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자료유형
학술저널
저자정보
Lee, Seung-Min (Department of Biochemistry & Molecular biology, Korea University Medical College) Kim, Ki-Nam (Department of Biochemistry & Molecular biology, Korea University Medical College) Kim, Yu-Ri (Department of Biochemistry & Molecular biology, Korea University Medical College) Kim, Hye-Won (Department of Biochemistry & Molecular biology, Korea University Medical College) Shim, Boo-Im (Department of Biochemistry & Molecular biology, Korea University Medical College) Lee, Seung-Ho (Department of Biochemistry & Molecular biology, Korea University Medical College) Bae, Hak-Soon (Department of Biochemistry & Molecular biology, Korea University Medical College) Kim, In-Kyoung (Department of Biochemistry & Molecular biology, Korea University Medical College) Kim, Meyoung-Kon (Department of Biochemistry & Molecular biology, Korea University Medical College)
저널정보
대한독성유전단백체학회 Molecular & cellular toxicology Molecular & cellular toxicology 제3권 제4호
발행연도
2007.1
수록면
254 - 261 (8page)

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20-O-($\beta$-D-Glucopyranosyl)-20 (S)-protopanaxadiol (IH-901) is one of the major metabolites of ginsenosides from Panax ginseng, and is suggested that IH-901 has been associated with various pharmacological and physiological activities. In this study, we demonstrate that IH-901 induced anti-inflammation in HT-29 human colon adenocarcinoma cells. Our results showed that IH-901 inhibited cell proliferation of HT-29 in a time- and dose-dependent manner. We also found that IH-901 was significantly decreased expression of iNOS compared with non-treated. We observed effect of IH-901 related with inflammatory genes using by cDNA microarray. We were known that the 34 inflammatory genes such as E2F, CDK6, TNF-$\alpha$, and PKC were down-regulated. Thus, these results suggest that IH-901 may have a potential preventive factor to improving cancer induced by chronic inflammation.

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