Topoisomerase II-Targeting Properties of a Grapevine-Shoot Extract and Resveratrol Oligomers
Grapevine-shoot extracts (GSE), containing trans-resveratrol and resveratrol oligomers, are commercially available as food supplements. Considering the topoisomerase-targeting properties of trans-resveratrol, the question of whether GSE affect these enzymes, thereby potentially causing DNA damage, w...
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Veröffentlicht in: | Journal of agricultural and food chemistry 2014-01, Vol.62 (3), p.780-788 |
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creator | Baechler, Simone A Schroeter, Anika Dicker, Martina Steinberg, Pablo Marko, Doris |
description | Grapevine-shoot extracts (GSE), containing trans-resveratrol and resveratrol oligomers, are commercially available as food supplements. Considering the topoisomerase-targeting properties of trans-resveratrol, the question of whether GSE affect these enzymes, thereby potentially causing DNA damage, was addressed. In a decatenation assay, GSE potently suppressed the catalytic activity of topoisomerase IIα (≥5 μg/mL). The resveratrol oligomers ε-viniferin, r2-viniferin, and hopeaphenol, isolated from GSE, were also identified as topoisomerase IIα inhibitors. In the in vivo complexes of enzyme to DNA (ICE) bioassay, neither GSE, r2-viniferin, nor hopeaphenol affected the level of enzyme–DNA intermediates in A431 cells, thus representing catalytic inhibitors rather than topoisomerase poisons. GSE caused moderate DNA strand breaks (≥25 μg/mL) in the comet assay. Taken together, GSE presumably acts as a catalytic inhibitor of topoisomerase II with r2-viniferin and hopeaphenol as potentially contributing constituents. However, the increase of FPG-sensitive sites points to an additional mechanism that may contribute to the DNA-damaging properties of GSE constituents. |
doi_str_mv | 10.1021/jf4046182 |
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Considering the topoisomerase-targeting properties of trans-resveratrol, the question of whether GSE affect these enzymes, thereby potentially causing DNA damage, was addressed. In a decatenation assay, GSE potently suppressed the catalytic activity of topoisomerase IIα (≥5 μg/mL). The resveratrol oligomers ε-viniferin, r2-viniferin, and hopeaphenol, isolated from GSE, were also identified as topoisomerase IIα inhibitors. In the in vivo complexes of enzyme to DNA (ICE) bioassay, neither GSE, r2-viniferin, nor hopeaphenol affected the level of enzyme–DNA intermediates in A431 cells, thus representing catalytic inhibitors rather than topoisomerase poisons. GSE caused moderate DNA strand breaks (≥25 μg/mL) in the comet assay. Taken together, GSE presumably acts as a catalytic inhibitor of topoisomerase II with r2-viniferin and hopeaphenol as potentially contributing constituents. However, the increase of FPG-sensitive sites points to an additional mechanism that may contribute to the DNA-damaging properties of GSE constituents.</description><identifier>ISSN: 0021-8561</identifier><identifier>EISSN: 1520-5118</identifier><identifier>DOI: 10.1021/jf4046182</identifier><identifier>PMID: 24369070</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Antigens, Neoplasm - metabolism ; bioassays ; Biocatalysis - drug effects ; catalytic activity ; Cell Line, Tumor ; Comet Assay ; dietary supplements ; DNA ; DNA damage ; DNA Damage - drug effects ; DNA topoisomerase (ATP-hydrolysing) ; DNA Topoisomerases, Type II - metabolism ; DNA-Binding Proteins - antagonists & inhibitors ; DNA-Binding Proteins - metabolism ; Enzyme Inhibitors - chemistry ; Enzyme Inhibitors - pharmacology ; Humans ; Plant Extracts - chemistry ; Plant Extracts - pharmacology ; Plant Shoots - chemistry ; resveratrol ; Stilbenes - chemistry ; Stilbenes - pharmacology ; viniferins ; Vitis - chemistry</subject><ispartof>Journal of agricultural and food chemistry, 2014-01, Vol.62 (3), p.780-788</ispartof><rights>Copyright © 2013 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a254t-7951a869267ce230ffd85da59c68a453fa054f4b2c4bdef49b2ae52eadc974413</citedby><cites>FETCH-LOGICAL-a254t-7951a869267ce230ffd85da59c68a453fa054f4b2c4bdef49b2ae52eadc974413</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/jf4046182$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/jf4046182$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24369070$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baechler, Simone A</creatorcontrib><creatorcontrib>Schroeter, Anika</creatorcontrib><creatorcontrib>Dicker, Martina</creatorcontrib><creatorcontrib>Steinberg, Pablo</creatorcontrib><creatorcontrib>Marko, Doris</creatorcontrib><title>Topoisomerase II-Targeting Properties of a Grapevine-Shoot Extract and Resveratrol Oligomers</title><title>Journal of agricultural and food chemistry</title><addtitle>J. Agric. Food Chem</addtitle><description>Grapevine-shoot extracts (GSE), containing trans-resveratrol and resveratrol oligomers, are commercially available as food supplements. Considering the topoisomerase-targeting properties of trans-resveratrol, the question of whether GSE affect these enzymes, thereby potentially causing DNA damage, was addressed. In a decatenation assay, GSE potently suppressed the catalytic activity of topoisomerase IIα (≥5 μg/mL). The resveratrol oligomers ε-viniferin, r2-viniferin, and hopeaphenol, isolated from GSE, were also identified as topoisomerase IIα inhibitors. In the in vivo complexes of enzyme to DNA (ICE) bioassay, neither GSE, r2-viniferin, nor hopeaphenol affected the level of enzyme–DNA intermediates in A431 cells, thus representing catalytic inhibitors rather than topoisomerase poisons. GSE caused moderate DNA strand breaks (≥25 μg/mL) in the comet assay. Taken together, GSE presumably acts as a catalytic inhibitor of topoisomerase II with r2-viniferin and hopeaphenol as potentially contributing constituents. However, the increase of FPG-sensitive sites points to an additional mechanism that may contribute to the DNA-damaging properties of GSE constituents.</description><subject>Antigens, Neoplasm - metabolism</subject><subject>bioassays</subject><subject>Biocatalysis - drug effects</subject><subject>catalytic activity</subject><subject>Cell Line, Tumor</subject><subject>Comet Assay</subject><subject>dietary supplements</subject><subject>DNA</subject><subject>DNA damage</subject><subject>DNA Damage - drug effects</subject><subject>DNA topoisomerase (ATP-hydrolysing)</subject><subject>DNA Topoisomerases, Type II - metabolism</subject><subject>DNA-Binding Proteins - antagonists & inhibitors</subject><subject>DNA-Binding Proteins - metabolism</subject><subject>Enzyme Inhibitors - chemistry</subject><subject>Enzyme Inhibitors - pharmacology</subject><subject>Humans</subject><subject>Plant Extracts - chemistry</subject><subject>Plant Extracts - pharmacology</subject><subject>Plant Shoots - chemistry</subject><subject>resveratrol</subject><subject>Stilbenes - chemistry</subject><subject>Stilbenes - pharmacology</subject><subject>viniferins</subject><subject>Vitis - chemistry</subject><issn>0021-8561</issn><issn>1520-5118</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpt0LFOwzAQBmALgWgpDLwAeGFgCJwdO3FGVJVSCamIthtSdEnskKqNIzut4O1JFejEdMN9-k_3E3LN4IEBZ49rI0BETPETMmSSQyAZU6dkCN0yUDJiA3Lh_RoAlIzhnAy4CKMEYhiSj6VtbOXtVjv0ms5mwRJdqduqLumbs412baU9tYYinTps9L6qdbD4tLalk6_WYd5SrAv6rv2-i2id3dD5pioPgf6SnBnceH31O0dk9TxZjl-C1_l0Nn56DZBL0QZxIhmqKOFRnGsegjGFkgXKJI8UChkaBCmMyHguskIbkWQcteQaizyJhWDhiNz3ubmz3jtt0sZVW3TfKYP00FB6bKizN71tdtlWF0f5V0kHbntg0KZYusqnqwUHJgCYYnGiOnHXC8x9urY7V3fP_XPqB1EUdoA</recordid><startdate>20140122</startdate><enddate>20140122</enddate><creator>Baechler, Simone A</creator><creator>Schroeter, Anika</creator><creator>Dicker, Martina</creator><creator>Steinberg, Pablo</creator><creator>Marko, Doris</creator><general>American Chemical Society</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></search><sort><creationdate>20140122</creationdate><title>Topoisomerase II-Targeting Properties of a Grapevine-Shoot Extract and Resveratrol Oligomers</title><author>Baechler, Simone A ; Schroeter, Anika ; Dicker, Martina ; Steinberg, Pablo ; Marko, Doris</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a254t-7951a869267ce230ffd85da59c68a453fa054f4b2c4bdef49b2ae52eadc974413</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Antigens, Neoplasm - metabolism</topic><topic>bioassays</topic><topic>Biocatalysis - drug effects</topic><topic>catalytic activity</topic><topic>Cell Line, Tumor</topic><topic>Comet Assay</topic><topic>dietary supplements</topic><topic>DNA</topic><topic>DNA damage</topic><topic>DNA Damage - drug effects</topic><topic>DNA topoisomerase (ATP-hydrolysing)</topic><topic>DNA Topoisomerases, Type II - metabolism</topic><topic>DNA-Binding Proteins - antagonists & inhibitors</topic><topic>DNA-Binding Proteins - metabolism</topic><topic>Enzyme Inhibitors - chemistry</topic><topic>Enzyme Inhibitors - pharmacology</topic><topic>Humans</topic><topic>Plant Extracts - chemistry</topic><topic>Plant Extracts - pharmacology</topic><topic>Plant Shoots - chemistry</topic><topic>resveratrol</topic><topic>Stilbenes - chemistry</topic><topic>Stilbenes - pharmacology</topic><topic>viniferins</topic><topic>Vitis - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baechler, Simone A</creatorcontrib><creatorcontrib>Schroeter, Anika</creatorcontrib><creatorcontrib>Dicker, Martina</creatorcontrib><creatorcontrib>Steinberg, Pablo</creatorcontrib><creatorcontrib>Marko, Doris</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><jtitle>Journal of agricultural and food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baechler, Simone A</au><au>Schroeter, Anika</au><au>Dicker, Martina</au><au>Steinberg, Pablo</au><au>Marko, Doris</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Topoisomerase II-Targeting Properties of a Grapevine-Shoot Extract and Resveratrol Oligomers</atitle><jtitle>Journal of agricultural and food chemistry</jtitle><addtitle>J. Agric. Food Chem</addtitle><date>2014-01-22</date><risdate>2014</risdate><volume>62</volume><issue>3</issue><spage>780</spage><epage>788</epage><pages>780-788</pages><issn>0021-8561</issn><eissn>1520-5118</eissn><abstract>Grapevine-shoot extracts (GSE), containing trans-resveratrol and resveratrol oligomers, are commercially available as food supplements. Considering the topoisomerase-targeting properties of trans-resveratrol, the question of whether GSE affect these enzymes, thereby potentially causing DNA damage, was addressed. In a decatenation assay, GSE potently suppressed the catalytic activity of topoisomerase IIα (≥5 μg/mL). The resveratrol oligomers ε-viniferin, r2-viniferin, and hopeaphenol, isolated from GSE, were also identified as topoisomerase IIα inhibitors. In the in vivo complexes of enzyme to DNA (ICE) bioassay, neither GSE, r2-viniferin, nor hopeaphenol affected the level of enzyme–DNA intermediates in A431 cells, thus representing catalytic inhibitors rather than topoisomerase poisons. GSE caused moderate DNA strand breaks (≥25 μg/mL) in the comet assay. Taken together, GSE presumably acts as a catalytic inhibitor of topoisomerase II with r2-viniferin and hopeaphenol as potentially contributing constituents. However, the increase of FPG-sensitive sites points to an additional mechanism that may contribute to the DNA-damaging properties of GSE constituents.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>24369070</pmid><doi>10.1021/jf4046182</doi><tpages>9</tpages></addata></record> |
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subjects | Antigens, Neoplasm - metabolism bioassays Biocatalysis - drug effects catalytic activity Cell Line, Tumor Comet Assay dietary supplements DNA DNA damage DNA Damage - drug effects DNA topoisomerase (ATP-hydrolysing) DNA Topoisomerases, Type II - metabolism DNA-Binding Proteins - antagonists & inhibitors DNA-Binding Proteins - metabolism Enzyme Inhibitors - chemistry Enzyme Inhibitors - pharmacology Humans Plant Extracts - chemistry Plant Extracts - pharmacology Plant Shoots - chemistry resveratrol Stilbenes - chemistry Stilbenes - pharmacology viniferins Vitis - chemistry |
title | Topoisomerase II-Targeting Properties of a Grapevine-Shoot Extract and Resveratrol Oligomers |
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