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Molecular basis of chemoprevention by resveratrol: NF-κB and AP-1 as potential targets

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dc.contributor.authorKundu, Joydeb Kumar-
dc.contributor.authorSurh, Young-Joon-
dc.date.accessioned2021-01-31T10:20:30Z-
dc.date.available2021-01-31T10:20:30Z-
dc.date.issued2004-11-
dc.identifier.citationMutation Research, Vol.555 No.1-2, pp.65-80-
dc.identifier.issn0027-5107-
dc.identifier.other4112-
dc.identifier.urihttps://hdl.handle.net/10371/172842-
dc.description.abstractRecently, chemoprevention by the use of naturally occurring substances is considered as a priority to reduce the ever-increasing incidence of cancer. The intervention of multistage carcinogenesis by modulating intracellular signaling pathways may provide molecular basis of chemoprevention with a wide variety of dietary phytochemicals. Resveratrol, a red wine polyphenol, has been studied extensively for the chemopreventive activity in the context of its ability to interfere with the multistage carcinogenesis. Numerous intracellular signaling cascades converge with the activation of nuclear factor-kappaB (NF-kappaB) and activator protein-1 (AP-1), which act independently or coordinately to regulate expression of target genes. These ubiquitous eukaryotic transcription factors mediate pleiotropic effects on cellular transformation and tumor promotion. This review aims to update the molecular mechanisms underlying chernoprevention by resveratrol with special focus on its effect on cellular signaling cascades mediated by NF-kappaB and AP-1. (C) 2004 Elsevier B.V. All rights reserved.-
dc.subjectresveratrol-
dc.subjectchemoprevention-
dc.subjectnuclear factor-kappa B (NF-kappa B)-
dc.subjectactivator protein-1 (AP-1)-
dc.subjectcellular signaling-
dc.subjectapoptosis-
dc.subjectcell cycle regulation-
dc.titleMolecular basis of chemoprevention by resveratrol: NF-κB and AP-1 as potential targets-
dc.typeArticle-
dc.contributor.AlternativeAuthor서영준-
dc.identifier.doi10.1016/j.mrfmmm.2004.05.019-
dc.citation.journaltitleMutation Research-
dc.identifier.scopusid2-s2.0-5144223780-
dc.citation.endpage80-
dc.citation.number1-2-
dc.citation.startpage65-
dc.citation.volume555-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S0027510704002829?via%3Dihub-
dc.identifier.rimsid4112-
dc.identifier.sci000224786700006-
dc.contributor.affiliatedAuthorSurh, Young-Joon-
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Graduate School of Convergence Science and Technology (융합과학기술대학원)Dept. of Molecular and Biopharmaceutical Sciences (분자의학 및 바이오제약학과)Journal Papers (저널논문_분자의학 및 바이오제약학과)
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