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Essential Oil Extracted from Rhizoma of Atractylode Lancea Induces Oncosis in Human MKN-45 Cancer Cells
The aim of this study was to examine whether the essential oil extracted from rhizoma of Atractylode lancea has cytotoxicity to human MKN-45 cancer cells and its underlying mechanisms. The cytotoxicity of essential oil to cancer cells was examined by MTT assay. The effects of essential oil and disru...
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Published in: | European journal of inflammation 2013-05, Vol.11 (2), p.397-403 |
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container_title | European journal of inflammation |
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creator | Chen, H-N. Shao, C. Zhao, J-Z. Guan, X-W. Ding, J. Shao, S-H. |
description | The aim of this study was to examine whether the essential oil extracted from rhizoma of Atractylode lancea has cytotoxicity to human MKN-45 cancer cells and its underlying mechanisms. The cytotoxicity of essential oil to cancer cells was examined by MTT assay. The effects of essential oil and disruption were monitored using whole-cell, time-lapse recording by microscopy. The effects of essential oil on cytoskeletal systems were detected by Western blotting and immunofluorescence. The effects of essential oil on cytokine secretion were measured by ELISA. The result showed that the cytotoxicity of essential oil was triggered rapidly by 2 μl/ml (1 h caused 50% maximum cytotoxicity) and involved secretion function perturbation. In addition, essential oil could induce membrane blebbing within 1 h of sustained application, which was blocked by polyethylene glycols (PEG) with molecular weights £3350, but not prevented by PEG with molecular weight34000 and extracellular calcium chelator EGTA. Moreover, essential oil did not disrupt cytoskeletal systems as demonstrated with no degradation of microtubules and actin. In conclusion, essential oil extracted from rhizoma of Atractylode lancea can rapidly initiate acute injury and burst via oncosis and may offer a novel therapeutic strategy for cancer treatment. |
doi_str_mv | 10.1177/1721727X1301100210 |
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The cytotoxicity of essential oil to cancer cells was examined by MTT assay. The effects of essential oil and disruption were monitored using whole-cell, time-lapse recording by microscopy. The effects of essential oil on cytoskeletal systems were detected by Western blotting and immunofluorescence. The effects of essential oil on cytokine secretion were measured by ELISA. The result showed that the cytotoxicity of essential oil was triggered rapidly by 2 μl/ml (1 h caused 50% maximum cytotoxicity) and involved secretion function perturbation. In addition, essential oil could induce membrane blebbing within 1 h of sustained application, which was blocked by polyethylene glycols (PEG) with molecular weights £3350, but not prevented by PEG with molecular weight34000 and extracellular calcium chelator EGTA. Moreover, essential oil did not disrupt cytoskeletal systems as demonstrated with no degradation of microtubules and actin. 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The cytotoxicity of essential oil to cancer cells was examined by MTT assay. The effects of essential oil and disruption were monitored using whole-cell, time-lapse recording by microscopy. The effects of essential oil on cytoskeletal systems were detected by Western blotting and immunofluorescence. The effects of essential oil on cytokine secretion were measured by ELISA. The result showed that the cytotoxicity of essential oil was triggered rapidly by 2 μl/ml (1 h caused 50% maximum cytotoxicity) and involved secretion function perturbation. In addition, essential oil could induce membrane blebbing within 1 h of sustained application, which was blocked by polyethylene glycols (PEG) with molecular weights £3350, but not prevented by PEG with molecular weight34000 and extracellular calcium chelator EGTA. Moreover, essential oil did not disrupt cytoskeletal systems as demonstrated with no degradation of microtubules and actin. In conclusion, essential oil extracted from rhizoma of Atractylode lancea can rapidly initiate acute injury and burst via oncosis and may offer a novel therapeutic strategy for cancer treatment.</description><subject>Cancer</subject><subject>Cytotoxicity</subject><subject>Oils & fats</subject><issn>2058-7392</issn><issn>1721-727X</issn><issn>2058-7392</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9UF1Lw0AQPETBUvsHfDrwOfY-csnlsYRqi9WCKPgW7i57NSXJ1bsErL_e1AoKgsuys7AzszAIXVJyTWmaTmnKhk5fKCeUEsIoOUEjRoSMUp6x01_7OZqEsCVDJSxJMzlCm3kI0HaVqvG6qvH8vfPKdFBi612DH1-rD9co7CyefR32tSsBr1RrQOFlW_YGAl63xoUq4KrFi75RLb6_e4higfMDzeMc6jpcoDOr6gCTbxyj55v5U76IVuvbZT5bRYaLrIu4tCBZmYCNBYAuiUlirbU0XCVZQllCSpXR1GZWM0MFMyBEKSTTAFJrkHyMro6-O-_eeghdsXW9b4eXBeMx42KYYmCxI8t4F4IHW-x81Si_LygpDpkWfzMdRNOjKKgN_Nj-o_gEJcR2MQ</recordid><startdate>20130501</startdate><enddate>20130501</enddate><creator>Chen, H-N.</creator><creator>Shao, C.</creator><creator>Zhao, J-Z.</creator><creator>Guan, X-W.</creator><creator>Ding, J.</creator><creator>Shao, S-H.</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20130501</creationdate><title>Essential Oil Extracted from Rhizoma of Atractylode Lancea Induces Oncosis in Human MKN-45 Cancer Cells</title><author>Chen, H-N. ; Shao, C. ; Zhao, J-Z. ; Guan, X-W. ; Ding, J. ; Shao, S-H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c359t-38fe82d6ef45eebd0c64bbb8c3a6961260da917f9fb2c152ce55d582bee8bbe83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Cancer</topic><topic>Cytotoxicity</topic><topic>Oils & fats</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, H-N.</creatorcontrib><creatorcontrib>Shao, C.</creatorcontrib><creatorcontrib>Zhao, J-Z.</creatorcontrib><creatorcontrib>Guan, X-W.</creatorcontrib><creatorcontrib>Ding, J.</creatorcontrib><creatorcontrib>Shao, S-H.</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>European journal of inflammation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Chen, H-N.</au><au>Shao, C.</au><au>Zhao, J-Z.</au><au>Guan, X-W.</au><au>Ding, J.</au><au>Shao, S-H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Essential Oil Extracted from Rhizoma of Atractylode Lancea Induces Oncosis in Human MKN-45 Cancer Cells</atitle><jtitle>European journal of inflammation</jtitle><date>2013-05-01</date><risdate>2013</risdate><volume>11</volume><issue>2</issue><spage>397</spage><epage>403</epage><pages>397-403</pages><issn>2058-7392</issn><issn>1721-727X</issn><eissn>2058-7392</eissn><abstract>The aim of this study was to examine whether the essential oil extracted from rhizoma of Atractylode lancea has cytotoxicity to human MKN-45 cancer cells and its underlying mechanisms. The cytotoxicity of essential oil to cancer cells was examined by MTT assay. The effects of essential oil and disruption were monitored using whole-cell, time-lapse recording by microscopy. The effects of essential oil on cytoskeletal systems were detected by Western blotting and immunofluorescence. The effects of essential oil on cytokine secretion were measured by ELISA. The result showed that the cytotoxicity of essential oil was triggered rapidly by 2 μl/ml (1 h caused 50% maximum cytotoxicity) and involved secretion function perturbation. In addition, essential oil could induce membrane blebbing within 1 h of sustained application, which was blocked by polyethylene glycols (PEG) with molecular weights £3350, but not prevented by PEG with molecular weight34000 and extracellular calcium chelator EGTA. Moreover, essential oil did not disrupt cytoskeletal systems as demonstrated with no degradation of microtubules and actin. 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title | Essential Oil Extracted from Rhizoma of Atractylode Lancea Induces Oncosis in Human MKN-45 Cancer Cells |
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