Loading…
Anethole Exerts Antimetatstaic Activity via Inhibition of Matrix Metalloproteinase 2/9 and AKT/Mitogen-Activated Kinase/Nuclear Factor Kappa B Signaling Pathways
Anethole is known to possess anti-inflammatory and anti-tumor activities and to be a main constituent of fennel, anise, and camphor. In the present study, we evaluated anti-metastatic and apoptotic effects of anethole on highly-metastatic HT-1080 human fibrosarcoma tumor cells. Despite weak cytotoxi...
Saved in:
Published in: | Biological & Pharmaceutical Bulletin 2011/01/01, Vol.34(1), pp.41-46 |
---|---|
Main Authors: | , , , , , , , , , , , , , , |
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-c617t-eaa1ce4f1fa00b81708225591575f7dd7be2b18df3ff5fd2d50842f0c6108653 |
---|---|
cites | cdi_FETCH-LOGICAL-c617t-eaa1ce4f1fa00b81708225591575f7dd7be2b18df3ff5fd2d50842f0c6108653 |
container_end_page | 46 |
container_issue | 1 |
container_start_page | 41 |
container_title | Biological & Pharmaceutical Bulletin |
container_volume | 34 |
creator | Choo, Eun Jeong Rhee, Yun-Hee Jeong, Soo-Jin Lee, Hyo-Jung Kim, Hyun Seok Ko, Hyun Suk Kim, Ji-Hyun Kwon, Tae-Rin Jung, Ji Hoon Kim, Jin Hyoung Lee, Hyo-Jeong Lee, Eun-Ok Kim, Dae Keun Chen, Chang-Yan Kim, Sung-Hoon |
description | Anethole is known to possess anti-inflammatory and anti-tumor activities and to be a main constituent of fennel, anise, and camphor. In the present study, we evaluated anti-metastatic and apoptotic effects of anethole on highly-metastatic HT-1080 human fibrosarcoma tumor cells. Despite weak cytotoxicity against HT-1080 cells, anethole inhibited the adhesion to Matrigel and invasion of HT-1080 cells in a dose-dependent manner. Anethole was also able to down-regulate the expression of matrix metalloproteinase (MMP)-2 and -9 and up-regulate the gene expression of tissue inhibitor of metalloproteinase (TIMP)-1. The similar inhibitory effect of anethole on MMP-2 and -9 activities was confirmed by zymography assay. Furthermore, anethole significantly decreased mRNA expression of urokinase plasminogen activator (uPA), but not uPA receptor (uPAR). In addition, anethole suppressed the phosphorylation of AKT, extracellular signal-regulated kinase (ERK), p38 and nuclear transcription factor kappa B (NF-κB) in HT-1080 cells. Taken together, our findings indicate that anethole is a potent anti-metastatic drug that functions through inhibiting MMP-2/9 and AKT/mitogen-activated protein kinase (MAPK)/NF-κB signal transducers. |
doi_str_mv | 10.1248/bpb.34.41 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_822903985</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3121491701</sourcerecordid><originalsourceid>FETCH-LOGICAL-c617t-eaa1ce4f1fa00b81708225591575f7dd7be2b18df3ff5fd2d50842f0c6108653</originalsourceid><addsrcrecordid>eNpdkc9uEzEQxi0EomngwAsgSxwQh038N7t7QQpVW6o0gETu1qzXmzja2KntlOZx-qY4TVMkZHnGkn_zzdgfQh8oGVEmqnGzbUZcjAR9hQaUi7KQjMrXaEBqWhUTKqszdB7jmhBSEsbfojNG85JUDtDj1Jm08r3Blw8mpIinLtmNSZBiAqvxVCd7b9Me31vAN25lG5usd9h3eA4p2Ac8z3Df-23wyVgH0WA2rjG4Fk9ni_HcJr80rnjSgWRaPHuCxj92ujcQ8BXo5AOewXYL-Bv-bZcOeuuW-Bek1R_Yx3foTQd9NO-f8xAtri4XF9-L25_XNxfT20JPaJkKA0C1ER3tgJCmoiWpGJOyprKUXdm2ZWNYQ6u2410nu5a1klSCdSRXk2oi-RB9Psrmh9ztTExqY6M2fQ_O-F1UWa0mvK4O5Kf_yLXfhTx1VFSImpcVy3GIvhwpHXyMwXRqG-wGwl5Rog6uqeya4kIJmtmPz4q7ZmPaF_JkUwauj0C-tRp67_IXmX99dSwb63uvGKFUEcIFOaQyb3E4iAnldZY6jPX1qLTO_i7NSysIyWZDTkPRY8jFpwu9gqCM438B9NXAhg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1449378249</pqid></control><display><type>article</type><title>Anethole Exerts Antimetatstaic Activity via Inhibition of Matrix Metalloproteinase 2/9 and AKT/Mitogen-Activated Kinase/Nuclear Factor Kappa B Signaling Pathways</title><source>Free Full-Text Journals in Chemistry</source><creator>Choo, Eun Jeong ; Rhee, Yun-Hee ; Jeong, Soo-Jin ; Lee, Hyo-Jung ; Kim, Hyun Seok ; Ko, Hyun Suk ; Kim, Ji-Hyun ; Kwon, Tae-Rin ; Jung, Ji Hoon ; Kim, Jin Hyoung ; Lee, Hyo-Jeong ; Lee, Eun-Ok ; Kim, Dae Keun ; Chen, Chang-Yan ; Kim, Sung-Hoon</creator><creatorcontrib>Choo, Eun Jeong ; Rhee, Yun-Hee ; Jeong, Soo-Jin ; Lee, Hyo-Jung ; Kim, Hyun Seok ; Ko, Hyun Suk ; Kim, Ji-Hyun ; Kwon, Tae-Rin ; Jung, Ji Hoon ; Kim, Jin Hyoung ; Lee, Hyo-Jeong ; Lee, Eun-Ok ; Kim, Dae Keun ; Chen, Chang-Yan ; Kim, Sung-Hoon ; bYonsei University School of Medicine ; Harvard Medical School ; aCollege of Oriental Medicine ; Woosuk University ; dBeth Israel Deaconess Medical Center ; cCollege of Pharmacy ; Kyung Hee University</creatorcontrib><description>Anethole is known to possess anti-inflammatory and anti-tumor activities and to be a main constituent of fennel, anise, and camphor. In the present study, we evaluated anti-metastatic and apoptotic effects of anethole on highly-metastatic HT-1080 human fibrosarcoma tumor cells. Despite weak cytotoxicity against HT-1080 cells, anethole inhibited the adhesion to Matrigel and invasion of HT-1080 cells in a dose-dependent manner. Anethole was also able to down-regulate the expression of matrix metalloproteinase (MMP)-2 and -9 and up-regulate the gene expression of tissue inhibitor of metalloproteinase (TIMP)-1. The similar inhibitory effect of anethole on MMP-2 and -9 activities was confirmed by zymography assay. Furthermore, anethole significantly decreased mRNA expression of urokinase plasminogen activator (uPA), but not uPA receptor (uPAR). In addition, anethole suppressed the phosphorylation of AKT, extracellular signal-regulated kinase (ERK), p38 and nuclear transcription factor kappa B (NF-κB) in HT-1080 cells. Taken together, our findings indicate that anethole is a potent anti-metastatic drug that functions through inhibiting MMP-2/9 and AKT/mitogen-activated protein kinase (MAPK)/NF-κB signal transducers.</description><identifier>ISSN: 0918-6158</identifier><identifier>EISSN: 1347-5215</identifier><identifier>DOI: 10.1248/bpb.34.41</identifier><identifier>PMID: 21212515</identifier><language>eng</language><publisher>Japan: The Pharmaceutical Society of Japan</publisher><subject>AKT ; anethole ; Animals ; Anisoles - chemistry ; Anisoles - pharmacology ; antimetastasis ; Cell Line, Tumor ; Dose-Response Relationship, Drug ; Humans ; matrix metalloproteinase ; Matrix Metalloproteinase Inhibitors ; mitogen-activated kinase ; Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors ; Molecular Structure ; Neoplasm Metastasis - prevention & control ; NF-kappa B - antagonists & inhibitors ; nuclear transcription factor kappa B ; Proto-Oncogene Proteins c-akt - antagonists & inhibitors ; Signal Transduction</subject><ispartof>Biological and Pharmaceutical Bulletin, 2011/01/01, Vol.34(1), pp.41-46</ispartof><rights>2011 The Pharmaceutical Society of Japan</rights><rights>Copyright Japan Science and Technology Agency 2011</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c617t-eaa1ce4f1fa00b81708225591575f7dd7be2b18df3ff5fd2d50842f0c6108653</citedby><cites>FETCH-LOGICAL-c617t-eaa1ce4f1fa00b81708225591575f7dd7be2b18df3ff5fd2d50842f0c6108653</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4022,27922,27923,27924</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21212515$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Choo, Eun Jeong</creatorcontrib><creatorcontrib>Rhee, Yun-Hee</creatorcontrib><creatorcontrib>Jeong, Soo-Jin</creatorcontrib><creatorcontrib>Lee, Hyo-Jung</creatorcontrib><creatorcontrib>Kim, Hyun Seok</creatorcontrib><creatorcontrib>Ko, Hyun Suk</creatorcontrib><creatorcontrib>Kim, Ji-Hyun</creatorcontrib><creatorcontrib>Kwon, Tae-Rin</creatorcontrib><creatorcontrib>Jung, Ji Hoon</creatorcontrib><creatorcontrib>Kim, Jin Hyoung</creatorcontrib><creatorcontrib>Lee, Hyo-Jeong</creatorcontrib><creatorcontrib>Lee, Eun-Ok</creatorcontrib><creatorcontrib>Kim, Dae Keun</creatorcontrib><creatorcontrib>Chen, Chang-Yan</creatorcontrib><creatorcontrib>Kim, Sung-Hoon</creatorcontrib><creatorcontrib>bYonsei University School of Medicine</creatorcontrib><creatorcontrib>Harvard Medical School</creatorcontrib><creatorcontrib>aCollege of Oriental Medicine</creatorcontrib><creatorcontrib>Woosuk University</creatorcontrib><creatorcontrib>dBeth Israel Deaconess Medical Center</creatorcontrib><creatorcontrib>cCollege of Pharmacy</creatorcontrib><creatorcontrib>Kyung Hee University</creatorcontrib><title>Anethole Exerts Antimetatstaic Activity via Inhibition of Matrix Metalloproteinase 2/9 and AKT/Mitogen-Activated Kinase/Nuclear Factor Kappa B Signaling Pathways</title><title>Biological & Pharmaceutical Bulletin</title><addtitle>Biol Pharm Bull</addtitle><description>Anethole is known to possess anti-inflammatory and anti-tumor activities and to be a main constituent of fennel, anise, and camphor. In the present study, we evaluated anti-metastatic and apoptotic effects of anethole on highly-metastatic HT-1080 human fibrosarcoma tumor cells. Despite weak cytotoxicity against HT-1080 cells, anethole inhibited the adhesion to Matrigel and invasion of HT-1080 cells in a dose-dependent manner. Anethole was also able to down-regulate the expression of matrix metalloproteinase (MMP)-2 and -9 and up-regulate the gene expression of tissue inhibitor of metalloproteinase (TIMP)-1. The similar inhibitory effect of anethole on MMP-2 and -9 activities was confirmed by zymography assay. Furthermore, anethole significantly decreased mRNA expression of urokinase plasminogen activator (uPA), but not uPA receptor (uPAR). In addition, anethole suppressed the phosphorylation of AKT, extracellular signal-regulated kinase (ERK), p38 and nuclear transcription factor kappa B (NF-κB) in HT-1080 cells. Taken together, our findings indicate that anethole is a potent anti-metastatic drug that functions through inhibiting MMP-2/9 and AKT/mitogen-activated protein kinase (MAPK)/NF-κB signal transducers.</description><subject>AKT</subject><subject>anethole</subject><subject>Animals</subject><subject>Anisoles - chemistry</subject><subject>Anisoles - pharmacology</subject><subject>antimetastasis</subject><subject>Cell Line, Tumor</subject><subject>Dose-Response Relationship, Drug</subject><subject>Humans</subject><subject>matrix metalloproteinase</subject><subject>Matrix Metalloproteinase Inhibitors</subject><subject>mitogen-activated kinase</subject><subject>Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors</subject><subject>Molecular Structure</subject><subject>Neoplasm Metastasis - prevention & control</subject><subject>NF-kappa B - antagonists & inhibitors</subject><subject>nuclear transcription factor kappa B</subject><subject>Proto-Oncogene Proteins c-akt - antagonists & inhibitors</subject><subject>Signal Transduction</subject><issn>0918-6158</issn><issn>1347-5215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpdkc9uEzEQxi0EomngwAsgSxwQh038N7t7QQpVW6o0gETu1qzXmzja2KntlOZx-qY4TVMkZHnGkn_zzdgfQh8oGVEmqnGzbUZcjAR9hQaUi7KQjMrXaEBqWhUTKqszdB7jmhBSEsbfojNG85JUDtDj1Jm08r3Blw8mpIinLtmNSZBiAqvxVCd7b9Me31vAN25lG5usd9h3eA4p2Ac8z3Df-23wyVgH0WA2rjG4Fk9ni_HcJr80rnjSgWRaPHuCxj92ujcQ8BXo5AOewXYL-Bv-bZcOeuuW-Bek1R_Yx3foTQd9NO-f8xAtri4XF9-L25_XNxfT20JPaJkKA0C1ER3tgJCmoiWpGJOyprKUXdm2ZWNYQ6u2410nu5a1klSCdSRXk2oi-RB9Psrmh9ztTExqY6M2fQ_O-F1UWa0mvK4O5Kf_yLXfhTx1VFSImpcVy3GIvhwpHXyMwXRqG-wGwl5Rog6uqeya4kIJmtmPz4q7ZmPaF_JkUwauj0C-tRp67_IXmX99dSwb63uvGKFUEcIFOaQyb3E4iAnldZY6jPX1qLTO_i7NSysIyWZDTkPRY8jFpwu9gqCM438B9NXAhg</recordid><startdate>20110101</startdate><enddate>20110101</enddate><creator>Choo, Eun Jeong</creator><creator>Rhee, Yun-Hee</creator><creator>Jeong, Soo-Jin</creator><creator>Lee, Hyo-Jung</creator><creator>Kim, Hyun Seok</creator><creator>Ko, Hyun Suk</creator><creator>Kim, Ji-Hyun</creator><creator>Kwon, Tae-Rin</creator><creator>Jung, Ji Hoon</creator><creator>Kim, Jin Hyoung</creator><creator>Lee, Hyo-Jeong</creator><creator>Lee, Eun-Ok</creator><creator>Kim, Dae Keun</creator><creator>Chen, Chang-Yan</creator><creator>Kim, Sung-Hoon</creator><general>The Pharmaceutical Society of Japan</general><general>Pharmaceutical Society of Japan</general><general>Japan Science and Technology Agency</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>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20110101</creationdate><title>Anethole Exerts Antimetatstaic Activity via Inhibition of Matrix Metalloproteinase 2/9 and AKT/Mitogen-Activated Kinase/Nuclear Factor Kappa B Signaling Pathways</title><author>Choo, Eun Jeong ; Rhee, Yun-Hee ; Jeong, Soo-Jin ; Lee, Hyo-Jung ; Kim, Hyun Seok ; Ko, Hyun Suk ; Kim, Ji-Hyun ; Kwon, Tae-Rin ; Jung, Ji Hoon ; Kim, Jin Hyoung ; Lee, Hyo-Jeong ; Lee, Eun-Ok ; Kim, Dae Keun ; Chen, Chang-Yan ; Kim, Sung-Hoon</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c617t-eaa1ce4f1fa00b81708225591575f7dd7be2b18df3ff5fd2d50842f0c6108653</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>AKT</topic><topic>anethole</topic><topic>Animals</topic><topic>Anisoles - chemistry</topic><topic>Anisoles - pharmacology</topic><topic>antimetastasis</topic><topic>Cell Line, Tumor</topic><topic>Dose-Response Relationship, Drug</topic><topic>Humans</topic><topic>matrix metalloproteinase</topic><topic>Matrix Metalloproteinase Inhibitors</topic><topic>mitogen-activated kinase</topic><topic>Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors</topic><topic>Molecular Structure</topic><topic>Neoplasm Metastasis - prevention & control</topic><topic>NF-kappa B - antagonists & inhibitors</topic><topic>nuclear transcription factor kappa B</topic><topic>Proto-Oncogene Proteins c-akt - antagonists & inhibitors</topic><topic>Signal Transduction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choo, Eun Jeong</creatorcontrib><creatorcontrib>Rhee, Yun-Hee</creatorcontrib><creatorcontrib>Jeong, Soo-Jin</creatorcontrib><creatorcontrib>Lee, Hyo-Jung</creatorcontrib><creatorcontrib>Kim, Hyun Seok</creatorcontrib><creatorcontrib>Ko, Hyun Suk</creatorcontrib><creatorcontrib>Kim, Ji-Hyun</creatorcontrib><creatorcontrib>Kwon, Tae-Rin</creatorcontrib><creatorcontrib>Jung, Ji Hoon</creatorcontrib><creatorcontrib>Kim, Jin Hyoung</creatorcontrib><creatorcontrib>Lee, Hyo-Jeong</creatorcontrib><creatorcontrib>Lee, Eun-Ok</creatorcontrib><creatorcontrib>Kim, Dae Keun</creatorcontrib><creatorcontrib>Chen, Chang-Yan</creatorcontrib><creatorcontrib>Kim, Sung-Hoon</creatorcontrib><creatorcontrib>bYonsei University School of Medicine</creatorcontrib><creatorcontrib>Harvard Medical School</creatorcontrib><creatorcontrib>aCollege of Oriental Medicine</creatorcontrib><creatorcontrib>Woosuk University</creatorcontrib><creatorcontrib>dBeth Israel Deaconess Medical Center</creatorcontrib><creatorcontrib>cCollege of Pharmacy</creatorcontrib><creatorcontrib>Kyung Hee University</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Biological & Pharmaceutical Bulletin</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choo, Eun Jeong</au><au>Rhee, Yun-Hee</au><au>Jeong, Soo-Jin</au><au>Lee, Hyo-Jung</au><au>Kim, Hyun Seok</au><au>Ko, Hyun Suk</au><au>Kim, Ji-Hyun</au><au>Kwon, Tae-Rin</au><au>Jung, Ji Hoon</au><au>Kim, Jin Hyoung</au><au>Lee, Hyo-Jeong</au><au>Lee, Eun-Ok</au><au>Kim, Dae Keun</au><au>Chen, Chang-Yan</au><au>Kim, Sung-Hoon</au><aucorp>bYonsei University School of Medicine</aucorp><aucorp>Harvard Medical School</aucorp><aucorp>aCollege of Oriental Medicine</aucorp><aucorp>Woosuk University</aucorp><aucorp>dBeth Israel Deaconess Medical Center</aucorp><aucorp>cCollege of Pharmacy</aucorp><aucorp>Kyung Hee University</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anethole Exerts Antimetatstaic Activity via Inhibition of Matrix Metalloproteinase 2/9 and AKT/Mitogen-Activated Kinase/Nuclear Factor Kappa B Signaling Pathways</atitle><jtitle>Biological & Pharmaceutical Bulletin</jtitle><addtitle>Biol Pharm Bull</addtitle><date>2011-01-01</date><risdate>2011</risdate><volume>34</volume><issue>1</issue><spage>41</spage><epage>46</epage><pages>41-46</pages><issn>0918-6158</issn><eissn>1347-5215</eissn><abstract>Anethole is known to possess anti-inflammatory and anti-tumor activities and to be a main constituent of fennel, anise, and camphor. In the present study, we evaluated anti-metastatic and apoptotic effects of anethole on highly-metastatic HT-1080 human fibrosarcoma tumor cells. Despite weak cytotoxicity against HT-1080 cells, anethole inhibited the adhesion to Matrigel and invasion of HT-1080 cells in a dose-dependent manner. Anethole was also able to down-regulate the expression of matrix metalloproteinase (MMP)-2 and -9 and up-regulate the gene expression of tissue inhibitor of metalloproteinase (TIMP)-1. The similar inhibitory effect of anethole on MMP-2 and -9 activities was confirmed by zymography assay. Furthermore, anethole significantly decreased mRNA expression of urokinase plasminogen activator (uPA), but not uPA receptor (uPAR). In addition, anethole suppressed the phosphorylation of AKT, extracellular signal-regulated kinase (ERK), p38 and nuclear transcription factor kappa B (NF-κB) in HT-1080 cells. Taken together, our findings indicate that anethole is a potent anti-metastatic drug that functions through inhibiting MMP-2/9 and AKT/mitogen-activated protein kinase (MAPK)/NF-κB signal transducers.</abstract><cop>Japan</cop><pub>The Pharmaceutical Society of Japan</pub><pmid>21212515</pmid><doi>10.1248/bpb.34.41</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0918-6158 |
ispartof | Biological and Pharmaceutical Bulletin, 2011/01/01, Vol.34(1), pp.41-46 |
issn | 0918-6158 1347-5215 |
language | eng |
recordid | cdi_proquest_miscellaneous_822903985 |
source | Free Full-Text Journals in Chemistry |
subjects | AKT anethole Animals Anisoles - chemistry Anisoles - pharmacology antimetastasis Cell Line, Tumor Dose-Response Relationship, Drug Humans matrix metalloproteinase Matrix Metalloproteinase Inhibitors mitogen-activated kinase Mitogen-Activated Protein Kinase Kinases - antagonists & inhibitors Molecular Structure Neoplasm Metastasis - prevention & control NF-kappa B - antagonists & inhibitors nuclear transcription factor kappa B Proto-Oncogene Proteins c-akt - antagonists & inhibitors Signal Transduction |
title | Anethole Exerts Antimetatstaic Activity via Inhibition of Matrix Metalloproteinase 2/9 and AKT/Mitogen-Activated Kinase/Nuclear Factor Kappa B Signaling Pathways |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T02%3A32%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Anethole%20Exerts%20Antimetatstaic%20Activity%20via%20Inhibition%20of%20Matrix%20Metalloproteinase%202/9%20and%20AKT/Mitogen-Activated%20Kinase/Nuclear%20Factor%20Kappa%20B%20Signaling%20Pathways&rft.jtitle=Biological%20&%20Pharmaceutical%20Bulletin&rft.au=Choo,%20Eun%20Jeong&rft.aucorp=bYonsei%20University%20School%20of%20Medicine&rft.date=2011-01-01&rft.volume=34&rft.issue=1&rft.spage=41&rft.epage=46&rft.pages=41-46&rft.issn=0918-6158&rft.eissn=1347-5215&rft_id=info:doi/10.1248/bpb.34.41&rft_dat=%3Cproquest_cross%3E3121491701%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c617t-eaa1ce4f1fa00b81708225591575f7dd7be2b18df3ff5fd2d50842f0c6108653%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1449378249&rft_id=info:pmid/21212515&rfr_iscdi=true |