Tumor-Inhibitory Effects of Zerumbone Against HT-29 Human Colorectal Cancer Cells
Colorectal cancer (CRC) is the second cause of cancer-associated death globally. Recently, herbal medicinal products and, in particular, zerumbone have been widely studied and used for cancer treatment as they induce significant anti-cancer effects. However, there is limited information about the an...
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Veröffentlicht in: | International journal of toxicology 2022-09, Vol.41 (5), p.402-411 |
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description | Colorectal cancer (CRC) is the second cause of cancer-associated death globally. Recently, herbal medicinal products and, in particular, zerumbone have been widely studied and used for cancer treatment as they induce significant anti-cancer effects. However, there is limited information about the anti-cancer effects of zerumbone in CRC. Therefore, we aimed to investigate the in vitro anti-cancer effects of the zerumbone in CRC, focusing on cell apoptosis and migration. Anti-proliferative and anti-migratory effects of zerumbone on HT-29 cells were evaluated using MTT and scratch wound healing assay, respectively. Quantitative real-time PCR (qRT-PCR) was performed to determine the mRNA expression levels of migration and apoptosis-related genes. Apoptosis and cell cycle distribution were evaluated by flow cytometry. The intracellular level of reactive oxygen species (ROS) was measured using a ROS assay kit. Additionally, matrix metalloproteinase-2/-9 (MMP-2/-9) activity was determined using gelatin zymography. Zerumbone suppressed the viability of the HT-29 cells dose-dependently while having less cytotoxicity on normal NIH/3T3 cells. Zerumbone induced apoptosis in HT-29 cells and arrested the cell cycle in the G2/M phase. These effects were associated with alteration in the expression of apoptosis-related genes (up-regulation of Bax and down-regulation of Bcl-2 genes). Zerumbone also enhanced the generation of ROS in HT-29 cells. Furthermore, zerumbone significantly inhibited the migration of HT-29 cells and decreased MMP-2/-9 mRNA expression and activity. Our findings provide a potential use for zerumbone to induce apoptosis and suppress metastasis in HT-29 cells; thus, it could be developed as a promising natural agent for future CRC therapy. |
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Recently, herbal medicinal products and, in particular, zerumbone have been widely studied and used for cancer treatment as they induce significant anti-cancer effects. However, there is limited information about the anti-cancer effects of zerumbone in CRC. Therefore, we aimed to investigate the in vitro anti-cancer effects of the zerumbone in CRC, focusing on cell apoptosis and migration. Anti-proliferative and anti-migratory effects of zerumbone on HT-29 cells were evaluated using MTT and scratch wound healing assay, respectively. Quantitative real-time PCR (qRT-PCR) was performed to determine the mRNA expression levels of migration and apoptosis-related genes. Apoptosis and cell cycle distribution were evaluated by flow cytometry. The intracellular level of reactive oxygen species (ROS) was measured using a ROS assay kit. Additionally, matrix metalloproteinase-2/-9 (MMP-2/-9) activity was determined using gelatin zymography. Zerumbone suppressed the viability of the HT-29 cells dose-dependently while having less cytotoxicity on normal NIH/3T3 cells. Zerumbone induced apoptosis in HT-29 cells and arrested the cell cycle in the G2/M phase. These effects were associated with alteration in the expression of apoptosis-related genes (up-regulation of Bax and down-regulation of Bcl-2 genes). Zerumbone also enhanced the generation of ROS in HT-29 cells. Furthermore, zerumbone significantly inhibited the migration of HT-29 cells and decreased MMP-2/-9 mRNA expression and activity. Our findings provide a potential use for zerumbone to induce apoptosis and suppress metastasis in HT-29 cells; thus, it could be developed as a promising natural agent for future CRC therapy.</description><identifier>ISSN: 1091-5818</identifier><identifier>EISSN: 1092-874X</identifier><identifier>DOI: 10.1177/10915818221104417</identifier><identifier>PMID: 35719111</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Animals ; Apoptosis ; Cell Line, Tumor ; Cell Proliferation ; Colorectal Neoplasms - drug therapy ; Colorectal Neoplasms - genetics ; Colorectal Neoplasms - metabolism ; HT29 Cells ; Humans ; Matrix Metalloproteinase 2 - pharmacology ; Mice ; Reactive Oxygen Species - metabolism ; RNA, Messenger ; Sesquiterpenes</subject><ispartof>International journal of toxicology, 2022-09, Vol.41 (5), p.402-411</ispartof><rights>The Author(s) 2022</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c270t-dc601104c87a5765b8e1bbe7d8f00d5db703c46548c151ccc6ed1f3063d72faa3</citedby><cites>FETCH-LOGICAL-c270t-dc601104c87a5765b8e1bbe7d8f00d5db703c46548c151ccc6ed1f3063d72faa3</cites><orcidid>0000-0001-7201-4178</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/10915818221104417$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/10915818221104417$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21818,27923,27924,43620,43621</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35719111$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Memari, Fezzeh</creatorcontrib><creatorcontrib>Mirzavi, Farshad</creatorcontrib><creatorcontrib>Jalili‐Nik, Mohammad</creatorcontrib><creatorcontrib>Afshari, Amir R.</creatorcontrib><creatorcontrib>Ghorbani, Ahmad</creatorcontrib><creatorcontrib>Soukhtanloo, Mohammad</creatorcontrib><title>Tumor-Inhibitory Effects of Zerumbone Against HT-29 Human Colorectal Cancer Cells</title><title>International journal of toxicology</title><addtitle>Int J Toxicol</addtitle><description>Colorectal cancer (CRC) is the second cause of cancer-associated death globally. Recently, herbal medicinal products and, in particular, zerumbone have been widely studied and used for cancer treatment as they induce significant anti-cancer effects. However, there is limited information about the anti-cancer effects of zerumbone in CRC. Therefore, we aimed to investigate the in vitro anti-cancer effects of the zerumbone in CRC, focusing on cell apoptosis and migration. Anti-proliferative and anti-migratory effects of zerumbone on HT-29 cells were evaluated using MTT and scratch wound healing assay, respectively. Quantitative real-time PCR (qRT-PCR) was performed to determine the mRNA expression levels of migration and apoptosis-related genes. Apoptosis and cell cycle distribution were evaluated by flow cytometry. The intracellular level of reactive oxygen species (ROS) was measured using a ROS assay kit. Additionally, matrix metalloproteinase-2/-9 (MMP-2/-9) activity was determined using gelatin zymography. Zerumbone suppressed the viability of the HT-29 cells dose-dependently while having less cytotoxicity on normal NIH/3T3 cells. Zerumbone induced apoptosis in HT-29 cells and arrested the cell cycle in the G2/M phase. These effects were associated with alteration in the expression of apoptosis-related genes (up-regulation of Bax and down-regulation of Bcl-2 genes). Zerumbone also enhanced the generation of ROS in HT-29 cells. Furthermore, zerumbone significantly inhibited the migration of HT-29 cells and decreased MMP-2/-9 mRNA expression and activity. Our findings provide a potential use for zerumbone to induce apoptosis and suppress metastasis in HT-29 cells; thus, it could be developed as a promising natural agent for future CRC therapy.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Cell Line, Tumor</subject><subject>Cell Proliferation</subject><subject>Colorectal Neoplasms - drug therapy</subject><subject>Colorectal Neoplasms - genetics</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>HT29 Cells</subject><subject>Humans</subject><subject>Matrix Metalloproteinase 2 - pharmacology</subject><subject>Mice</subject><subject>Reactive Oxygen Species - metabolism</subject><subject>RNA, Messenger</subject><subject>Sesquiterpenes</subject><issn>1091-5818</issn><issn>1092-874X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE9Lw0AQxRdRbK1-AC-yRy-pO5tsNj2WUG2hIEIF8RI2-6emJNm6mxz67d3Y6kXwNMPwe483D6FbIFMAzh-AzIBlkFEKQJIE-BkahxuNMp68nX_vEA3ACF15vyOEpJzBJRrFjMMMAMboZdM31kWr9qMqq866A14Yo2XnsTX4Xbu-KW2r8XwrqtZ3eLmJ6Awv-0a0OLe1dQEVNc5FK7XDua5rf40ujKi9vjnNCXp9XGzyZbR-flrl83UkKSddpGRKhtQy44LxlJWZhrLUXGWGEMVUyUksk5QlmQQGUspUKzAxSWPFqREinqD7o-_e2c9e-65oKi9DAtFq2_uCpjzUwCiwgMIRlc5677Qp9q5qhDsUQIqhyeJPk0Fzd7Lvy0arX8VPdQGYHgEvtrrY2d614d1_HL8AlFl58A</recordid><startdate>202209</startdate><enddate>202209</enddate><creator>Memari, Fezzeh</creator><creator>Mirzavi, Farshad</creator><creator>Jalili‐Nik, Mohammad</creator><creator>Afshari, Amir R.</creator><creator>Ghorbani, Ahmad</creator><creator>Soukhtanloo, Mohammad</creator><general>SAGE Publications</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>7X8</scope><orcidid>https://orcid.org/0000-0001-7201-4178</orcidid></search><sort><creationdate>202209</creationdate><title>Tumor-Inhibitory Effects of Zerumbone Against HT-29 Human Colorectal Cancer Cells</title><author>Memari, Fezzeh ; Mirzavi, Farshad ; Jalili‐Nik, Mohammad ; Afshari, Amir R. ; Ghorbani, Ahmad ; Soukhtanloo, Mohammad</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c270t-dc601104c87a5765b8e1bbe7d8f00d5db703c46548c151ccc6ed1f3063d72faa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Cell Line, Tumor</topic><topic>Cell Proliferation</topic><topic>Colorectal Neoplasms - drug therapy</topic><topic>Colorectal Neoplasms - genetics</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>HT29 Cells</topic><topic>Humans</topic><topic>Matrix Metalloproteinase 2 - pharmacology</topic><topic>Mice</topic><topic>Reactive Oxygen Species - metabolism</topic><topic>RNA, Messenger</topic><topic>Sesquiterpenes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Memari, Fezzeh</creatorcontrib><creatorcontrib>Mirzavi, Farshad</creatorcontrib><creatorcontrib>Jalili‐Nik, Mohammad</creatorcontrib><creatorcontrib>Afshari, Amir R.</creatorcontrib><creatorcontrib>Ghorbani, Ahmad</creatorcontrib><creatorcontrib>Soukhtanloo, Mohammad</creatorcontrib><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><jtitle>International journal of toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Memari, Fezzeh</au><au>Mirzavi, Farshad</au><au>Jalili‐Nik, Mohammad</au><au>Afshari, Amir R.</au><au>Ghorbani, Ahmad</au><au>Soukhtanloo, Mohammad</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tumor-Inhibitory Effects of Zerumbone Against HT-29 Human Colorectal Cancer Cells</atitle><jtitle>International journal of toxicology</jtitle><addtitle>Int J Toxicol</addtitle><date>2022-09</date><risdate>2022</risdate><volume>41</volume><issue>5</issue><spage>402</spage><epage>411</epage><pages>402-411</pages><issn>1091-5818</issn><eissn>1092-874X</eissn><abstract>Colorectal cancer (CRC) is the second cause of cancer-associated death globally. Recently, herbal medicinal products and, in particular, zerumbone have been widely studied and used for cancer treatment as they induce significant anti-cancer effects. However, there is limited information about the anti-cancer effects of zerumbone in CRC. Therefore, we aimed to investigate the in vitro anti-cancer effects of the zerumbone in CRC, focusing on cell apoptosis and migration. Anti-proliferative and anti-migratory effects of zerumbone on HT-29 cells were evaluated using MTT and scratch wound healing assay, respectively. Quantitative real-time PCR (qRT-PCR) was performed to determine the mRNA expression levels of migration and apoptosis-related genes. Apoptosis and cell cycle distribution were evaluated by flow cytometry. The intracellular level of reactive oxygen species (ROS) was measured using a ROS assay kit. Additionally, matrix metalloproteinase-2/-9 (MMP-2/-9) activity was determined using gelatin zymography. Zerumbone suppressed the viability of the HT-29 cells dose-dependently while having less cytotoxicity on normal NIH/3T3 cells. Zerumbone induced apoptosis in HT-29 cells and arrested the cell cycle in the G2/M phase. These effects were associated with alteration in the expression of apoptosis-related genes (up-regulation of Bax and down-regulation of Bcl-2 genes). Zerumbone also enhanced the generation of ROS in HT-29 cells. Furthermore, zerumbone significantly inhibited the migration of HT-29 cells and decreased MMP-2/-9 mRNA expression and activity. Our findings provide a potential use for zerumbone to induce apoptosis and suppress metastasis in HT-29 cells; thus, it could be developed as a promising natural agent for future CRC therapy.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>35719111</pmid><doi>10.1177/10915818221104417</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-7201-4178</orcidid></addata></record> |
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subjects | Animals Apoptosis Cell Line, Tumor Cell Proliferation Colorectal Neoplasms - drug therapy Colorectal Neoplasms - genetics Colorectal Neoplasms - metabolism HT29 Cells Humans Matrix Metalloproteinase 2 - pharmacology Mice Reactive Oxygen Species - metabolism RNA, Messenger Sesquiterpenes |
title | Tumor-Inhibitory Effects of Zerumbone Against HT-29 Human Colorectal Cancer Cells |
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