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
Hauptverfasser: Lee, Eo-Jin, Lee, Se-Jung, Kim, Sangtae, Cho, Seok-Cheol, Choi, Yung Hyun, Kim, Wun-Jae, Moon, Sung-Kwon
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container_issue 10
container_start_page 2025
container_title Cellular signalling
container_volume 25
creator Lee, Eo-Jin
Lee, Se-Jung
Kim, Sangtae
Cho, Seok-Cheol
Choi, Yung Hyun
Kim, Wun-Jae
Moon, Sung-Kwon
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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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><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. 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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. 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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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