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Dykellic acid inhibits phorbol myristate acetate-induced matrix metalloproteinase-9 expression by inhibiting nuclear factor κB transcriptional activity
Proteolytic degradation of the extracellular matrix and tumor metastasis correlate with expression of endopeptidases known as matrix metalloproteinases (MMPs). Expression of MMPs is regulated by cytokines and signal transduction pathways, including those activated by phorbol myristate acetate. We fo...
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Published in: | Cancer research (Chicago, Ill.) Ill.), 2003-06, Vol.63 (12), p.3430-3434 |
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creator | WOO, Ju-Hyung PARK, Jong-Wook LEE, Sung-Hee KIM, Young-Ho IN KYU LEE GABRIELSON, Edward LEE, Sang-Han LEE, Ho-Jae KHO, Yung-Hee TAEG KYU KWON |
description | Proteolytic degradation of the extracellular matrix and tumor metastasis correlate with expression of endopeptidases known as matrix metalloproteinases (MMPs). Expression of MMPs is regulated by cytokines and signal transduction pathways, including those activated by phorbol myristate acetate. We found that dykellic acid, a fungal metabolite, significantly inhibits the phorbol myristate acetate-induced increase in MMP-9 expression and activity. These effects of dykellic acid are time- and dose-dependent, and correlate with decreased MMP-9 promoter activity and mRNA expression. Whereas this compound does not affect DNA binding activity of nuclear factor kappa B (NF kappa B), dykellic acid does inhibit transactivation of NF kappa B. These data demonstrate a role for NF kappa B in the regulation of MMP-9 expression and the ability of dykellic acid to suppress this action of NF kappa B. |
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Expression of MMPs is regulated by cytokines and signal transduction pathways, including those activated by phorbol myristate acetate. We found that dykellic acid, a fungal metabolite, significantly inhibits the phorbol myristate acetate-induced increase in MMP-9 expression and activity. These effects of dykellic acid are time- and dose-dependent, and correlate with decreased MMP-9 promoter activity and mRNA expression. Whereas this compound does not affect DNA binding activity of nuclear factor kappa B (NF kappa B), dykellic acid does inhibit transactivation of NF kappa B. These data demonstrate a role for NF kappa B in the regulation of MMP-9 expression and the ability of dykellic acid to suppress this action of NF kappa B.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 12810681</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Antineoplastic agents ; Biological and medical sciences ; Chemotherapy ; Enzyme Induction - drug effects ; Gene Expression Regulation, Neoplastic - drug effects ; Genes, Reporter ; Humans ; Luciferases - analysis ; Luciferases - genetics ; Matrix Metalloproteinase 2 - biosynthesis ; Matrix Metalloproteinase 2 - genetics ; Matrix Metalloproteinase 9 - biosynthesis ; Matrix Metalloproteinase 9 - genetics ; Medical sciences ; Neoplasm Invasiveness ; Neoplasm Proteins - antagonists & inhibitors ; Neoplasm Proteins - biosynthesis ; Neoplasm Proteins - chemistry ; Neoplasm Proteins - genetics ; NF-kappa B - antagonists & inhibitors ; NF-kappa B - chemistry ; NF-kappa B - physiology ; Pharmacology. Drug treatments ; Proline - analogs & derivatives ; Proline - pharmacology ; Promoter Regions, Genetic - drug effects ; Propionates - pharmacology ; Protein Structure, Tertiary ; Pyrones - pharmacology ; RNA, Messenger - biosynthesis ; RNA, Messenger - genetics ; Tetradecanoylphorbol Acetate - antagonists & inhibitors ; Tetradecanoylphorbol Acetate - pharmacology ; Thiocarbamates - pharmacology ; Thioctic Acid - pharmacology ; Transcription Factor AP-1 - metabolism ; Transcriptional Activation - drug effects ; Transfection ; Tumor Cells, Cultured - drug effects ; Tumor Cells, Cultured - enzymology</subject><ispartof>Cancer research (Chicago, Ill.), 2003-06, Vol.63 (12), p.3430-3434</ispartof><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14886232$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12810681$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WOO, Ju-Hyung</creatorcontrib><creatorcontrib>PARK, Jong-Wook</creatorcontrib><creatorcontrib>LEE, Sung-Hee</creatorcontrib><creatorcontrib>KIM, Young-Ho</creatorcontrib><creatorcontrib>IN KYU LEE</creatorcontrib><creatorcontrib>GABRIELSON, Edward</creatorcontrib><creatorcontrib>LEE, Sang-Han</creatorcontrib><creatorcontrib>LEE, Ho-Jae</creatorcontrib><creatorcontrib>KHO, Yung-Hee</creatorcontrib><creatorcontrib>TAEG KYU KWON</creatorcontrib><title>Dykellic acid inhibits phorbol myristate acetate-induced matrix metalloproteinase-9 expression by inhibiting nuclear factor κB transcriptional activity</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Proteolytic degradation of the extracellular matrix and tumor metastasis correlate with expression of endopeptidases known as matrix metalloproteinases (MMPs). Expression of MMPs is regulated by cytokines and signal transduction pathways, including those activated by phorbol myristate acetate. We found that dykellic acid, a fungal metabolite, significantly inhibits the phorbol myristate acetate-induced increase in MMP-9 expression and activity. These effects of dykellic acid are time- and dose-dependent, and correlate with decreased MMP-9 promoter activity and mRNA expression. Whereas this compound does not affect DNA binding activity of nuclear factor kappa B (NF kappa B), dykellic acid does inhibit transactivation of NF kappa B. These data demonstrate a role for NF kappa B in the regulation of MMP-9 expression and the ability of dykellic acid to suppress this action of NF kappa B.</description><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>Chemotherapy</subject><subject>Enzyme Induction - drug effects</subject><subject>Gene Expression Regulation, Neoplastic - drug effects</subject><subject>Genes, Reporter</subject><subject>Humans</subject><subject>Luciferases - analysis</subject><subject>Luciferases - genetics</subject><subject>Matrix Metalloproteinase 2 - biosynthesis</subject><subject>Matrix Metalloproteinase 2 - genetics</subject><subject>Matrix Metalloproteinase 9 - biosynthesis</subject><subject>Matrix Metalloproteinase 9 - genetics</subject><subject>Medical sciences</subject><subject>Neoplasm Invasiveness</subject><subject>Neoplasm Proteins - antagonists & inhibitors</subject><subject>Neoplasm Proteins - biosynthesis</subject><subject>Neoplasm Proteins - chemistry</subject><subject>Neoplasm Proteins - genetics</subject><subject>NF-kappa B - antagonists & inhibitors</subject><subject>NF-kappa B - chemistry</subject><subject>NF-kappa B - physiology</subject><subject>Pharmacology. Drug treatments</subject><subject>Proline - analogs & derivatives</subject><subject>Proline - pharmacology</subject><subject>Promoter Regions, Genetic - drug effects</subject><subject>Propionates - pharmacology</subject><subject>Protein Structure, Tertiary</subject><subject>Pyrones - pharmacology</subject><subject>RNA, Messenger - biosynthesis</subject><subject>RNA, Messenger - genetics</subject><subject>Tetradecanoylphorbol Acetate - antagonists & inhibitors</subject><subject>Tetradecanoylphorbol Acetate - pharmacology</subject><subject>Thiocarbamates - pharmacology</subject><subject>Thioctic Acid - pharmacology</subject><subject>Transcription Factor AP-1 - metabolism</subject><subject>Transcriptional Activation - drug effects</subject><subject>Transfection</subject><subject>Tumor Cells, Cultured - drug effects</subject><subject>Tumor Cells, Cultured - enzymology</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNpFkE1OAzEMhSMEoqVwBZQNy5GSSTJJl1B-pUpsuq88mQw1ZH6UpIi5CWfhEJyJIECsnmx_en72AZlzJUyhpVSHZM4YM4WSupyRkxifc6k4U8dkxkvDWWX4nLxfTy_Oe7QULDYU-x3WmCIdd0OoB0-7KWBMkFyeu28tsG_21jW0gxTwjXa56_0whiE57CG6Yknd2xhcjDj0tJ7-PLF_ov3eegeBtmDTEOjnxxVNAfpoA44p4-DzmoSvmKZTctSCj-7sVxdkc3uzWd0X68e7h9XluhhLoVOR72mkgyWXS90Y6ZRuDRguSilBc1eBkbzRurKirWplmCiVrZSqamDCaiYW5PzHdtzXnWu2Y8AOwrT9-1AGLn4BiBZ8m-NajP-cNKYqRSm-ADI1dNA</recordid><startdate>20030615</startdate><enddate>20030615</enddate><creator>WOO, Ju-Hyung</creator><creator>PARK, Jong-Wook</creator><creator>LEE, Sung-Hee</creator><creator>KIM, Young-Ho</creator><creator>IN KYU LEE</creator><creator>GABRIELSON, Edward</creator><creator>LEE, Sang-Han</creator><creator>LEE, Ho-Jae</creator><creator>KHO, Yung-Hee</creator><creator>TAEG KYU KWON</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20030615</creationdate><title>Dykellic acid inhibits phorbol myristate acetate-induced matrix metalloproteinase-9 expression by inhibiting nuclear factor κB transcriptional activity</title><author>WOO, Ju-Hyung ; PARK, Jong-Wook ; LEE, Sung-Hee ; KIM, Young-Ho ; IN KYU LEE ; GABRIELSON, Edward ; LEE, Sang-Han ; LEE, Ho-Jae ; KHO, Yung-Hee ; TAEG KYU KWON</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p237t-105d4ea91497d84e57f8a813244a71e6a841d776c3f6b580325c6556ba03c703</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>Chemotherapy</topic><topic>Enzyme Induction - drug effects</topic><topic>Gene Expression Regulation, Neoplastic - drug effects</topic><topic>Genes, Reporter</topic><topic>Humans</topic><topic>Luciferases - analysis</topic><topic>Luciferases - genetics</topic><topic>Matrix Metalloproteinase 2 - biosynthesis</topic><topic>Matrix Metalloproteinase 2 - genetics</topic><topic>Matrix Metalloproteinase 9 - biosynthesis</topic><topic>Matrix Metalloproteinase 9 - genetics</topic><topic>Medical sciences</topic><topic>Neoplasm Invasiveness</topic><topic>Neoplasm Proteins - antagonists & inhibitors</topic><topic>Neoplasm Proteins - biosynthesis</topic><topic>Neoplasm Proteins - chemistry</topic><topic>Neoplasm Proteins - genetics</topic><topic>NF-kappa B - antagonists & inhibitors</topic><topic>NF-kappa B - chemistry</topic><topic>NF-kappa B - physiology</topic><topic>Pharmacology. Drug treatments</topic><topic>Proline - analogs & derivatives</topic><topic>Proline - pharmacology</topic><topic>Promoter Regions, Genetic - drug effects</topic><topic>Propionates - pharmacology</topic><topic>Protein Structure, Tertiary</topic><topic>Pyrones - pharmacology</topic><topic>RNA, Messenger - biosynthesis</topic><topic>RNA, Messenger - genetics</topic><topic>Tetradecanoylphorbol Acetate - antagonists & inhibitors</topic><topic>Tetradecanoylphorbol Acetate - pharmacology</topic><topic>Thiocarbamates - pharmacology</topic><topic>Thioctic Acid - pharmacology</topic><topic>Transcription Factor AP-1 - metabolism</topic><topic>Transcriptional Activation - drug effects</topic><topic>Transfection</topic><topic>Tumor Cells, Cultured - drug effects</topic><topic>Tumor Cells, Cultured - enzymology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WOO, Ju-Hyung</creatorcontrib><creatorcontrib>PARK, Jong-Wook</creatorcontrib><creatorcontrib>LEE, Sung-Hee</creatorcontrib><creatorcontrib>KIM, Young-Ho</creatorcontrib><creatorcontrib>IN KYU LEE</creatorcontrib><creatorcontrib>GABRIELSON, Edward</creatorcontrib><creatorcontrib>LEE, Sang-Han</creatorcontrib><creatorcontrib>LEE, Ho-Jae</creatorcontrib><creatorcontrib>KHO, Yung-Hee</creatorcontrib><creatorcontrib>TAEG KYU KWON</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WOO, Ju-Hyung</au><au>PARK, Jong-Wook</au><au>LEE, Sung-Hee</au><au>KIM, Young-Ho</au><au>IN KYU LEE</au><au>GABRIELSON, Edward</au><au>LEE, Sang-Han</au><au>LEE, Ho-Jae</au><au>KHO, Yung-Hee</au><au>TAEG KYU KWON</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Dykellic acid inhibits phorbol myristate acetate-induced matrix metalloproteinase-9 expression by inhibiting nuclear factor κB transcriptional activity</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>2003-06-15</date><risdate>2003</risdate><volume>63</volume><issue>12</issue><spage>3430</spage><epage>3434</epage><pages>3430-3434</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Proteolytic degradation of the extracellular matrix and tumor metastasis correlate with expression of endopeptidases known as matrix metalloproteinases (MMPs). Expression of MMPs is regulated by cytokines and signal transduction pathways, including those activated by phorbol myristate acetate. We found that dykellic acid, a fungal metabolite, significantly inhibits the phorbol myristate acetate-induced increase in MMP-9 expression and activity. These effects of dykellic acid are time- and dose-dependent, and correlate with decreased MMP-9 promoter activity and mRNA expression. Whereas this compound does not affect DNA binding activity of nuclear factor kappa B (NF kappa B), dykellic acid does inhibit transactivation of NF kappa B. These data demonstrate a role for NF kappa B in the regulation of MMP-9 expression and the ability of dykellic acid to suppress this action of NF kappa B.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>12810681</pmid><tpages>5</tpages></addata></record> |
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subjects | Antineoplastic agents Biological and medical sciences Chemotherapy Enzyme Induction - drug effects Gene Expression Regulation, Neoplastic - drug effects Genes, Reporter Humans Luciferases - analysis Luciferases - genetics Matrix Metalloproteinase 2 - biosynthesis Matrix Metalloproteinase 2 - genetics Matrix Metalloproteinase 9 - biosynthesis Matrix Metalloproteinase 9 - genetics Medical sciences Neoplasm Invasiveness Neoplasm Proteins - antagonists & inhibitors Neoplasm Proteins - biosynthesis Neoplasm Proteins - chemistry Neoplasm Proteins - genetics NF-kappa B - antagonists & inhibitors NF-kappa B - chemistry NF-kappa B - physiology Pharmacology. Drug treatments Proline - analogs & derivatives Proline - pharmacology Promoter Regions, Genetic - drug effects Propionates - pharmacology Protein Structure, Tertiary Pyrones - pharmacology RNA, Messenger - biosynthesis RNA, Messenger - genetics Tetradecanoylphorbol Acetate - antagonists & inhibitors Tetradecanoylphorbol Acetate - pharmacology Thiocarbamates - pharmacology Thioctic Acid - pharmacology Transcription Factor AP-1 - metabolism Transcriptional Activation - drug effects Transfection Tumor Cells, Cultured - drug effects Tumor Cells, Cultured - enzymology |
title | Dykellic acid inhibits phorbol myristate acetate-induced matrix metalloproteinase-9 expression by inhibiting nuclear factor κB transcriptional activity |
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