Rapid induction of apoptosis by combination of flavopiridol and tumor necrosis factor (TNF)-α or TNF-related apoptosis-inducing ligand in human cancer cell lines
Flavopiridol is one of the first cyclin-dependent kinase inhibitors undergoing clinical tests. We found that the combination treatment of flavopiridol (100-500 nM) with tumor necrosis factor (TNF)-alpha (10 ng/ml) induced a rapid and eminent apoptosis, 20 +/- 5% in 6-h treatment, in a human non-smal...
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Veröffentlicht in: | Cancer research (Chicago, Ill.) Ill.), 2003-02, Vol.63 (3), p.621-626 |
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description | Flavopiridol is one of the first cyclin-dependent kinase inhibitors undergoing clinical tests. We found that the combination treatment of flavopiridol (100-500 nM) with tumor necrosis factor (TNF)-alpha (10 ng/ml) induced a rapid and eminent apoptosis, 20 +/- 5% in 6-h treatment, in a human non-small cell lung carcinoma cell line, A549, as determined by the increase of sub-G(1) fraction in flow cytometry. A similar observation was also made in human colon cancer cell lines, HCT-116 and HCT-15, but not in Rat2, a rat fibroblast cell line. In A549 cells, the cytotoxic synergy by the combination treatment involved the activation of caspase-1, caspase-3, and caspase-8 and generated huge chromosomal degradation. The treatment schedules were so important that only the treatments of flavopiridol concomitantly with or followed by TNF-alpha showed the pronounced apoptosis in A549 cells. Prior treatment of TNF-alpha inhibited the apoptosis by the following combination treatment, leading to little cell death. Yet, such inhibition was reversed when 100 microM of 5,6-dichloro-1-beta-D-ribofuranosyl-benzimidazole, a transcription inhibitor, was present during the TNF-alpha pretreatment, suggesting that the inhibitory pretreatment of TNF-alpha might involve antiapoptotic gene expression at the transcriptional level. TNF-alpha treatment resulted in nuclear factor (NF)-kappa B activation, revealed by NF-kappa B activity reporter assay. In contrast, flavopiridol was found to inhibit the NF-kappa B-dependent gene transcription, which might give an explanation for the synergistic effect of flavopiridol with TNF-alpha. TNF-related apoptosis-inducing ligand (TRAIL; 100 ng/ml) also caused a rapid and strong cytotoxic synergy with flavopiridol. In contrast to TNF-alpha, however, all of the treatment sequences supported the synergy by TRAIL and flavopiridol. The combination of flavopiridol with TNF-alpha or TRAIL may be of use for the development in cancer therapy. |
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We found that the combination treatment of flavopiridol (100-500 nM) with tumor necrosis factor (TNF)-alpha (10 ng/ml) induced a rapid and eminent apoptosis, 20 +/- 5% in 6-h treatment, in a human non-small cell lung carcinoma cell line, A549, as determined by the increase of sub-G(1) fraction in flow cytometry. A similar observation was also made in human colon cancer cell lines, HCT-116 and HCT-15, but not in Rat2, a rat fibroblast cell line. In A549 cells, the cytotoxic synergy by the combination treatment involved the activation of caspase-1, caspase-3, and caspase-8 and generated huge chromosomal degradation. The treatment schedules were so important that only the treatments of flavopiridol concomitantly with or followed by TNF-alpha showed the pronounced apoptosis in A549 cells. Prior treatment of TNF-alpha inhibited the apoptosis by the following combination treatment, leading to little cell death. Yet, such inhibition was reversed when 100 microM of 5,6-dichloro-1-beta-D-ribofuranosyl-benzimidazole, a transcription inhibitor, was present during the TNF-alpha pretreatment, suggesting that the inhibitory pretreatment of TNF-alpha might involve antiapoptotic gene expression at the transcriptional level. TNF-alpha treatment resulted in nuclear factor (NF)-kappa B activation, revealed by NF-kappa B activity reporter assay. In contrast, flavopiridol was found to inhibit the NF-kappa B-dependent gene transcription, which might give an explanation for the synergistic effect of flavopiridol with TNF-alpha. TNF-related apoptosis-inducing ligand (TRAIL; 100 ng/ml) also caused a rapid and strong cytotoxic synergy with flavopiridol. In contrast to TNF-alpha, however, all of the treatment sequences supported the synergy by TRAIL and flavopiridol. The combination of flavopiridol with TNF-alpha or TRAIL may be of use for the development in cancer therapy.</description><identifier>ISSN: 0008-5472</identifier><identifier>EISSN: 1538-7445</identifier><identifier>PMID: 12566305</identifier><identifier>CODEN: CNREA8</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject><![CDATA[Animals ; Antineoplastic agents ; Antineoplastic Combined Chemotherapy Protocols - pharmacology ; Apoptosis - drug effects ; Apoptosis - physiology ; Apoptosis Regulatory Proteins ; Biological and medical sciences ; Carcinoma, Small Cell - drug therapy ; Carcinoma, Small Cell - enzymology ; Carcinoma, Small Cell - pathology ; Caspase Inhibitors ; Caspases - metabolism ; Chemotherapy ; Colonic Neoplasms - drug therapy ; Colonic Neoplasms - enzymology ; Colonic Neoplasms - pathology ; Drug Screening Assays, Antitumor ; Drug Synergism ; Enzyme Activation - drug effects ; Fibroblasts - drug effects ; Flavonoids - administration & dosage ; Humans ; Lung Neoplasms - drug therapy ; Lung Neoplasms - enzymology ; Lung Neoplasms - pathology ; Medical sciences ; Membrane Glycoproteins - administration & dosage ; NF-kappa B - antagonists & inhibitors ; Pharmacology. Drug treatments ; Piperidines - administration & dosage ; Rats ; Recombinant Proteins - administration & dosage ; TNF-Related Apoptosis-Inducing Ligand ; Transcriptional Activation - drug effects ; Tumor Cells, Cultured ; Tumor Necrosis Factor-alpha - administration & dosage]]></subject><ispartof>Cancer research (Chicago, Ill.), 2003-02, Vol.63 (3), p.621-626</ispartof><rights>2003 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=14505201$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12566305$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KIM, Dong-Myung</creatorcontrib><creatorcontrib>KOO, Sun-Young</creatorcontrib><creatorcontrib>JEON, Kiwan</creatorcontrib><creatorcontrib>MIN HYUNG KIM</creatorcontrib><creatorcontrib>LEE, Jinho</creatorcontrib><creatorcontrib>CHANG YONG HONG</creatorcontrib><creatorcontrib>JEONG, Shinwu</creatorcontrib><title>Rapid induction of apoptosis by combination of flavopiridol and tumor necrosis factor (TNF)-α or TNF-related apoptosis-inducing ligand in human cancer cell lines</title><title>Cancer research (Chicago, Ill.)</title><addtitle>Cancer Res</addtitle><description>Flavopiridol is one of the first cyclin-dependent kinase inhibitors undergoing clinical tests. We found that the combination treatment of flavopiridol (100-500 nM) with tumor necrosis factor (TNF)-alpha (10 ng/ml) induced a rapid and eminent apoptosis, 20 +/- 5% in 6-h treatment, in a human non-small cell lung carcinoma cell line, A549, as determined by the increase of sub-G(1) fraction in flow cytometry. A similar observation was also made in human colon cancer cell lines, HCT-116 and HCT-15, but not in Rat2, a rat fibroblast cell line. In A549 cells, the cytotoxic synergy by the combination treatment involved the activation of caspase-1, caspase-3, and caspase-8 and generated huge chromosomal degradation. The treatment schedules were so important that only the treatments of flavopiridol concomitantly with or followed by TNF-alpha showed the pronounced apoptosis in A549 cells. Prior treatment of TNF-alpha inhibited the apoptosis by the following combination treatment, leading to little cell death. Yet, such inhibition was reversed when 100 microM of 5,6-dichloro-1-beta-D-ribofuranosyl-benzimidazole, a transcription inhibitor, was present during the TNF-alpha pretreatment, suggesting that the inhibitory pretreatment of TNF-alpha might involve antiapoptotic gene expression at the transcriptional level. TNF-alpha treatment resulted in nuclear factor (NF)-kappa B activation, revealed by NF-kappa B activity reporter assay. In contrast, flavopiridol was found to inhibit the NF-kappa B-dependent gene transcription, which might give an explanation for the synergistic effect of flavopiridol with TNF-alpha. TNF-related apoptosis-inducing ligand (TRAIL; 100 ng/ml) also caused a rapid and strong cytotoxic synergy with flavopiridol. In contrast to TNF-alpha, however, all of the treatment sequences supported the synergy by TRAIL and flavopiridol. The combination of flavopiridol with TNF-alpha or TRAIL may be of use for the development in cancer therapy.</description><subject>Animals</subject><subject>Antineoplastic agents</subject><subject>Antineoplastic Combined Chemotherapy Protocols - pharmacology</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis - physiology</subject><subject>Apoptosis Regulatory Proteins</subject><subject>Biological and medical sciences</subject><subject>Carcinoma, Small Cell - drug therapy</subject><subject>Carcinoma, Small Cell - enzymology</subject><subject>Carcinoma, Small Cell - pathology</subject><subject>Caspase Inhibitors</subject><subject>Caspases - metabolism</subject><subject>Chemotherapy</subject><subject>Colonic Neoplasms - drug therapy</subject><subject>Colonic Neoplasms - enzymology</subject><subject>Colonic Neoplasms - pathology</subject><subject>Drug Screening Assays, Antitumor</subject><subject>Drug Synergism</subject><subject>Enzyme Activation - drug effects</subject><subject>Fibroblasts - drug effects</subject><subject>Flavonoids - administration & dosage</subject><subject>Humans</subject><subject>Lung Neoplasms - drug therapy</subject><subject>Lung Neoplasms - enzymology</subject><subject>Lung Neoplasms - pathology</subject><subject>Medical sciences</subject><subject>Membrane Glycoproteins - administration & dosage</subject><subject>NF-kappa B - antagonists & inhibitors</subject><subject>Pharmacology. Drug treatments</subject><subject>Piperidines - administration & dosage</subject><subject>Rats</subject><subject>Recombinant Proteins - administration & dosage</subject><subject>TNF-Related Apoptosis-Inducing Ligand</subject><subject>Transcriptional Activation - drug effects</subject><subject>Tumor Cells, Cultured</subject><subject>Tumor Necrosis Factor-alpha - administration & dosage</subject><issn>0008-5472</issn><issn>1538-7445</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFUNtKAzEUDKLYWv0FyYugD4HsJtnNPkqxKhQFqc_lbC41kk2Wza7Q3_EP_BG_yVVb-nRmmDkzh3OEpplgkpSci2M0pZRKIniZT9BZSu8jFRkVp2iS5aIoGBVT9PkCrdPYBT2o3sWAo8XQxraPySVcb7GKTe0C7DXr4SO2rnM6egxB435oYoeDUd3fhgXVj_x69bS4Id9feMQjJJ3x0Bt9iCZ_jS5ssHeb3xwX8NvQQMAKgjIdVsb7UQsmnaMTCz6Zi92codfF3Wr-QJbP94_z2yVpc1b2hBeUG2W4qPJayCoTVQE6K5QWZUlrAVIwbY2SxuZQcVmxwtQKpAWRyVozymbo8j-3HerG6HXbuQa67Xr_rNFwtTNAUuBtN17q0sHHBRU5zdgPNW53kA</recordid><startdate>20030201</startdate><enddate>20030201</enddate><creator>KIM, Dong-Myung</creator><creator>KOO, Sun-Young</creator><creator>JEON, Kiwan</creator><creator>MIN HYUNG KIM</creator><creator>LEE, Jinho</creator><creator>CHANG YONG HONG</creator><creator>JEONG, Shinwu</creator><general>American Association for Cancer Research</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>20030201</creationdate><title>Rapid induction of apoptosis by combination of flavopiridol and tumor necrosis factor (TNF)-α or TNF-related apoptosis-inducing ligand in human cancer cell lines</title><author>KIM, Dong-Myung ; KOO, Sun-Young ; JEON, Kiwan ; MIN HYUNG KIM ; LEE, Jinho ; CHANG YONG HONG ; JEONG, Shinwu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p237t-4604ece4592b5891596ad16cd5770b5a853dfec8ef2a948936ebca8fa518bd303</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Antineoplastic agents</topic><topic>Antineoplastic Combined Chemotherapy Protocols - pharmacology</topic><topic>Apoptosis - drug effects</topic><topic>Apoptosis - physiology</topic><topic>Apoptosis Regulatory Proteins</topic><topic>Biological and medical sciences</topic><topic>Carcinoma, Small Cell - drug therapy</topic><topic>Carcinoma, Small Cell - enzymology</topic><topic>Carcinoma, Small Cell - pathology</topic><topic>Caspase Inhibitors</topic><topic>Caspases - metabolism</topic><topic>Chemotherapy</topic><topic>Colonic Neoplasms - drug therapy</topic><topic>Colonic Neoplasms - enzymology</topic><topic>Colonic Neoplasms - pathology</topic><topic>Drug Screening Assays, Antitumor</topic><topic>Drug Synergism</topic><topic>Enzyme Activation - drug effects</topic><topic>Fibroblasts - drug effects</topic><topic>Flavonoids - administration & dosage</topic><topic>Humans</topic><topic>Lung Neoplasms - drug therapy</topic><topic>Lung Neoplasms - enzymology</topic><topic>Lung Neoplasms - pathology</topic><topic>Medical sciences</topic><topic>Membrane Glycoproteins - administration & dosage</topic><topic>NF-kappa B - antagonists & inhibitors</topic><topic>Pharmacology. Drug treatments</topic><topic>Piperidines - administration & dosage</topic><topic>Rats</topic><topic>Recombinant Proteins - administration & dosage</topic><topic>TNF-Related Apoptosis-Inducing Ligand</topic><topic>Transcriptional Activation - drug effects</topic><topic>Tumor Cells, Cultured</topic><topic>Tumor Necrosis Factor-alpha - administration & dosage</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>KIM, Dong-Myung</creatorcontrib><creatorcontrib>KOO, Sun-Young</creatorcontrib><creatorcontrib>JEON, Kiwan</creatorcontrib><creatorcontrib>MIN HYUNG KIM</creatorcontrib><creatorcontrib>LEE, Jinho</creatorcontrib><creatorcontrib>CHANG YONG HONG</creatorcontrib><creatorcontrib>JEONG, Shinwu</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Cancer research (Chicago, Ill.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KIM, Dong-Myung</au><au>KOO, Sun-Young</au><au>JEON, Kiwan</au><au>MIN HYUNG KIM</au><au>LEE, Jinho</au><au>CHANG YONG HONG</au><au>JEONG, Shinwu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid induction of apoptosis by combination of flavopiridol and tumor necrosis factor (TNF)-α or TNF-related apoptosis-inducing ligand in human cancer cell lines</atitle><jtitle>Cancer research (Chicago, Ill.)</jtitle><addtitle>Cancer Res</addtitle><date>2003-02-01</date><risdate>2003</risdate><volume>63</volume><issue>3</issue><spage>621</spage><epage>626</epage><pages>621-626</pages><issn>0008-5472</issn><eissn>1538-7445</eissn><coden>CNREA8</coden><abstract>Flavopiridol is one of the first cyclin-dependent kinase inhibitors undergoing clinical tests. We found that the combination treatment of flavopiridol (100-500 nM) with tumor necrosis factor (TNF)-alpha (10 ng/ml) induced a rapid and eminent apoptosis, 20 +/- 5% in 6-h treatment, in a human non-small cell lung carcinoma cell line, A549, as determined by the increase of sub-G(1) fraction in flow cytometry. A similar observation was also made in human colon cancer cell lines, HCT-116 and HCT-15, but not in Rat2, a rat fibroblast cell line. In A549 cells, the cytotoxic synergy by the combination treatment involved the activation of caspase-1, caspase-3, and caspase-8 and generated huge chromosomal degradation. The treatment schedules were so important that only the treatments of flavopiridol concomitantly with or followed by TNF-alpha showed the pronounced apoptosis in A549 cells. Prior treatment of TNF-alpha inhibited the apoptosis by the following combination treatment, leading to little cell death. Yet, such inhibition was reversed when 100 microM of 5,6-dichloro-1-beta-D-ribofuranosyl-benzimidazole, a transcription inhibitor, was present during the TNF-alpha pretreatment, suggesting that the inhibitory pretreatment of TNF-alpha might involve antiapoptotic gene expression at the transcriptional level. TNF-alpha treatment resulted in nuclear factor (NF)-kappa B activation, revealed by NF-kappa B activity reporter assay. In contrast, flavopiridol was found to inhibit the NF-kappa B-dependent gene transcription, which might give an explanation for the synergistic effect of flavopiridol with TNF-alpha. TNF-related apoptosis-inducing ligand (TRAIL; 100 ng/ml) also caused a rapid and strong cytotoxic synergy with flavopiridol. In contrast to TNF-alpha, however, all of the treatment sequences supported the synergy by TRAIL and flavopiridol. The combination of flavopiridol with TNF-alpha or TRAIL may be of use for the development in cancer therapy.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>12566305</pmid><tpages>6</tpages></addata></record> |
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source | MEDLINE; American Association for Cancer Research; EZB-FREE-00999 freely available EZB journals |
subjects | Animals Antineoplastic agents Antineoplastic Combined Chemotherapy Protocols - pharmacology Apoptosis - drug effects Apoptosis - physiology Apoptosis Regulatory Proteins Biological and medical sciences Carcinoma, Small Cell - drug therapy Carcinoma, Small Cell - enzymology Carcinoma, Small Cell - pathology Caspase Inhibitors Caspases - metabolism Chemotherapy Colonic Neoplasms - drug therapy Colonic Neoplasms - enzymology Colonic Neoplasms - pathology Drug Screening Assays, Antitumor Drug Synergism Enzyme Activation - drug effects Fibroblasts - drug effects Flavonoids - administration & dosage Humans Lung Neoplasms - drug therapy Lung Neoplasms - enzymology Lung Neoplasms - pathology Medical sciences Membrane Glycoproteins - administration & dosage NF-kappa B - antagonists & inhibitors Pharmacology. Drug treatments Piperidines - administration & dosage Rats Recombinant Proteins - administration & dosage TNF-Related Apoptosis-Inducing Ligand Transcriptional Activation - drug effects Tumor Cells, Cultured Tumor Necrosis Factor-alpha - administration & dosage |
title | Rapid induction of apoptosis by combination of flavopiridol and tumor necrosis factor (TNF)-α or TNF-related apoptosis-inducing ligand in human cancer cell lines |
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