Esculetin exerts anti-proliferative effects against non-small-cell lung carcinoma by suppressing specificity protein 1 in vitro
Esculetin, a coumarin derivative, is a phenolic compound isolated from Artemisia capillaris, Citrus limonia, and Euphorbia lathyris. Although it has been reported to have anti-inflammatory, anti-oxidant, and anti-proliferative activities in several human cancers, its anti-proliferative activity agai...
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Veröffentlicht in: | General physiology and biophysics 2017-01, Vol.36 (1), p.31-39 |
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creator | Lee, Ra H Jeon, Young-Joo Cho, Jin H Jang, Jeong-Yun Kong, Il-Keun Kim, Seok-Ho Kim, MinSeok S Chung, Hak-Jae Oh, Keon B Park, Seon-Min Shin, Jae-Cheon Seo, Jae-Min Ko, Sungho Shim, Jung-Hyun Chae, Jung-Il |
description | Esculetin, a coumarin derivative, is a phenolic compound isolated from Artemisia capillaris, Citrus limonia, and Euphorbia lathyris. Although it has been reported to have anti-inflammatory, anti-oxidant, and anti-proliferative activities in several human cancers, its anti-proliferative activity against non-small-cell lung carcinoma (NSCLC) and the molecular mechanisms involved have not been adequately elucidated. In this study, we used two NSCLC cell lines (NCI-H358 and NCI-H1299) to investigate the anti-proliferative activity and apoptotic effect of esculetin. Our data showed that esculetin-treated cells exhibited reduced proliferation and apoptotic cell morphologies. Intriguingly, the transcription factor specificity protein 1 (Sp1) was significantly suppressed by esculetin in a dose- and time-dependent manner. Furthermore, the levels of p27 and p21, two key regulators of the cell cycle, were up-regulated by the esculetin-mediated down-regulation of Sp1; the level of a third cell-cycle regulator, survivin, was decreased, resulting in caspase-dependent apoptosis. Therefore, we conclude that esculetin could be a potent anti-proliferative agent in patients with NSCLC. |
doi_str_mv | 10.4149/gpb_2016024 |
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Although it has been reported to have anti-inflammatory, anti-oxidant, and anti-proliferative activities in several human cancers, its anti-proliferative activity against non-small-cell lung carcinoma (NSCLC) and the molecular mechanisms involved have not been adequately elucidated. In this study, we used two NSCLC cell lines (NCI-H358 and NCI-H1299) to investigate the anti-proliferative activity and apoptotic effect of esculetin. Our data showed that esculetin-treated cells exhibited reduced proliferation and apoptotic cell morphologies. Intriguingly, the transcription factor specificity protein 1 (Sp1) was significantly suppressed by esculetin in a dose- and time-dependent manner. Furthermore, the levels of p27 and p21, two key regulators of the cell cycle, were up-regulated by the esculetin-mediated down-regulation of Sp1; the level of a third cell-cycle regulator, survivin, was decreased, resulting in caspase-dependent apoptosis. Therefore, we conclude that esculetin could be a potent anti-proliferative agent in patients with NSCLC.</description><identifier>ISSN: 0231-5882</identifier><identifier>ISSN: 1338-4325</identifier><identifier>EISSN: 1338-4325</identifier><identifier>DOI: 10.4149/gpb_2016024</identifier><identifier>PMID: 27901471</identifier><language>eng</language><publisher>Slovakia</publisher><subject>Antineoplastic Agents - pharmacology ; Antioxidants - pharmacology ; Carcinoma, Non-Small-Cell Lung - drug therapy ; Carcinoma, Non-Small-Cell Lung - metabolism ; Carcinoma, Non-Small-Cell Lung - pathology ; Cell Proliferation - drug effects ; Dose-Response Relationship, Drug ; Down-Regulation - drug effects ; Lung Neoplasms - drug therapy ; Lung Neoplasms - metabolism ; Lung Neoplasms - pathology ; Sp1 Transcription Factor - metabolism ; Umbelliferones - pharmacology</subject><ispartof>General physiology and biophysics, 2017-01, Vol.36 (1), p.31-39</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c326t-8f3b148c88972dbd284bac9a5e12809f5939d72affb2bedf1da1ee2627bf9da23</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27901471$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Ra H</creatorcontrib><creatorcontrib>Jeon, Young-Joo</creatorcontrib><creatorcontrib>Cho, Jin H</creatorcontrib><creatorcontrib>Jang, Jeong-Yun</creatorcontrib><creatorcontrib>Kong, Il-Keun</creatorcontrib><creatorcontrib>Kim, Seok-Ho</creatorcontrib><creatorcontrib>Kim, MinSeok S</creatorcontrib><creatorcontrib>Chung, Hak-Jae</creatorcontrib><creatorcontrib>Oh, Keon B</creatorcontrib><creatorcontrib>Park, Seon-Min</creatorcontrib><creatorcontrib>Shin, Jae-Cheon</creatorcontrib><creatorcontrib>Seo, Jae-Min</creatorcontrib><creatorcontrib>Ko, Sungho</creatorcontrib><creatorcontrib>Shim, Jung-Hyun</creatorcontrib><creatorcontrib>Chae, Jung-Il</creatorcontrib><title>Esculetin exerts anti-proliferative effects against non-small-cell lung carcinoma by suppressing specificity protein 1 in vitro</title><title>General physiology and biophysics</title><addtitle>Gen Physiol Biophys</addtitle><description>Esculetin, a coumarin derivative, is a phenolic compound isolated from Artemisia capillaris, Citrus limonia, and Euphorbia lathyris. Although it has been reported to have anti-inflammatory, anti-oxidant, and anti-proliferative activities in several human cancers, its anti-proliferative activity against non-small-cell lung carcinoma (NSCLC) and the molecular mechanisms involved have not been adequately elucidated. In this study, we used two NSCLC cell lines (NCI-H358 and NCI-H1299) to investigate the anti-proliferative activity and apoptotic effect of esculetin. Our data showed that esculetin-treated cells exhibited reduced proliferation and apoptotic cell morphologies. Intriguingly, the transcription factor specificity protein 1 (Sp1) was significantly suppressed by esculetin in a dose- and time-dependent manner. Furthermore, the levels of p27 and p21, two key regulators of the cell cycle, were up-regulated by the esculetin-mediated down-regulation of Sp1; the level of a third cell-cycle regulator, survivin, was decreased, resulting in caspase-dependent apoptosis. Therefore, we conclude that esculetin could be a potent anti-proliferative agent in patients with NSCLC.</description><subject>Antineoplastic Agents - pharmacology</subject><subject>Antioxidants - pharmacology</subject><subject>Carcinoma, Non-Small-Cell Lung - drug therapy</subject><subject>Carcinoma, Non-Small-Cell Lung - metabolism</subject><subject>Carcinoma, Non-Small-Cell Lung - pathology</subject><subject>Cell Proliferation - drug effects</subject><subject>Dose-Response Relationship, Drug</subject><subject>Down-Regulation - drug effects</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - pathology</subject><subject>Sp1 Transcription Factor - metabolism</subject><subject>Umbelliferones - pharmacology</subject><issn>0231-5882</issn><issn>1338-4325</issn><issn>1338-4325</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkE1LAzEQhoMottSevEvusppMdrvJUUr9gIIXPS9JdlIi-0WSLfbkX3dLVZzDzOF9eAceQq45u8t5ru53g6mA8RWD_IzMuRAyywUU52TOQPCskBJmZBnjB5umKBUAuyQzKBXjecnn5GsT7dhg8h3FTwwpUt0lnw2hb7zDoJPfI0Xn0B6jnfZdTLTruyy2umkyi01Dm7HbUauD9V3famoONI7DEDBGPwVxQOudtz4d6FSbcHrF6bT2PoX-ilw43URc_twFeX_cvK2fs-3r08v6YZtZAauUSScMz6WVUpVQmxpkbrRVukAOkilXKKHqErRzBgzWjteaI8IKSuNUrUEsyO2p14Y-xoCuGoJvdThUnFVHk9U_kxN9c6KH0bRY_7G_3sQ34yZyxg</recordid><startdate>201701</startdate><enddate>201701</enddate><creator>Lee, Ra H</creator><creator>Jeon, Young-Joo</creator><creator>Cho, Jin H</creator><creator>Jang, Jeong-Yun</creator><creator>Kong, Il-Keun</creator><creator>Kim, Seok-Ho</creator><creator>Kim, MinSeok S</creator><creator>Chung, Hak-Jae</creator><creator>Oh, Keon B</creator><creator>Park, Seon-Min</creator><creator>Shin, Jae-Cheon</creator><creator>Seo, Jae-Min</creator><creator>Ko, Sungho</creator><creator>Shim, Jung-Hyun</creator><creator>Chae, Jung-Il</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201701</creationdate><title>Esculetin exerts anti-proliferative effects against non-small-cell lung carcinoma by suppressing specificity protein 1 in vitro</title><author>Lee, Ra H ; Jeon, Young-Joo ; Cho, Jin H ; Jang, Jeong-Yun ; Kong, Il-Keun ; Kim, Seok-Ho ; Kim, MinSeok S ; Chung, Hak-Jae ; Oh, Keon B ; Park, Seon-Min ; Shin, Jae-Cheon ; Seo, Jae-Min ; Ko, Sungho ; Shim, Jung-Hyun ; Chae, Jung-Il</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-8f3b148c88972dbd284bac9a5e12809f5939d72affb2bedf1da1ee2627bf9da23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antineoplastic Agents - pharmacology</topic><topic>Antioxidants - pharmacology</topic><topic>Carcinoma, Non-Small-Cell Lung - drug therapy</topic><topic>Carcinoma, Non-Small-Cell Lung - metabolism</topic><topic>Carcinoma, Non-Small-Cell Lung - pathology</topic><topic>Cell Proliferation - drug effects</topic><topic>Dose-Response Relationship, Drug</topic><topic>Down-Regulation - drug effects</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lung Neoplasms - pathology</topic><topic>Sp1 Transcription Factor - metabolism</topic><topic>Umbelliferones - pharmacology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Ra H</creatorcontrib><creatorcontrib>Jeon, Young-Joo</creatorcontrib><creatorcontrib>Cho, Jin H</creatorcontrib><creatorcontrib>Jang, Jeong-Yun</creatorcontrib><creatorcontrib>Kong, Il-Keun</creatorcontrib><creatorcontrib>Kim, Seok-Ho</creatorcontrib><creatorcontrib>Kim, MinSeok S</creatorcontrib><creatorcontrib>Chung, Hak-Jae</creatorcontrib><creatorcontrib>Oh, Keon B</creatorcontrib><creatorcontrib>Park, Seon-Min</creatorcontrib><creatorcontrib>Shin, Jae-Cheon</creatorcontrib><creatorcontrib>Seo, Jae-Min</creatorcontrib><creatorcontrib>Ko, Sungho</creatorcontrib><creatorcontrib>Shim, Jung-Hyun</creatorcontrib><creatorcontrib>Chae, Jung-Il</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>General physiology and biophysics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Ra H</au><au>Jeon, Young-Joo</au><au>Cho, Jin H</au><au>Jang, Jeong-Yun</au><au>Kong, Il-Keun</au><au>Kim, Seok-Ho</au><au>Kim, MinSeok S</au><au>Chung, Hak-Jae</au><au>Oh, Keon B</au><au>Park, Seon-Min</au><au>Shin, Jae-Cheon</au><au>Seo, Jae-Min</au><au>Ko, Sungho</au><au>Shim, Jung-Hyun</au><au>Chae, Jung-Il</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Esculetin exerts anti-proliferative effects against non-small-cell lung carcinoma by suppressing specificity protein 1 in vitro</atitle><jtitle>General physiology and biophysics</jtitle><addtitle>Gen Physiol Biophys</addtitle><date>2017-01</date><risdate>2017</risdate><volume>36</volume><issue>1</issue><spage>31</spage><epage>39</epage><pages>31-39</pages><issn>0231-5882</issn><issn>1338-4325</issn><eissn>1338-4325</eissn><abstract>Esculetin, a coumarin derivative, is a phenolic compound isolated from Artemisia capillaris, Citrus limonia, and Euphorbia lathyris. Although it has been reported to have anti-inflammatory, anti-oxidant, and anti-proliferative activities in several human cancers, its anti-proliferative activity against non-small-cell lung carcinoma (NSCLC) and the molecular mechanisms involved have not been adequately elucidated. In this study, we used two NSCLC cell lines (NCI-H358 and NCI-H1299) to investigate the anti-proliferative activity and apoptotic effect of esculetin. Our data showed that esculetin-treated cells exhibited reduced proliferation and apoptotic cell morphologies. Intriguingly, the transcription factor specificity protein 1 (Sp1) was significantly suppressed by esculetin in a dose- and time-dependent manner. Furthermore, the levels of p27 and p21, two key regulators of the cell cycle, were up-regulated by the esculetin-mediated down-regulation of Sp1; the level of a third cell-cycle regulator, survivin, was decreased, resulting in caspase-dependent apoptosis. Therefore, we conclude that esculetin could be a potent anti-proliferative agent in patients with NSCLC.</abstract><cop>Slovakia</cop><pmid>27901471</pmid><doi>10.4149/gpb_2016024</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Antineoplastic Agents - pharmacology Antioxidants - pharmacology Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - metabolism Carcinoma, Non-Small-Cell Lung - pathology Cell Proliferation - drug effects Dose-Response Relationship, Drug Down-Regulation - drug effects Lung Neoplasms - drug therapy Lung Neoplasms - metabolism Lung Neoplasms - pathology Sp1 Transcription Factor - metabolism Umbelliferones - pharmacology |
title | Esculetin exerts anti-proliferative effects against non-small-cell lung carcinoma by suppressing specificity protein 1 in vitro |
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