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Issue title: The Proceedings of the 3rd International Conference on Food Factors (ICoFF 03)
Article type: Research Article
Authors: Kim, Sue Ok | Chun, Kyung-Soo | Kundu, Joydeb Kumar | Surh, Young-Joon
Affiliations: College of Pharmacy, Seoul National University, Seoul 151-742, South Korea
Note: [] Address for correspondence: Professor Young-Joon Surh, College of Pharmacy, Seoul National University, Shillim-dong, Kwanak-ku, Seoul 151-742, South Korea. Tel.: +82 2 880 7845; Fax: +82 2 874 9775; E-mail: surh@plaza.snu.ac.kr
Abstract: [6]-Gingerol, a major pungent ingredient of ginger (Zingiber officinale Roscoe, Zingiberaceae), has a wide array of pharmacologic effects. Previous studies have demonstrated that [6]-gingerol inhibits mouse skin tumor promotion and anchorage-independent growth of cultured mouse epidermal cells stimulated with epidermal growth factor. Cyclooxygenase-2 (COX-2), a key enzyme in the prostaglandin biosynthesis, has been recognized as a molecular target for many anti-inflammatory as well as chemopreventive agents. Topical application of [6]-gingerol inhibited phorbol 12-myristate 13-acetate -induced COX-2 expression. One of the essential transcription factors responsible for COX-2 induction is NF-κB. [6]-Gingerol suppressed NF-κB DNA binding activity in mouse skin. In addition, [6]-gingerol inhibited the phoshorylation of p38 mitogen-activated protein kinase which may account for its inactivation of NF-κB and suppression of COX-2 expression.
Keywords: chemoprevention, cyclooxygenase-2, [6]-gingerol, p38 MAPK, NF-κB, mouse skin
Journal: BioFactors, vol. 21, no. 1-4, pp. 27-31, 2004
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