JASMONATES INDUCE APOPTOSIS AND CELL CYCLE ARREST IN NON-SMALL CELL LUNG CANCER LINES
The jasmonates, cis-jasmone (CJ) and methyl jasmonate (MJ), were investigated for their effects against NSCLC cell lines A549 and H520. CJ or MJ inhibited the proliferation of both cell lines in a dose-dependent manner as well as induced cell cycle arrest in the G2/M phase. Apoptosis was observed fo...
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Veröffentlicht in: | Experimental lung research 2006-11, Vol.32 (10), p.499-516 |
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description | The jasmonates, cis-jasmone (CJ) and methyl jasmonate (MJ), were investigated for their effects against NSCLC cell lines A549 and H520. CJ or MJ inhibited the proliferation of both cell lines in a dose-dependent manner as well as induced cell cycle arrest in the G2/M phase. Apoptosis was observed following treatment with CJ or MJ as indicated by Hoechst staining and confirmed by dual annexin V-fluorescein isothiocyanate (FITC)/prodium iodide (PI) and DAPI (4′,6-diamidine-2′-phenylindole dihydrochloride) staining. p38 and extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation was observed with increased expression of bax, p21, and caspase-3 activity. These observations indicate that jasmonates may have a therapeutic value in the treatment of lung cancer. |
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Abiodun</creatorcontrib><creatorcontrib>Toy, Beau J.</creatorcontrib><creatorcontrib>Wang, Robert C.</creatorcontrib><title>JASMONATES INDUCE APOPTOSIS AND CELL CYCLE ARREST IN NON-SMALL CELL LUNG CANCER LINES</title><title>Experimental lung research</title><addtitle>Exp Lung Res</addtitle><description>The jasmonates, cis-jasmone (CJ) and methyl jasmonate (MJ), were investigated for their effects against NSCLC cell lines A549 and H520. CJ or MJ inhibited the proliferation of both cell lines in a dose-dependent manner as well as induced cell cycle arrest in the G2/M phase. Apoptosis was observed following treatment with CJ or MJ as indicated by Hoechst staining and confirmed by dual annexin V-fluorescein isothiocyanate (FITC)/prodium iodide (PI) and DAPI (4′,6-diamidine-2′-phenylindole dihydrochloride) staining. p38 and extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation was observed with increased expression of bax, p21, and caspase-3 activity. These observations indicate that jasmonates may have a therapeutic value in the treatment of lung cancer.</description><subject>A549</subject><subject>Acetates - pharmacology</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis Regulatory Proteins - metabolism</subject><subject>Biological and medical sciences</subject><subject>Biomarkers, Tumor - metabolism</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 Cycle - drug effects</subject><subject>Cell Line, Tumor</subject><subject>CIS-jasmone</subject><subject>Cyclopentanes - pharmacology</subject><subject>H520</subject><subject>Humans</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - metabolism</subject><subject>Lung Neoplasms - pathology</subject><subject>Medical sciences</subject><subject>methyl jasmonate</subject><subject>Neoplasm Proteins - metabolism</subject><subject>Oxylipins</subject><subject>Pneumology</subject><issn>0190-2148</issn><issn>1521-0499</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFPwjAYxRujEUT_AC9mF71Nv3Ztt0Yvy5iImRthcPC0dKWLmMGwhRj-e0fAGGPi6Tu833t530PoEsMthgDuAAsgmAIHDExwoEeoixnBLlAhjlF3p7stEHTQmbXvAEBYwE9RB_uYi4DxLpo-h_lLloaTOHeGaX8axU44ykaTLB_mTpj2nShOEid6jZJWGI_jfNJiTpqlbv4S7pSdnEzTgROFaRSPnWSYxvk5OqlkbfXF4fbQ9DGeRE9ukg2GUZi4inp07ZLKJ5RLoaQWGoNfln7bXmKfaSKYUhyUDoBirAijeFYqXjLtCSE5556vKq-Hbva5K9N8bLRdF4u5Vbqu5VI3G1vwgDBCCW9BvAeVaaw1uipWZr6QZltgKHZbFn-2bD1Xh_BNudCzH8dhvBa4PgDSKllXRi7V3P5wAfVhH_Sw5-bLqjEL-dmYelas5bZuzLfJ-6_H_S_7m5b1-k1Jo4v3ZmOW7cD_fPEF_nWXiA</recordid><startdate>20061101</startdate><enddate>20061101</enddate><creator>Yeruva, Laxmi</creator><creator>Pierre, Keon J.</creator><creator>Carper, Stephen W.</creator><creator>Elegbede, J. Abiodun</creator><creator>Toy, Beau J.</creator><creator>Wang, Robert C.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><scope>IQODW</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>7X8</scope></search><sort><creationdate>20061101</creationdate><title>JASMONATES INDUCE APOPTOSIS AND CELL CYCLE ARREST IN NON-SMALL CELL LUNG CANCER LINES</title><author>Yeruva, Laxmi ; Pierre, Keon J. ; Carper, Stephen W. ; Elegbede, J. Abiodun ; Toy, Beau J. ; Wang, Robert C.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-2f7246a9cae9e107bb7521a175e295cc60ce80411c2541dbc6b5e399a66637cf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>A549</topic><topic>Acetates - pharmacology</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Apoptosis - drug effects</topic><topic>Apoptosis Regulatory Proteins - metabolism</topic><topic>Biological and medical sciences</topic><topic>Biomarkers, Tumor - metabolism</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 Cycle - drug effects</topic><topic>Cell Line, Tumor</topic><topic>CIS-jasmone</topic><topic>Cyclopentanes - pharmacology</topic><topic>H520</topic><topic>Humans</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - metabolism</topic><topic>Lung Neoplasms - pathology</topic><topic>Medical sciences</topic><topic>methyl jasmonate</topic><topic>Neoplasm Proteins - metabolism</topic><topic>Oxylipins</topic><topic>Pneumology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yeruva, Laxmi</creatorcontrib><creatorcontrib>Pierre, Keon J.</creatorcontrib><creatorcontrib>Carper, Stephen W.</creatorcontrib><creatorcontrib>Elegbede, J. 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Apoptosis was observed following treatment with CJ or MJ as indicated by Hoechst staining and confirmed by dual annexin V-fluorescein isothiocyanate (FITC)/prodium iodide (PI) and DAPI (4′,6-diamidine-2′-phenylindole dihydrochloride) staining. p38 and extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation was observed with increased expression of bax, p21, and caspase-3 activity. These observations indicate that jasmonates may have a therapeutic value in the treatment of lung cancer.</abstract><cop>Philadelphia, PA</cop><pub>Informa UK Ltd</pub><pmid>17169856</pmid><doi>10.1080/01902140601059604</doi><tpages>18</tpages></addata></record> |
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subjects | A549 Acetates - pharmacology Antineoplastic Agents - pharmacology Apoptosis - drug effects Apoptosis Regulatory Proteins - metabolism Biological and medical sciences Biomarkers, Tumor - metabolism Carcinoma, Non-Small-Cell Lung - drug therapy Carcinoma, Non-Small-Cell Lung - metabolism Carcinoma, Non-Small-Cell Lung - pathology Cell Cycle - drug effects Cell Line, Tumor CIS-jasmone Cyclopentanes - pharmacology H520 Humans Lung Neoplasms - drug therapy Lung Neoplasms - metabolism Lung Neoplasms - pathology Medical sciences methyl jasmonate Neoplasm Proteins - metabolism Oxylipins Pneumology |
title | JASMONATES INDUCE APOPTOSIS AND CELL CYCLE ARREST IN NON-SMALL CELL LUNG CANCER LINES |
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