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pubmed-article:20105429pubmed:dateCreated2010-3-9lld:pubmed
pubmed-article:20105429pubmed:abstractTextCancer preventive reagent trans-resveratrol is intracellularly biotransformed to different metabolites. However, it is still unclear whether trans-resveratrol exerts its biological effects directly or through its metabolite(s). This issue was addressed here by identifying the metabolic pattern and the bioactive form of resveratrol in a resveratrol-sensitive human medulloblastoma cell line, UW228-3. The cell lysates and condition media of UW228-3 cells with or without 100 microM resveratrol treatment were analyzed by HPLC and LC/MS which revealed (1) that resveratrol was chemically unstable and the spontaneous generation of cis-resveratrol reduced resveratrol's anti-medulloblastoma efficacy and (2) that resveratrol monosulfate was the major metabolite of the cells. To identify the bioactive form of resveratrol, a mixture-containing approximately half fraction of resveratrol monosulfate was prepared by incubating trans-resveratrol with freshly prepared rat brain lysates. Medulloblastoma cells treated by 100 microM of this mixture showed attenuated cell crisis. The overall levels of the three brain-associated sulfotransferases (SULT1A1, 1C2 and 4A1) were low in medulloblastoma cells in vivo and in vitro in comparison with that in human noncancerous and rat normal cerebella; resveratrol could more or less up-regulate the production of these enzymes in UW228-3 cells but their overall level was still lower than that in normal cerebellum tissue. Our study thus demonstrated for the first time that trans-resveratrol is the bioactive form in medulloblastoma cells in which the expression of brain-associated SULTs was down-regulated, resulting in the increased intracellular bioavailability and anti-medulloblastoma efficacy of trans-resveratrol.lld:pubmed
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pubmed-article:20105429pubmed:authorpubmed-author:LeeL JLJlld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:LiHongHlld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:WangQianQlld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:SunYuanYlld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:KongQing-YouQ...lld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:ChenXiao-YanX...lld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:SunZhengZlld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:WangJian-MinJ...lld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:MaJing-XinJXlld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:ShuXiao-HongX...lld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:WuMo-LiMLlld:pubmed
pubmed-article:20105429pubmed:authorpubmed-author:FuYuan-ShanYSlld:pubmed
pubmed-article:20105429pubmed:copyrightInfo2010 Elsevier Inc. All rights reserved.lld:pubmed
pubmed-article:20105429pubmed:issnTypeElectroniclld:pubmed
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pubmed-article:20105429pubmed:volume79lld:pubmed
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pubmed-article:20105429pubmed:articleTitleIdentification of metabolic pattern and bioactive form of resveratrol in human medulloblastoma cells.lld:pubmed
pubmed-article:20105429pubmed:affiliationDepartment of Cell Biology, Dalian Medical University, China.lld:pubmed
pubmed-article:20105429pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20105429pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed