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Terpenoids Isolated From the Shoot of Plectranthus hadiensis Induces Apoptosis in Human Colon Cancer Cells Via the Mitochondria-Dependent Pathway
The plant Plectranthus hadiensis is a rich source of many bioactive phytochemicals, especially terpenoids. The terpenoid fraction was isolated and phytochemical characterization was done using GC-MS. The aim of the present study was to find out the antiproliferative activity and the mechanism of cel...
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Published in: | Nutrition and cancer 2015-05, Vol.67 (4), p.697-705 |
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description | The plant Plectranthus hadiensis is a rich source of many bioactive phytochemicals, especially terpenoids. The terpenoid fraction was isolated and phytochemical characterization was done using GC-MS. The aim of the present study was to find out the antiproliferative activity and the mechanism of cell death induction by the terpenoid fraction on human colon cancer cells (HCT-15). MTT assay was performed with different concentrations of the fraction (10, 20, and 50 µg/mL) to obtain IC50 value for 24 h to induce cell death. The induction of apoptosis were studied by Hoechst staining, acridine orange/ethidium bromide staining, Comet assay, DNA fragmentation, and caspase-3 activity assays. The mechanism of apoptosis induction was studied by expression analysis of antiapoptotic Bcl-2 and proapoptotic Bax using RT-PCR and also by Western blot analysis of proteins involved in the apoptotic pathway. The terpenoid fraction induced significant morphological changes and DNA fragmentation in the cells. Positive Hoechst staining and acridine orange/ethidium bromide staining indicated apoptosis induction by the fraction. DNA fragmentation, which is a characteristic feature of apoptosis, was also observed. Upregulation of caspase-3 activity and proapoptotic Bax, and the downregulation of antiapoptotic Bcl-2 and COX-2 confirmed that the apoptosis induction was via the mitochondria-dependent pathway. |
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K</creator><creatorcontrib>Menon, Darsan B ; Gopalakrishnan, V. K</creatorcontrib><description>The plant Plectranthus hadiensis is a rich source of many bioactive phytochemicals, especially terpenoids. The terpenoid fraction was isolated and phytochemical characterization was done using GC-MS. The aim of the present study was to find out the antiproliferative activity and the mechanism of cell death induction by the terpenoid fraction on human colon cancer cells (HCT-15). MTT assay was performed with different concentrations of the fraction (10, 20, and 50 µg/mL) to obtain IC50 value for 24 h to induce cell death. The induction of apoptosis were studied by Hoechst staining, acridine orange/ethidium bromide staining, Comet assay, DNA fragmentation, and caspase-3 activity assays. The mechanism of apoptosis induction was studied by expression analysis of antiapoptotic Bcl-2 and proapoptotic Bax using RT-PCR and also by Western blot analysis of proteins involved in the apoptotic pathway. The terpenoid fraction induced significant morphological changes and DNA fragmentation in the cells. Positive Hoechst staining and acridine orange/ethidium bromide staining indicated apoptosis induction by the fraction. DNA fragmentation, which is a characteristic feature of apoptosis, was also observed. Upregulation of caspase-3 activity and proapoptotic Bax, and the downregulation of antiapoptotic Bcl-2 and COX-2 confirmed that the apoptosis induction was via the mitochondria-dependent pathway.</description><identifier>ISSN: 1532-7914</identifier><identifier>ISSN: 0163-5581</identifier><identifier>EISSN: 1532-7914</identifier><identifier>DOI: 10.1080/01635581.2015.1019631</identifier><identifier>PMID: 25837437</identifier><language>eng</language><publisher>United States: Routledge</publisher><subject>acridine orange ; Apoptosis ; Apoptosis - drug effects ; Caspase 3 - genetics ; Caspase 3 - metabolism ; caspase-3 ; Cell Line, Tumor - drug effects ; Cell Survival - drug effects ; Cells ; Colonic Neoplasms - metabolism ; Colonic Neoplasms - pathology ; Colorectal cancer ; colorectal neoplasms ; Comet Assay ; Cyclooxygenase 2 - genetics ; Cyclooxygenase 2 - metabolism ; Deoxyribonucleic acid ; DNA ; DNA Fragmentation ; ethidium ; Gas Chromatography-Mass Spectrometry ; Humans ; inhibitory concentration 50 ; Mitochondria - drug effects ; Mitochondria - metabolism ; neoplasm cells ; Phytochemicals ; phytopharmaceuticals ; Plant Extracts - pharmacology ; Plectranthus ; Plectranthus - chemistry ; Proteins ; Proto-Oncogene Proteins c-bcl-2 - genetics ; Proto-Oncogene Proteins c-bcl-2 - metabolism ; reverse transcriptase polymerase chain reaction ; Terpenes - pharmacology ; terpenoids ; Up-Regulation ; Western blotting</subject><ispartof>Nutrition and cancer, 2015-05, Vol.67 (4), p.697-705</ispartof><rights>Copyright © 2015, Taylor & Francis Group, LLC 2015</rights><rights>Copyright Taylor & Francis Ltd. 2015</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c418t-98d6f7e3e0c4703856c57c314e2803a8467dbac2c5bd0a69e9e08a91aa4188663</citedby><cites>FETCH-LOGICAL-c418t-98d6f7e3e0c4703856c57c314e2803a8467dbac2c5bd0a69e9e08a91aa4188663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,778,782,27911,27912</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25837437$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Menon, Darsan B</creatorcontrib><creatorcontrib>Gopalakrishnan, V. K</creatorcontrib><title>Terpenoids Isolated From the Shoot of Plectranthus hadiensis Induces Apoptosis in Human Colon Cancer Cells Via the Mitochondria-Dependent Pathway</title><title>Nutrition and cancer</title><addtitle>Nutr Cancer</addtitle><description>The plant Plectranthus hadiensis is a rich source of many bioactive phytochemicals, especially terpenoids. The terpenoid fraction was isolated and phytochemical characterization was done using GC-MS. The aim of the present study was to find out the antiproliferative activity and the mechanism of cell death induction by the terpenoid fraction on human colon cancer cells (HCT-15). MTT assay was performed with different concentrations of the fraction (10, 20, and 50 µg/mL) to obtain IC50 value for 24 h to induce cell death. The induction of apoptosis were studied by Hoechst staining, acridine orange/ethidium bromide staining, Comet assay, DNA fragmentation, and caspase-3 activity assays. The mechanism of apoptosis induction was studied by expression analysis of antiapoptotic Bcl-2 and proapoptotic Bax using RT-PCR and also by Western blot analysis of proteins involved in the apoptotic pathway. The terpenoid fraction induced significant morphological changes and DNA fragmentation in the cells. Positive Hoechst staining and acridine orange/ethidium bromide staining indicated apoptosis induction by the fraction. DNA fragmentation, which is a characteristic feature of apoptosis, was also observed. Upregulation of caspase-3 activity and proapoptotic Bax, and the downregulation of antiapoptotic Bcl-2 and COX-2 confirmed that the apoptosis induction was via the mitochondria-dependent pathway.</description><subject>acridine orange</subject><subject>Apoptosis</subject><subject>Apoptosis - drug effects</subject><subject>Caspase 3 - genetics</subject><subject>Caspase 3 - metabolism</subject><subject>caspase-3</subject><subject>Cell Line, Tumor - drug effects</subject><subject>Cell Survival - drug effects</subject><subject>Cells</subject><subject>Colonic Neoplasms - metabolism</subject><subject>Colonic Neoplasms - pathology</subject><subject>Colorectal cancer</subject><subject>colorectal neoplasms</subject><subject>Comet Assay</subject><subject>Cyclooxygenase 2 - genetics</subject><subject>Cyclooxygenase 2 - metabolism</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA Fragmentation</subject><subject>ethidium</subject><subject>Gas Chromatography-Mass Spectrometry</subject><subject>Humans</subject><subject>inhibitory concentration 50</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>neoplasm cells</subject><subject>Phytochemicals</subject><subject>phytopharmaceuticals</subject><subject>Plant Extracts - pharmacology</subject><subject>Plectranthus</subject><subject>Plectranthus - chemistry</subject><subject>Proteins</subject><subject>Proto-Oncogene Proteins c-bcl-2 - genetics</subject><subject>Proto-Oncogene Proteins c-bcl-2 - metabolism</subject><subject>reverse transcriptase polymerase chain reaction</subject><subject>Terpenes - pharmacology</subject><subject>terpenoids</subject><subject>Up-Regulation</subject><subject>Western blotting</subject><issn>1532-7914</issn><issn>0163-5581</issn><issn>1532-7914</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFks9u1DAQxiMEon_gEQBLXHrZYseJ7dyoFkorFVGpLVdr1p4QV4m9tR1V-xi8MV52ixAXLrY1-n3fjOZzVb1h9JRRRT9QJnjbKnZaU9aWEusEZ8-qQ9byeiE71jz_631QHaV0TymVjKuX1UHdKi4bLg-rn7cY1-iDs4lcpjBCRkvOY5hIHpDcDCFkEnpyPaLJEXwe5kQGsA59ckXh7WwwkbN1WOewrThPLuYJPFmGMZQTvMFIljiOiXx38Nv1q8vBDMHb6GDxCUt7iz6Ta8jDI2xeVS96GBO-3t_H1d3559vlxeLq25fL5dnVwjRM5UWnrOglcqSmkZSrVphWGs4arBXloBoh7QpMbdqVpSA67JAq6BhAkSsh-HF1svNdx_AwY8p6csmUQcFjmJNmQkrVlb3Sgr7_B70Pc_RlukKpWnSKqaZQ7Y4yMaQUsdfr6CaIG82o3mamnzLT28z0PrOie7t3n1cT2j-qp5AK8HEHON-HOMFjiKPVGTZjiH0Jxbik-f96vNtZ9BA0_IhFcXdTCFH-hJKNoPwX4c2vdg</recordid><startdate>20150519</startdate><enddate>20150519</enddate><creator>Menon, Darsan B</creator><creator>Gopalakrishnan, V. K</creator><general>Routledge</general><general>Taylor & Francis Ltd</general><scope>FBQ</scope><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>7U7</scope><scope>C1K</scope><scope>7X8</scope></search><sort><creationdate>20150519</creationdate><title>Terpenoids Isolated From the Shoot of Plectranthus hadiensis Induces Apoptosis in Human Colon Cancer Cells Via the Mitochondria-Dependent Pathway</title><author>Menon, Darsan B ; Gopalakrishnan, V. K</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c418t-98d6f7e3e0c4703856c57c314e2803a8467dbac2c5bd0a69e9e08a91aa4188663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>acridine orange</topic><topic>Apoptosis</topic><topic>Apoptosis - drug effects</topic><topic>Caspase 3 - genetics</topic><topic>Caspase 3 - metabolism</topic><topic>caspase-3</topic><topic>Cell Line, Tumor - drug effects</topic><topic>Cell Survival - drug effects</topic><topic>Cells</topic><topic>Colonic Neoplasms - metabolism</topic><topic>Colonic Neoplasms - pathology</topic><topic>Colorectal cancer</topic><topic>colorectal neoplasms</topic><topic>Comet Assay</topic><topic>Cyclooxygenase 2 - genetics</topic><topic>Cyclooxygenase 2 - metabolism</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA Fragmentation</topic><topic>ethidium</topic><topic>Gas Chromatography-Mass Spectrometry</topic><topic>Humans</topic><topic>inhibitory concentration 50</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>neoplasm cells</topic><topic>Phytochemicals</topic><topic>phytopharmaceuticals</topic><topic>Plant Extracts - pharmacology</topic><topic>Plectranthus</topic><topic>Plectranthus - chemistry</topic><topic>Proteins</topic><topic>Proto-Oncogene Proteins c-bcl-2 - genetics</topic><topic>Proto-Oncogene Proteins c-bcl-2 - metabolism</topic><topic>reverse transcriptase polymerase chain reaction</topic><topic>Terpenes - pharmacology</topic><topic>terpenoids</topic><topic>Up-Regulation</topic><topic>Western blotting</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Menon, Darsan B</creatorcontrib><creatorcontrib>Gopalakrishnan, V. K</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Nutrition and cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Menon, Darsan B</au><au>Gopalakrishnan, V. K</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Terpenoids Isolated From the Shoot of Plectranthus hadiensis Induces Apoptosis in Human Colon Cancer Cells Via the Mitochondria-Dependent Pathway</atitle><jtitle>Nutrition and cancer</jtitle><addtitle>Nutr Cancer</addtitle><date>2015-05-19</date><risdate>2015</risdate><volume>67</volume><issue>4</issue><spage>697</spage><epage>705</epage><pages>697-705</pages><issn>1532-7914</issn><issn>0163-5581</issn><eissn>1532-7914</eissn><abstract>The plant Plectranthus hadiensis is a rich source of many bioactive phytochemicals, especially terpenoids. The terpenoid fraction was isolated and phytochemical characterization was done using GC-MS. The aim of the present study was to find out the antiproliferative activity and the mechanism of cell death induction by the terpenoid fraction on human colon cancer cells (HCT-15). MTT assay was performed with different concentrations of the fraction (10, 20, and 50 µg/mL) to obtain IC50 value for 24 h to induce cell death. The induction of apoptosis were studied by Hoechst staining, acridine orange/ethidium bromide staining, Comet assay, DNA fragmentation, and caspase-3 activity assays. The mechanism of apoptosis induction was studied by expression analysis of antiapoptotic Bcl-2 and proapoptotic Bax using RT-PCR and also by Western blot analysis of proteins involved in the apoptotic pathway. The terpenoid fraction induced significant morphological changes and DNA fragmentation in the cells. Positive Hoechst staining and acridine orange/ethidium bromide staining indicated apoptosis induction by the fraction. DNA fragmentation, which is a characteristic feature of apoptosis, was also observed. Upregulation of caspase-3 activity and proapoptotic Bax, and the downregulation of antiapoptotic Bcl-2 and COX-2 confirmed that the apoptosis induction was via the mitochondria-dependent pathway.</abstract><cop>United States</cop><pub>Routledge</pub><pmid>25837437</pmid><doi>10.1080/01635581.2015.1019631</doi><tpages>9</tpages></addata></record> |
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subjects | acridine orange Apoptosis Apoptosis - drug effects Caspase 3 - genetics Caspase 3 - metabolism caspase-3 Cell Line, Tumor - drug effects Cell Survival - drug effects Cells Colonic Neoplasms - metabolism Colonic Neoplasms - pathology Colorectal cancer colorectal neoplasms Comet Assay Cyclooxygenase 2 - genetics Cyclooxygenase 2 - metabolism Deoxyribonucleic acid DNA DNA Fragmentation ethidium Gas Chromatography-Mass Spectrometry Humans inhibitory concentration 50 Mitochondria - drug effects Mitochondria - metabolism neoplasm cells Phytochemicals phytopharmaceuticals Plant Extracts - pharmacology Plectranthus Plectranthus - chemistry Proteins Proto-Oncogene Proteins c-bcl-2 - genetics Proto-Oncogene Proteins c-bcl-2 - metabolism reverse transcriptase polymerase chain reaction Terpenes - pharmacology terpenoids Up-Regulation Western blotting |
title | Terpenoids Isolated From the Shoot of Plectranthus hadiensis Induces Apoptosis in Human Colon Cancer Cells Via the Mitochondria-Dependent Pathway |
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