Anticancer activity of an essential oil from Cymbopogon flexuosus
The essential oil from a lemon grass variety of Cymbopogon flexuosus was studied for its in vitro cytotoxicity against twelve human cancer cell lines. The in vivo anticancer activity of the oil was also studied using both solid and ascitic Ehrlich and Sarcoma-180 tumor models in mice. In addition, t...
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description | The essential oil from a lemon grass variety of
Cymbopogon flexuosus was studied for its
in vitro cytotoxicity against twelve human cancer cell lines. The
in vivo anticancer activity of the oil was also studied using both solid and ascitic Ehrlich and Sarcoma-180 tumor models in mice. In addition, the morphological changes in tumor cells were studied to ascertain the mechanism of cell death. The
in vitro cytotoxicity studies showed dose-dependent effects against various human cancer cell lines. The IC
50 values of oil ranged from 4.2 to 79
μg/ml depending upon the cell line. In 502713 (colon) and IMR-32 (neuroblastoma) cell lines, the oil showed highest cytotoxicity with IC
50 value of 4.2 and 4.7
μg/ml, respectively. Intra-peritoneal administration of the oil significantly inhibited both ascitic and solid forms of Ehrlich and Sarcoma-180 tumors in a dose-dependent manner. The tumor growth inhibition at 200
mg/kg (i.p.) of the oil observed with both ascitic and solid tumor forms of Ehrlich Ascites carcinoma was 97.34 and 57.83 respectively. In case of Sarcoma-180, the growth inhibition at similar dose of oil was 94.07 and 36.97% in ascitic and solid forms respectively. Morphological studies of the oil treated HL-60 cells revealed loss of surface projections, chromatin condensation and apoptosis. The mitochondria showed apparent loss of cristae in the cells undergoing apoptosis. The morphological studies of Sarcoma-180 solid tumor cells from animals treated with the oil revealed condensation and fragmentation of nuclei typical of apoptosis. Morphological studies of ascites cells from animals treated with the oil too revealed the changes typical of apoptosis. Our results indicate that the oil has a promising anticancer activity and causes loss in tumor cell viability by activating the apoptotic process as identified by electron microscopy. |
doi_str_mv | 10.1016/j.cbi.2008.12.004 |
format | Article |
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Cymbopogon flexuosus was studied for its
in vitro cytotoxicity against twelve human cancer cell lines. The
in vivo anticancer activity of the oil was also studied using both solid and ascitic Ehrlich and Sarcoma-180 tumor models in mice. In addition, the morphological changes in tumor cells were studied to ascertain the mechanism of cell death. The
in vitro cytotoxicity studies showed dose-dependent effects against various human cancer cell lines. The IC
50 values of oil ranged from 4.2 to 79
μg/ml depending upon the cell line. In 502713 (colon) and IMR-32 (neuroblastoma) cell lines, the oil showed highest cytotoxicity with IC
50 value of 4.2 and 4.7
μg/ml, respectively. Intra-peritoneal administration of the oil significantly inhibited both ascitic and solid forms of Ehrlich and Sarcoma-180 tumors in a dose-dependent manner. The tumor growth inhibition at 200
mg/kg (i.p.) of the oil observed with both ascitic and solid tumor forms of Ehrlich Ascites carcinoma was 97.34 and 57.83 respectively. In case of Sarcoma-180, the growth inhibition at similar dose of oil was 94.07 and 36.97% in ascitic and solid forms respectively. Morphological studies of the oil treated HL-60 cells revealed loss of surface projections, chromatin condensation and apoptosis. The mitochondria showed apparent loss of cristae in the cells undergoing apoptosis. The morphological studies of Sarcoma-180 solid tumor cells from animals treated with the oil revealed condensation and fragmentation of nuclei typical of apoptosis. Morphological studies of ascites cells from animals treated with the oil too revealed the changes typical of apoptosis. Our results indicate that the oil has a promising anticancer activity and causes loss in tumor cell viability by activating the apoptotic process as identified by electron microscopy.</description><identifier>ISSN: 0009-2797</identifier><identifier>EISSN: 1872-7786</identifier><identifier>DOI: 10.1016/j.cbi.2008.12.004</identifier><identifier>PMID: 19121295</identifier><language>eng</language><publisher>Ireland: Elsevier Ireland Ltd</publisher><subject>Animal models ; Animals ; Antineoplastic Agents, Phytogenic - pharmacology ; Apoptosis ; Apoptosis - drug effects ; Cell Proliferation - drug effects ; Cell Survival - drug effects ; Cymbopogon - chemistry ; Cymbopogon flexuosus ; Cytotoxicity ; Disease Models, Animal ; Dose-Response Relationship, Drug ; Drug Screening Assays, Antitumor ; Essential oil ; HL-60 Cells ; Humans ; Mice ; Mice, Inbred BALB C ; Neoplasms, Experimental - drug therapy ; Neoplasms, Experimental - pathology ; Oils, Volatile - pharmacology ; Tumor Cells, Cultured ; Tumor growth inhibition</subject><ispartof>Chemico-biological interactions, 2009-05, Vol.179 (2), p.160-168</ispartof><rights>2008 Elsevier Ireland Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-db86c95a832ade46662d06b75055a2bb2739e27be77cd0c35251d9c2ea4314a53</citedby><cites>FETCH-LOGICAL-c448t-db86c95a832ade46662d06b75055a2bb2739e27be77cd0c35251d9c2ea4314a53</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0009279708006613$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19121295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sharma, Parduman R.</creatorcontrib><creatorcontrib>Mondhe, Dilip M.</creatorcontrib><creatorcontrib>Muthiah, Shanmugavel</creatorcontrib><creatorcontrib>Pal, Harish C.</creatorcontrib><creatorcontrib>Shahi, Ashok K.</creatorcontrib><creatorcontrib>Saxena, Ajit K.</creatorcontrib><creatorcontrib>Qazi, Ghulam N.</creatorcontrib><title>Anticancer activity of an essential oil from Cymbopogon flexuosus</title><title>Chemico-biological interactions</title><addtitle>Chem Biol Interact</addtitle><description>The essential oil from a lemon grass variety of
Cymbopogon flexuosus was studied for its
in vitro cytotoxicity against twelve human cancer cell lines. The
in vivo anticancer activity of the oil was also studied using both solid and ascitic Ehrlich and Sarcoma-180 tumor models in mice. In addition, the morphological changes in tumor cells were studied to ascertain the mechanism of cell death. The
in vitro cytotoxicity studies showed dose-dependent effects against various human cancer cell lines. The IC
50 values of oil ranged from 4.2 to 79
μg/ml depending upon the cell line. In 502713 (colon) and IMR-32 (neuroblastoma) cell lines, the oil showed highest cytotoxicity with IC
50 value of 4.2 and 4.7
μg/ml, respectively. Intra-peritoneal administration of the oil significantly inhibited both ascitic and solid forms of Ehrlich and Sarcoma-180 tumors in a dose-dependent manner. The tumor growth inhibition at 200
mg/kg (i.p.) of the oil observed with both ascitic and solid tumor forms of Ehrlich Ascites carcinoma was 97.34 and 57.83 respectively. In case of Sarcoma-180, the growth inhibition at similar dose of oil was 94.07 and 36.97% in ascitic and solid forms respectively. Morphological studies of the oil treated HL-60 cells revealed loss of surface projections, chromatin condensation and apoptosis. The mitochondria showed apparent loss of cristae in the cells undergoing apoptosis. The morphological studies of Sarcoma-180 solid tumor cells from animals treated with the oil revealed condensation and fragmentation of nuclei typical of apoptosis. Morphological studies of ascites cells from animals treated with the oil too revealed the changes typical of apoptosis. Our results indicate that the oil has a promising anticancer activity and causes loss in tumor cell viability by activating the apoptotic process as identified by electron microscopy.</description><subject>Animal models</subject><subject>Animals</subject><subject>Antineoplastic Agents, Phytogenic - pharmacology</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Cell Proliferation - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Cymbopogon - chemistry</subject><subject>Cymbopogon flexuosus</subject><subject>Cytotoxicity</subject><subject>Disease Models, Animal</subject><subject>Dose-Response Relationship, Drug</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Essential oil</subject><subject>HL-60 Cells</subject><subject>Humans</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Neoplasms, Experimental - drug therapy</subject><subject>Neoplasms, Experimental - pathology</subject><subject>Oils, Volatile - pharmacology</subject><subject>Tumor Cells, Cultured</subject><subject>Tumor growth inhibition</subject><issn>0009-2797</issn><issn>1872-7786</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkD1PwzAURS0EoqXwA1hQJrYE24ljW0xVxZdUiQVmy3ZekKskLnaC6L_HVSuxwfR09c69w0HomuCCYFLfbQprXEExFgWhBcbVCZoTwWnOuahP0RxjLHPKJZ-hixg3KWJa4XM0I5JQQiWbo-VyGJ3Vg4WQaTu6LzfuMt9mesggRkhP3WXedVkbfJ-tdr3xW__hh6zt4HvycYqX6KzVXYSr412g98eHt9Vzvn59elkt17mtKjHmjRG1lUyLkuoGqrquaYNrwxlmTFNjKC8lUG6Ac9tgWzLKSCMtBV2VpNKsXKDbw-42-M8J4qh6Fy10nR7AT1HVHDMpifgXTL6kLEuZQHIAbfAxBmjVNrheh50iWO0Fq41KgvcFoQhVSXDq3BzHJ9ND89s4Gk3A_QGA5OLLQVDROkh-GxfAjqrx7o_5H6KVirM</recordid><startdate>20090515</startdate><enddate>20090515</enddate><creator>Sharma, Parduman R.</creator><creator>Mondhe, Dilip M.</creator><creator>Muthiah, Shanmugavel</creator><creator>Pal, Harish C.</creator><creator>Shahi, Ashok K.</creator><creator>Saxena, Ajit K.</creator><creator>Qazi, Ghulam N.</creator><general>Elsevier Ireland Ltd</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>7QO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>20090515</creationdate><title>Anticancer activity of an essential oil from Cymbopogon flexuosus</title><author>Sharma, Parduman R. ; Mondhe, Dilip M. ; Muthiah, Shanmugavel ; Pal, Harish C. ; Shahi, Ashok K. ; Saxena, Ajit K. ; Qazi, Ghulam N.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-db86c95a832ade46662d06b75055a2bb2739e27be77cd0c35251d9c2ea4314a53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Antineoplastic Agents, Phytogenic - pharmacology</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Cell Proliferation - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Cymbopogon - chemistry</topic><topic>Cymbopogon flexuosus</topic><topic>Cytotoxicity</topic><topic>Disease Models, Animal</topic><topic>Dose-Response Relationship, Drug</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Essential oil</topic><topic>HL-60 Cells</topic><topic>Humans</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Neoplasms, Experimental - drug therapy</topic><topic>Neoplasms, Experimental - pathology</topic><topic>Oils, Volatile - pharmacology</topic><topic>Tumor Cells, Cultured</topic><topic>Tumor growth inhibition</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sharma, Parduman R.</creatorcontrib><creatorcontrib>Mondhe, Dilip M.</creatorcontrib><creatorcontrib>Muthiah, Shanmugavel</creatorcontrib><creatorcontrib>Pal, Harish C.</creatorcontrib><creatorcontrib>Shahi, Ashok K.</creatorcontrib><creatorcontrib>Saxena, Ajit K.</creatorcontrib><creatorcontrib>Qazi, Ghulam N.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Chemico-biological interactions</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sharma, Parduman R.</au><au>Mondhe, Dilip M.</au><au>Muthiah, Shanmugavel</au><au>Pal, Harish C.</au><au>Shahi, Ashok K.</au><au>Saxena, Ajit K.</au><au>Qazi, Ghulam N.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Anticancer activity of an essential oil from Cymbopogon flexuosus</atitle><jtitle>Chemico-biological interactions</jtitle><addtitle>Chem Biol Interact</addtitle><date>2009-05-15</date><risdate>2009</risdate><volume>179</volume><issue>2</issue><spage>160</spage><epage>168</epage><pages>160-168</pages><issn>0009-2797</issn><eissn>1872-7786</eissn><abstract>The essential oil from a lemon grass variety of
Cymbopogon flexuosus was studied for its
in vitro cytotoxicity against twelve human cancer cell lines. The
in vivo anticancer activity of the oil was also studied using both solid and ascitic Ehrlich and Sarcoma-180 tumor models in mice. In addition, the morphological changes in tumor cells were studied to ascertain the mechanism of cell death. The
in vitro cytotoxicity studies showed dose-dependent effects against various human cancer cell lines. The IC
50 values of oil ranged from 4.2 to 79
μg/ml depending upon the cell line. In 502713 (colon) and IMR-32 (neuroblastoma) cell lines, the oil showed highest cytotoxicity with IC
50 value of 4.2 and 4.7
μg/ml, respectively. Intra-peritoneal administration of the oil significantly inhibited both ascitic and solid forms of Ehrlich and Sarcoma-180 tumors in a dose-dependent manner. The tumor growth inhibition at 200
mg/kg (i.p.) of the oil observed with both ascitic and solid tumor forms of Ehrlich Ascites carcinoma was 97.34 and 57.83 respectively. In case of Sarcoma-180, the growth inhibition at similar dose of oil was 94.07 and 36.97% in ascitic and solid forms respectively. Morphological studies of the oil treated HL-60 cells revealed loss of surface projections, chromatin condensation and apoptosis. The mitochondria showed apparent loss of cristae in the cells undergoing apoptosis. The morphological studies of Sarcoma-180 solid tumor cells from animals treated with the oil revealed condensation and fragmentation of nuclei typical of apoptosis. Morphological studies of ascites cells from animals treated with the oil too revealed the changes typical of apoptosis. Our results indicate that the oil has a promising anticancer activity and causes loss in tumor cell viability by activating the apoptotic process as identified by electron microscopy.</abstract><cop>Ireland</cop><pub>Elsevier Ireland Ltd</pub><pmid>19121295</pmid><doi>10.1016/j.cbi.2008.12.004</doi><tpages>9</tpages></addata></record> |
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subjects | Animal models Animals Antineoplastic Agents, Phytogenic - pharmacology Apoptosis Apoptosis - drug effects Cell Proliferation - drug effects Cell Survival - drug effects Cymbopogon - chemistry Cymbopogon flexuosus Cytotoxicity Disease Models, Animal Dose-Response Relationship, Drug Drug Screening Assays, Antitumor Essential oil HL-60 Cells Humans Mice Mice, Inbred BALB C Neoplasms, Experimental - drug therapy Neoplasms, Experimental - pathology Oils, Volatile - pharmacology Tumor Cells, Cultured Tumor growth inhibition |
title | Anticancer activity of an essential oil from Cymbopogon flexuosus |
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