Piceatannol, a Natural Analog of Resveratrol, Inhibits Progression through the S Phase of the Cell Cycle in Colorectal Cancer Cell Lines
Piceatannol, a naturally occurring analog of resveratrol, was previously identified as the active ingredient in herbal preparations in folk medicine and as an inhibitor of p72Syk. We studied the effects of piceatannol on growth, proliferation, differentiation and cell cycle distribution profile of t...
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Veröffentlicht in: | The Journal of nutrition 2002-02, Vol.132 (2), p.298-302 |
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description | Piceatannol, a naturally occurring analog of resveratrol, was previously identified as the active ingredient in herbal preparations in folk medicine and as an inhibitor of p72Syk. We studied the effects of piceatannol on growth, proliferation, differentiation and cell cycle distribution profile of the human colon carcinoma cell line Caco-2. Growth of Caco-2 and HCT-116 cells was analyzed by crystal violet assay, which demonstrated dose- and time-dependent decreases in cell numbers. Treatment of Caco-2 cells with piceatannol reduced proliferation rate. No effect on differentiation was observed. Determination of cell cycle distribution by flow cytometry revealed an accumulation of cells in the S phase. Immunoblotting demonstrated that cyclin-dependent kinases (cdk) 2 and 6, as well as cdc2 were expressed at steady-state levels, whereas cyclin D1, cyclin B1 and cdk 4 were downregulated. The abundance of p27Kip1 was also reduced, whereas the protein level of cyclin E was enhanced. Cyclin A levels were enhanced only at concentrations up to 100 μmol/L. These changes also were observed in studies with HCT-116 cells. On the basis of our findings, piceatannol can be considered to be a promising chemopreventive or anticancer agent. |
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We studied the effects of piceatannol on growth, proliferation, differentiation and cell cycle distribution profile of the human colon carcinoma cell line Caco-2. Growth of Caco-2 and HCT-116 cells was analyzed by crystal violet assay, which demonstrated dose- and time-dependent decreases in cell numbers. Treatment of Caco-2 cells with piceatannol reduced proliferation rate. No effect on differentiation was observed. Determination of cell cycle distribution by flow cytometry revealed an accumulation of cells in the S phase. Immunoblotting demonstrated that cyclin-dependent kinases (cdk) 2 and 6, as well as cdc2 were expressed at steady-state levels, whereas cyclin D1, cyclin B1 and cdk 4 were downregulated. The abundance of p27Kip1 was also reduced, whereas the protein level of cyclin E was enhanced. Cyclin A levels were enhanced only at concentrations up to 100 μmol/L. These changes also were observed in studies with HCT-116 cells. On the basis of our findings, piceatannol can be considered to be a promising chemopreventive or anticancer agent.</description><identifier>ISSN: 0022-3166</identifier><identifier>EISSN: 1541-6100</identifier><identifier>DOI: 10.1093/jn/132.2.298</identifier><identifier>PMID: 11823594</identifier><identifier>CODEN: JONUAI</identifier><language>eng</language><publisher>Bethesda, MD: Elsevier Inc</publisher><subject>Alkaline Phosphatase - metabolism ; Antineoplastic Agents - pharmacology ; Biological and medical sciences ; Blotting, Western ; Caco-2 Cells ; cell cycle ; Cell Cycle - drug effects ; Cell Division ; Cells ; colon cancer ; Colorectal cancer ; Colorectal Neoplasms - drug therapy ; Colorectal Neoplasms - metabolism ; Cyclin-Dependent Kinases - metabolism ; Cyclins - drug effects ; Cyclins - metabolism ; Dose-Response Relationship, Drug ; Flow Cytometry ; Herbs ; Humans ; Nutrition ; piceatannol ; S Phase - drug effects ; Stilbenes - pharmacology ; Time Factors ; Tumor Cells, Cultured</subject><ispartof>The Journal of nutrition, 2002-02, Vol.132 (2), p.298-302</ispartof><rights>2002 American Society for Nutrition.</rights><rights>2002 INIST-CNRS</rights><rights>Copyright American Institute of Nutrition Feb 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c429t-2ff564fcf7d5c4aa382e366a78986371ad29f713d4d92c692a1afe8ece62bf83</citedby><cites>FETCH-LOGICAL-c429t-2ff564fcf7d5c4aa382e366a78986371ad29f713d4d92c692a1afe8ece62bf83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=13481116$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/11823594$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Wolter, Freya</creatorcontrib><creatorcontrib>Clausnitzer, Antje</creatorcontrib><creatorcontrib>Akoglu, Bora</creatorcontrib><creatorcontrib>Stein, Jürgen</creatorcontrib><title>Piceatannol, a Natural Analog of Resveratrol, Inhibits Progression through the S Phase of the Cell Cycle in Colorectal Cancer Cell Lines</title><title>The Journal of nutrition</title><addtitle>J Nutr</addtitle><description>Piceatannol, a naturally occurring analog of resveratrol, was previously identified as the active ingredient in herbal preparations in folk medicine and as an inhibitor of p72Syk. We studied the effects of piceatannol on growth, proliferation, differentiation and cell cycle distribution profile of the human colon carcinoma cell line Caco-2. Growth of Caco-2 and HCT-116 cells was analyzed by crystal violet assay, which demonstrated dose- and time-dependent decreases in cell numbers. Treatment of Caco-2 cells with piceatannol reduced proliferation rate. No effect on differentiation was observed. Determination of cell cycle distribution by flow cytometry revealed an accumulation of cells in the S phase. Immunoblotting demonstrated that cyclin-dependent kinases (cdk) 2 and 6, as well as cdc2 were expressed at steady-state levels, whereas cyclin D1, cyclin B1 and cdk 4 were downregulated. The abundance of p27Kip1 was also reduced, whereas the protein level of cyclin E was enhanced. Cyclin A levels were enhanced only at concentrations up to 100 μmol/L. These changes also were observed in studies with HCT-116 cells. On the basis of our findings, piceatannol can be considered to be a promising chemopreventive or anticancer agent.</description><subject>Alkaline Phosphatase - metabolism</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Biological and medical sciences</subject><subject>Blotting, Western</subject><subject>Caco-2 Cells</subject><subject>cell cycle</subject><subject>Cell Cycle - drug effects</subject><subject>Cell Division</subject><subject>Cells</subject><subject>colon cancer</subject><subject>Colorectal cancer</subject><subject>Colorectal Neoplasms - drug therapy</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Cyclin-Dependent Kinases - metabolism</subject><subject>Cyclins - drug effects</subject><subject>Cyclins - metabolism</subject><subject>Dose-Response Relationship, Drug</subject><subject>Flow Cytometry</subject><subject>Herbs</subject><subject>Humans</subject><subject>Nutrition</subject><subject>piceatannol</subject><subject>S Phase - drug effects</subject><subject>Stilbenes - pharmacology</subject><subject>Time Factors</subject><subject>Tumor Cells, Cultured</subject><issn>0022-3166</issn><issn>1541-6100</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkU1rGzEQhkVpaVy3t56LKKSnONHXaqVjWPoRMK1pcxeydmTLrKVU2g3kH_RnV4sNgVLmMIh59M7wvgi9p-SaEs1vDvGGcnZdS6sXaEEbQVeSEvISLQhhbMWplBfoTSkHQggVWr1GF5QqxhstFujPJjiwo40xDVfY4u92nLId8G20Q9rh5PFPKI-Q7Zhn4C7uwzaMBW9y2mUoJaSIx31O025fO-BfeLO3BeaP87ODYcDdkxsAh4i7NKQMbqz6nY0O8mm-DhHKW_TK26HAu3Nfovsvn--7b6v1j6933e165QTT44p530jhnW_7xglruWLApbSt0kryltqead9S3oteMyc1s9R6UOBAsq1XfIk-nWQfcvo9QRnNMRRXr7AR0lRMSwVXTTuDH_8BD2nK1ZViqG4Fl7TuW6KrE-RyKiWDNw85HG1-MpSYOR1ziKamY2rpWfPDWXPaHqF_hs9xVODyDNji7OBzdSmUZ44LRSmd98oTB9WpxwDZFBegOtqH2V_Tp_D_C_4C-iSqCg</recordid><startdate>20020201</startdate><enddate>20020201</enddate><creator>Wolter, Freya</creator><creator>Clausnitzer, Antje</creator><creator>Akoglu, Bora</creator><creator>Stein, Jürgen</creator><general>Elsevier Inc</general><general>American Society for Nutritional Sciences</general><general>American Institute of Nutrition</general><scope>6I.</scope><scope>AAFTH</scope><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>K9.</scope><scope>NAPCQ</scope><scope>7X8</scope></search><sort><creationdate>20020201</creationdate><title>Piceatannol, a Natural Analog of Resveratrol, Inhibits Progression through the S Phase of the Cell Cycle in Colorectal Cancer Cell Lines</title><author>Wolter, Freya ; Clausnitzer, Antje ; Akoglu, Bora ; Stein, Jürgen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c429t-2ff564fcf7d5c4aa382e366a78986371ad29f713d4d92c692a1afe8ece62bf83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Alkaline Phosphatase - metabolism</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Biological and medical sciences</topic><topic>Blotting, Western</topic><topic>Caco-2 Cells</topic><topic>cell cycle</topic><topic>Cell Cycle - drug effects</topic><topic>Cell Division</topic><topic>Cells</topic><topic>colon cancer</topic><topic>Colorectal cancer</topic><topic>Colorectal Neoplasms - drug therapy</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Cyclin-Dependent Kinases - metabolism</topic><topic>Cyclins - drug effects</topic><topic>Cyclins - metabolism</topic><topic>Dose-Response Relationship, Drug</topic><topic>Flow Cytometry</topic><topic>Herbs</topic><topic>Humans</topic><topic>Nutrition</topic><topic>piceatannol</topic><topic>S Phase - drug effects</topic><topic>Stilbenes - pharmacology</topic><topic>Time Factors</topic><topic>Tumor Cells, Cultured</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wolter, Freya</creatorcontrib><creatorcontrib>Clausnitzer, Antje</creatorcontrib><creatorcontrib>Akoglu, Bora</creatorcontrib><creatorcontrib>Stein, Jürgen</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Premium</collection><collection>MEDLINE - Academic</collection><jtitle>The Journal of nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wolter, Freya</au><au>Clausnitzer, Antje</au><au>Akoglu, Bora</au><au>Stein, Jürgen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Piceatannol, a Natural Analog of Resveratrol, Inhibits Progression through the S Phase of the Cell Cycle in Colorectal Cancer Cell Lines</atitle><jtitle>The Journal of nutrition</jtitle><addtitle>J Nutr</addtitle><date>2002-02-01</date><risdate>2002</risdate><volume>132</volume><issue>2</issue><spage>298</spage><epage>302</epage><pages>298-302</pages><issn>0022-3166</issn><eissn>1541-6100</eissn><coden>JONUAI</coden><abstract>Piceatannol, a naturally occurring analog of resveratrol, was previously identified as the active ingredient in herbal preparations in folk medicine and as an inhibitor of p72Syk. We studied the effects of piceatannol on growth, proliferation, differentiation and cell cycle distribution profile of the human colon carcinoma cell line Caco-2. Growth of Caco-2 and HCT-116 cells was analyzed by crystal violet assay, which demonstrated dose- and time-dependent decreases in cell numbers. Treatment of Caco-2 cells with piceatannol reduced proliferation rate. No effect on differentiation was observed. Determination of cell cycle distribution by flow cytometry revealed an accumulation of cells in the S phase. Immunoblotting demonstrated that cyclin-dependent kinases (cdk) 2 and 6, as well as cdc2 were expressed at steady-state levels, whereas cyclin D1, cyclin B1 and cdk 4 were downregulated. The abundance of p27Kip1 was also reduced, whereas the protein level of cyclin E was enhanced. Cyclin A levels were enhanced only at concentrations up to 100 μmol/L. These changes also were observed in studies with HCT-116 cells. 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subjects | Alkaline Phosphatase - metabolism Antineoplastic Agents - pharmacology Biological and medical sciences Blotting, Western Caco-2 Cells cell cycle Cell Cycle - drug effects Cell Division Cells colon cancer Colorectal cancer Colorectal Neoplasms - drug therapy Colorectal Neoplasms - metabolism Cyclin-Dependent Kinases - metabolism Cyclins - drug effects Cyclins - metabolism Dose-Response Relationship, Drug Flow Cytometry Herbs Humans Nutrition piceatannol S Phase - drug effects Stilbenes - pharmacology Time Factors Tumor Cells, Cultured |
title | Piceatannol, a Natural Analog of Resveratrol, Inhibits Progression through the S Phase of the Cell Cycle in Colorectal Cancer Cell Lines |
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