Loading…

Human Leucine Zipper Protein sLZIP Induces Migration and Invasion of Cervical Cancer Cells via Expression of Matrix Metalloproteinase-9

Extracellular proteolysis mediates tissue homeostasis. In cancer, altered proteolysis leads to abnormal tumor growth, inflammation, tissue invasion, and metastasis. Matrix metalloproteinase-9 (MMP-9) represents one of the most prominent proteinases associated with inflammation and tumorigenesis. The...

Full description

Saved in:
Bibliographic Details
Published in:The Journal of biological chemistry 2011-12, Vol.286 (49), p.42072-42081
Main Authors: Kang, Hyereen, Jang, Sung-Wuk, Ko, Jesang
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-c442t-d697ee13c775462a40ac7fe016ec2944378ac285dbf0af8dbb39763c3d9372d3
cites cdi_FETCH-LOGICAL-c442t-d697ee13c775462a40ac7fe016ec2944378ac285dbf0af8dbb39763c3d9372d3
container_end_page 42081
container_issue 49
container_start_page 42072
container_title The Journal of biological chemistry
container_volume 286
creator Kang, Hyereen
Jang, Sung-Wuk
Ko, Jesang
description Extracellular proteolysis mediates tissue homeostasis. In cancer, altered proteolysis leads to abnormal tumor growth, inflammation, tissue invasion, and metastasis. Matrix metalloproteinase-9 (MMP-9) represents one of the most prominent proteinases associated with inflammation and tumorigenesis. The recently identified human transcription factor sLZIP is a member of the leucine zipper transcription factor family. Although sLZIP is known to function in ligand-induced transactivation of the glucocorticoid receptor, its exact functions and target genes are not known. In this study, we investigated the role of sLZIP in MMP-9 expression and its involvement in cervical cancer development. Our results show that sLZIP increased the expression of MMP-9 at both the mRNA and protein levels and the proteolytic activity of MMP-9 in HeLa and SiHa cells. sLZIP also increased the transcriptional activity of MMP-9 by binding directly to the cAMP-responsive element of the MMP-9 promoter region. Involvement of sLZIP in MMP-9 expression was further supported by the fact that ME-180 cells expressing sLZIP siRNA were refractory to MMP-9 expression. Results from wound healing and invasion assays showed that sLZIP enhanced both the migration and invasion of cervical cancer cells. The increased migration and invasion of HeLa and SiHa cells that were induced by sLZIP were abrogated by inhibition of the proteolytic activity of MMP-9. These results indicate that sLZIP plays a critical role in MMP-9 expression and is probably involved in invasion and metastasis of cervical cancer. Background: Proteolytic degradation of the extracellular matrix and basement membranes by matrix metalloproteinases (MMPs) is crucial in tumor invasion and metastasis. Results: sLZIP induces the expression of MMP-9, leading to enhancement of migration and invasion of cervical cancer cells. Conclusion: A novel regulatory mechanism of MMP-9 expression is characterized. Significance: sLZIP is a potential target for preventing the invasion and metastasis of cervical cancer.
doi_str_mv 10.1074/jbc.M111.272302
format article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3234971</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0021925820870975</els_id><sourcerecordid>908740070</sourcerecordid><originalsourceid>FETCH-LOGICAL-c442t-d697ee13c775462a40ac7fe016ec2944378ac285dbf0af8dbb39763c3d9372d3</originalsourceid><addsrcrecordid>eNp1kctu1DAUhi0EokNhzQ55xypT3zKON0hoVOhIM6KLLlA3lmOfFFcZO9hJVJ6A18ajtBUs8Mby8Xf-c_kRek_JmhIpLu5buz5QStdMMk7YC7SipOEVr-n3l2hFCKOVYnVzht7kfE_KEYq-RmeMEaJkTVbo99V0NAHvYbI-AL71wwAJX6c4gg84729313gX3GQh44O_S2b0MWATXInOJp8escNbSLO3psdbE2zJ30LfZzx7gy8fhgT5iTuYMfkHfIDR9H0cliomQ6Xeoled6TO8e7zP0c2Xy5vtVbX_9nW3_byvrBBsrNxGSQDKrZS12DAjiLGyA0I3YJkSgsvGWNbUru2I6RrXtlzJDbfcKS6Z4-fo0yI7TO0RnIUwJtPrIfmjSb90NF7_-xP8D30XZ80ZF0rSIvDxUSDFnxPkUR99tmVcEyBOWSvSSEGIJIW8WEibYs4JuucqlOiTebqYp0_m6cW8kvHh7-ae-Se3CqAWAMqGZg9JZ-uhbNz5BHbULvr_iv8B666reQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>908740070</pqid></control><display><type>article</type><title>Human Leucine Zipper Protein sLZIP Induces Migration and Invasion of Cervical Cancer Cells via Expression of Matrix Metalloproteinase-9</title><source>Open Access: PubMed Central</source><source>ScienceDirect®</source><creator>Kang, Hyereen ; Jang, Sung-Wuk ; Ko, Jesang</creator><creatorcontrib>Kang, Hyereen ; Jang, Sung-Wuk ; Ko, Jesang</creatorcontrib><description>Extracellular proteolysis mediates tissue homeostasis. In cancer, altered proteolysis leads to abnormal tumor growth, inflammation, tissue invasion, and metastasis. Matrix metalloproteinase-9 (MMP-9) represents one of the most prominent proteinases associated with inflammation and tumorigenesis. The recently identified human transcription factor sLZIP is a member of the leucine zipper transcription factor family. Although sLZIP is known to function in ligand-induced transactivation of the glucocorticoid receptor, its exact functions and target genes are not known. In this study, we investigated the role of sLZIP in MMP-9 expression and its involvement in cervical cancer development. Our results show that sLZIP increased the expression of MMP-9 at both the mRNA and protein levels and the proteolytic activity of MMP-9 in HeLa and SiHa cells. sLZIP also increased the transcriptional activity of MMP-9 by binding directly to the cAMP-responsive element of the MMP-9 promoter region. Involvement of sLZIP in MMP-9 expression was further supported by the fact that ME-180 cells expressing sLZIP siRNA were refractory to MMP-9 expression. Results from wound healing and invasion assays showed that sLZIP enhanced both the migration and invasion of cervical cancer cells. The increased migration and invasion of HeLa and SiHa cells that were induced by sLZIP were abrogated by inhibition of the proteolytic activity of MMP-9. These results indicate that sLZIP plays a critical role in MMP-9 expression and is probably involved in invasion and metastasis of cervical cancer. Background: Proteolytic degradation of the extracellular matrix and basement membranes by matrix metalloproteinases (MMPs) is crucial in tumor invasion and metastasis. Results: sLZIP induces the expression of MMP-9, leading to enhancement of migration and invasion of cervical cancer cells. Conclusion: A novel regulatory mechanism of MMP-9 expression is characterized. Significance: sLZIP is a potential target for preventing the invasion and metastasis of cervical cancer.</description><identifier>ISSN: 0021-9258</identifier><identifier>EISSN: 1083-351X</identifier><identifier>DOI: 10.1074/jbc.M111.272302</identifier><identifier>PMID: 22009750</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Cancer Biology ; Cell Invasion ; Cell Line, Tumor ; Cell Migration ; Cell Movement ; Cervical Cancer ; Cyclic AMP Response Element-Binding Protein - chemistry ; Female ; Gene Expression Regulation, Enzymologic ; Gene Expression Regulation, Neoplastic ; HeLa Cells ; Humans ; Matrix Metalloproteinase (MMP) ; Matrix Metalloproteinase 9 - biosynthesis ; Molecular Bases of Disease ; Neoplasm Invasiveness ; Neoplasm Metastasis ; Promoter Regions, Genetic ; Proteolysis ; RNA Interference ; sLZIP ; Transcription Factors ; Uterine Cervical Neoplasms - metabolism</subject><ispartof>The Journal of biological chemistry, 2011-12, Vol.286 (49), p.42072-42081</ispartof><rights>2011 © 2011 ASBMB. Currently published by Elsevier Inc; originally published by American Society for Biochemistry and Molecular Biology.</rights><rights>2011 by The American Society for Biochemistry and Molecular Biology, Inc. 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c442t-d697ee13c775462a40ac7fe016ec2944378ac285dbf0af8dbb39763c3d9372d3</citedby><cites>FETCH-LOGICAL-c442t-d697ee13c775462a40ac7fe016ec2944378ac285dbf0af8dbb39763c3d9372d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3234971/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0021925820870975$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,3549,27924,27925,45780,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22009750$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kang, Hyereen</creatorcontrib><creatorcontrib>Jang, Sung-Wuk</creatorcontrib><creatorcontrib>Ko, Jesang</creatorcontrib><title>Human Leucine Zipper Protein sLZIP Induces Migration and Invasion of Cervical Cancer Cells via Expression of Matrix Metalloproteinase-9</title><title>The Journal of biological chemistry</title><addtitle>J Biol Chem</addtitle><description>Extracellular proteolysis mediates tissue homeostasis. In cancer, altered proteolysis leads to abnormal tumor growth, inflammation, tissue invasion, and metastasis. Matrix metalloproteinase-9 (MMP-9) represents one of the most prominent proteinases associated with inflammation and tumorigenesis. The recently identified human transcription factor sLZIP is a member of the leucine zipper transcription factor family. Although sLZIP is known to function in ligand-induced transactivation of the glucocorticoid receptor, its exact functions and target genes are not known. In this study, we investigated the role of sLZIP in MMP-9 expression and its involvement in cervical cancer development. Our results show that sLZIP increased the expression of MMP-9 at both the mRNA and protein levels and the proteolytic activity of MMP-9 in HeLa and SiHa cells. sLZIP also increased the transcriptional activity of MMP-9 by binding directly to the cAMP-responsive element of the MMP-9 promoter region. Involvement of sLZIP in MMP-9 expression was further supported by the fact that ME-180 cells expressing sLZIP siRNA were refractory to MMP-9 expression. Results from wound healing and invasion assays showed that sLZIP enhanced both the migration and invasion of cervical cancer cells. The increased migration and invasion of HeLa and SiHa cells that were induced by sLZIP were abrogated by inhibition of the proteolytic activity of MMP-9. These results indicate that sLZIP plays a critical role in MMP-9 expression and is probably involved in invasion and metastasis of cervical cancer. Background: Proteolytic degradation of the extracellular matrix and basement membranes by matrix metalloproteinases (MMPs) is crucial in tumor invasion and metastasis. Results: sLZIP induces the expression of MMP-9, leading to enhancement of migration and invasion of cervical cancer cells. Conclusion: A novel regulatory mechanism of MMP-9 expression is characterized. Significance: sLZIP is a potential target for preventing the invasion and metastasis of cervical cancer.</description><subject>Cancer Biology</subject><subject>Cell Invasion</subject><subject>Cell Line, Tumor</subject><subject>Cell Migration</subject><subject>Cell Movement</subject><subject>Cervical Cancer</subject><subject>Cyclic AMP Response Element-Binding Protein - chemistry</subject><subject>Female</subject><subject>Gene Expression Regulation, Enzymologic</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>HeLa Cells</subject><subject>Humans</subject><subject>Matrix Metalloproteinase (MMP)</subject><subject>Matrix Metalloproteinase 9 - biosynthesis</subject><subject>Molecular Bases of Disease</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Metastasis</subject><subject>Promoter Regions, Genetic</subject><subject>Proteolysis</subject><subject>RNA Interference</subject><subject>sLZIP</subject><subject>Transcription Factors</subject><subject>Uterine Cervical Neoplasms - metabolism</subject><issn>0021-9258</issn><issn>1083-351X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp1kctu1DAUhi0EokNhzQ55xypT3zKON0hoVOhIM6KLLlA3lmOfFFcZO9hJVJ6A18ajtBUs8Mby8Xf-c_kRek_JmhIpLu5buz5QStdMMk7YC7SipOEVr-n3l2hFCKOVYnVzht7kfE_KEYq-RmeMEaJkTVbo99V0NAHvYbI-AL71wwAJX6c4gg84729313gX3GQh44O_S2b0MWATXInOJp8escNbSLO3psdbE2zJ30LfZzx7gy8fhgT5iTuYMfkHfIDR9H0cliomQ6Xeoled6TO8e7zP0c2Xy5vtVbX_9nW3_byvrBBsrNxGSQDKrZS12DAjiLGyA0I3YJkSgsvGWNbUru2I6RrXtlzJDbfcKS6Z4-fo0yI7TO0RnIUwJtPrIfmjSb90NF7_-xP8D30XZ80ZF0rSIvDxUSDFnxPkUR99tmVcEyBOWSvSSEGIJIW8WEibYs4JuucqlOiTebqYp0_m6cW8kvHh7-ae-Se3CqAWAMqGZg9JZ-uhbNz5BHbULvr_iv8B666reQ</recordid><startdate>20111209</startdate><enddate>20111209</enddate><creator>Kang, Hyereen</creator><creator>Jang, Sung-Wuk</creator><creator>Ko, Jesang</creator><general>Elsevier Inc</general><general>American Society for Biochemistry and Molecular Biology</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>20111209</creationdate><title>Human Leucine Zipper Protein sLZIP Induces Migration and Invasion of Cervical Cancer Cells via Expression of Matrix Metalloproteinase-9</title><author>Kang, Hyereen ; Jang, Sung-Wuk ; Ko, Jesang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c442t-d697ee13c775462a40ac7fe016ec2944378ac285dbf0af8dbb39763c3d9372d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Cancer Biology</topic><topic>Cell Invasion</topic><topic>Cell Line, Tumor</topic><topic>Cell Migration</topic><topic>Cell Movement</topic><topic>Cervical Cancer</topic><topic>Cyclic AMP Response Element-Binding Protein - chemistry</topic><topic>Female</topic><topic>Gene Expression Regulation, Enzymologic</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>HeLa Cells</topic><topic>Humans</topic><topic>Matrix Metalloproteinase (MMP)</topic><topic>Matrix Metalloproteinase 9 - biosynthesis</topic><topic>Molecular Bases of Disease</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Metastasis</topic><topic>Promoter Regions, Genetic</topic><topic>Proteolysis</topic><topic>RNA Interference</topic><topic>sLZIP</topic><topic>Transcription Factors</topic><topic>Uterine Cervical Neoplasms - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kang, Hyereen</creatorcontrib><creatorcontrib>Jang, Sung-Wuk</creatorcontrib><creatorcontrib>Ko, Jesang</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><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><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of biological chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kang, Hyereen</au><au>Jang, Sung-Wuk</au><au>Ko, Jesang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Human Leucine Zipper Protein sLZIP Induces Migration and Invasion of Cervical Cancer Cells via Expression of Matrix Metalloproteinase-9</atitle><jtitle>The Journal of biological chemistry</jtitle><addtitle>J Biol Chem</addtitle><date>2011-12-09</date><risdate>2011</risdate><volume>286</volume><issue>49</issue><spage>42072</spage><epage>42081</epage><pages>42072-42081</pages><issn>0021-9258</issn><eissn>1083-351X</eissn><abstract>Extracellular proteolysis mediates tissue homeostasis. In cancer, altered proteolysis leads to abnormal tumor growth, inflammation, tissue invasion, and metastasis. Matrix metalloproteinase-9 (MMP-9) represents one of the most prominent proteinases associated with inflammation and tumorigenesis. The recently identified human transcription factor sLZIP is a member of the leucine zipper transcription factor family. Although sLZIP is known to function in ligand-induced transactivation of the glucocorticoid receptor, its exact functions and target genes are not known. In this study, we investigated the role of sLZIP in MMP-9 expression and its involvement in cervical cancer development. Our results show that sLZIP increased the expression of MMP-9 at both the mRNA and protein levels and the proteolytic activity of MMP-9 in HeLa and SiHa cells. sLZIP also increased the transcriptional activity of MMP-9 by binding directly to the cAMP-responsive element of the MMP-9 promoter region. Involvement of sLZIP in MMP-9 expression was further supported by the fact that ME-180 cells expressing sLZIP siRNA were refractory to MMP-9 expression. Results from wound healing and invasion assays showed that sLZIP enhanced both the migration and invasion of cervical cancer cells. The increased migration and invasion of HeLa and SiHa cells that were induced by sLZIP were abrogated by inhibition of the proteolytic activity of MMP-9. These results indicate that sLZIP plays a critical role in MMP-9 expression and is probably involved in invasion and metastasis of cervical cancer. Background: Proteolytic degradation of the extracellular matrix and basement membranes by matrix metalloproteinases (MMPs) is crucial in tumor invasion and metastasis. Results: sLZIP induces the expression of MMP-9, leading to enhancement of migration and invasion of cervical cancer cells. Conclusion: A novel regulatory mechanism of MMP-9 expression is characterized. Significance: sLZIP is a potential target for preventing the invasion and metastasis of cervical cancer.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>22009750</pmid><doi>10.1074/jbc.M111.272302</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0021-9258
ispartof The Journal of biological chemistry, 2011-12, Vol.286 (49), p.42072-42081
issn 0021-9258
1083-351X
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3234971
source Open Access: PubMed Central; ScienceDirect®
subjects Cancer Biology
Cell Invasion
Cell Line, Tumor
Cell Migration
Cell Movement
Cervical Cancer
Cyclic AMP Response Element-Binding Protein - chemistry
Female
Gene Expression Regulation, Enzymologic
Gene Expression Regulation, Neoplastic
HeLa Cells
Humans
Matrix Metalloproteinase (MMP)
Matrix Metalloproteinase 9 - biosynthesis
Molecular Bases of Disease
Neoplasm Invasiveness
Neoplasm Metastasis
Promoter Regions, Genetic
Proteolysis
RNA Interference
sLZIP
Transcription Factors
Uterine Cervical Neoplasms - metabolism
title Human Leucine Zipper Protein sLZIP Induces Migration and Invasion of Cervical Cancer Cells via Expression of Matrix Metalloproteinase-9
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T23%3A15%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Human%20Leucine%20Zipper%20Protein%20sLZIP%20Induces%20Migration%20and%20Invasion%20of%20Cervical%20Cancer%20Cells%20via%20Expression%20of%20Matrix%20Metalloproteinase-9&rft.jtitle=The%20Journal%20of%20biological%20chemistry&rft.au=Kang,%20Hyereen&rft.date=2011-12-09&rft.volume=286&rft.issue=49&rft.spage=42072&rft.epage=42081&rft.pages=42072-42081&rft.issn=0021-9258&rft.eissn=1083-351X&rft_id=info:doi/10.1074/jbc.M111.272302&rft_dat=%3Cproquest_pubme%3E908740070%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c442t-d697ee13c775462a40ac7fe016ec2944378ac285dbf0af8dbb39763c3d9372d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=908740070&rft_id=info:pmid/22009750&rfr_iscdi=true