involvement of the p21WAF1 expression</atitle><jtitle>Cellular signalling</jtitle><addtitle>Cell Signal</addtitle><date>2013-10</date><risdate>2013</risdate><volume>25</volume><issue>10</issue><spage>2025</spage><epage>2038</epage><pages>2025-2038</pages><issn>0898-6568</issn><eissn>1873-3913</eissn><abstract>Inflammatory cytokines may be a critical component of epithelial cancer progression. We examined the role of interleukin (IL)-5 in the migration of bladder cancer cells. The expression of IL-5 and its receptor IL-5Rα was enhanced in patients with muscle invasive bladder cancers (MIBC), and then it was detected in bladder cancer cell lines 5637 and T-24. IL-5 increased migration and MMP-9 expression via activation of transcription factors NF-κB and AP-1, and induced activation of ERK1/2 and Jak-Stat signaling in both cells. Treatment with ERK1/2 inhibitor U0126 significantly inhibited induction of migration, MMP-9 expression, and activation of NF-κB and AP-1 in IL-5-treated cells. However, none of the Jak inhibitors affected the IL-5-induced migration of bladder cancer cells. Moreover, gene knockdown for IL-5Rα, using siRNA transfection, suppressed migration, ERK1/2 activation, MMP-9 expression, as well as the binding activation of NF-κB and AP-1 in IL-5-treated bladder cancer cells. Similar results were observed in βc siRNA (si-βc) transfected cells. Unexpectedly, IL-5 treatment resulted in significant induction of p21WAF1 in both cell lines. The p21WAF1-specific small interfering RNA inhibited IL-5-induced cell migration, ERK activity, MMP-9 expression, and activation of NF-κB and AP-1 in bladder cancer cells. The effects of IL-5-induced cell responses were confirmed by transfection of IL-5 gene, which demonstrated that p21WAF1 participates in the induction of cell migration, leading to an increase in ERK1/2-mediated MMP-9 expression through activation of NF-κB and AP-1 in IL-5-treated bladder cancer cells. These unexpected results provide a theoretical basis for the therapeutic targeting of IL-5 in bladder cancer.
•Present study identified IL-5 and IL-5Rα with enhanced expression in MIBC patients.•The binding of IL-5 to IL-5Rα receptor induces the migration of cancer cells.•IL-5 induces the migration of bladder cancer cells via MMP-9/NF-κB/AP-1 regulation.•ERK1/2 is indispensible for the IL-5-induced cell migration.•p21WAF1 is involved in IL-5-induced migration of bladder cancer cells.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>23770289</pmid><doi>10.1016/j.cellsig.2013.06.004</doi><tpages>14</tpages></addata></record> |
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subjects | Cell Line, Tumor Cell Movement - genetics Cyclin-Dependent Kinase Inhibitor p21 - metabolism ERK1/2 Gene Expression Regulation, Neoplastic Humans IL-5 IL-5Rα Interleukin-5 - metabolism MAP Kinase Signaling System - genetics Matrix Metalloproteinase 9 - metabolism Migration MMP-9 Muscle Neoplasms - metabolism Muscle Neoplasms - pathology Muscle Neoplasms - secondary Neoplasm Invasiveness - genetics NF-kappa B - metabolism p21WAF1 Transcription Factor AP-1 - metabolism Urinary Bladder Neoplasms - genetics Urinary Bladder Neoplasms - metabolism Urinary Bladder Neoplasms - pathology |
title | Interleukin-5 enhances the migration and invasion of bladder cancer cells via ERK1/2-mediated MMP-9/NF-κB/AP-1 pathway: Involvement of the p21WAF1 expression |
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