Santonin-related compound 2 inhibits the expression of ICAM-1 in response to IL-1 stimulation by blocking the signaling pathway upstream of IκB degradation
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Kawai, S
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Kataoka, T
Sugimoto, H
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机构:Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
Sugimoto, H
Nakamura, A
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机构:Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
Nakamura, A
Kobayashi, T
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机构:Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
Kobayashi, T
Arao, K
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机构:Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
Arao, K
Higuchi, Y
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机构:Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
Higuchi, Y
Ando, M
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Ando, M
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Nagai, K
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[1] Tokyo Inst Technol, Dept Bioengn, Midori Ku, Yokohama, Kanagawa 2268501, Japan
[2] Niigata Univ, Fac Engn, Dept Appl Chem, Niigata 9502181, Japan
Santonin-related compounds (SRCs) were synthesized from the starting material L-alpha-santonin and tested for the biological activity on the expression of intercellular adhesion molecule-1 (ICAM-1) in response to IL-1 stimulation on human adenocarcinoma cells, One of the bromoketone derivatives termed SRC2 [(11S)-2 alpha-bromo-3-oxoeudesmanno-13,6 alpha-lactone] strongly inhibited the ICAM-1 expression at an IC50 value of 5.9 mu M, whereas L-alpha-santonin itself was totally inactive up to 100 mu M The blockage of ICAM-1 expression by SRC2 was not due to the direct inhibition of de novo RNA and protein synthesis, The nuclear translocation of NF-kappa B subunit p65 was markedly prevented by SRC2, Moreover, I kappa B alpha degradation upon IL-1 stimulation was strongly inhibited by SRC2. These observations suggest that SRC2 blocks the IL-1 signaling pathway upstream of I kappa B degradation. (C) 2000 Elsevier Science B.V. All rights reserved.
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页码:129 / 135
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[1]
BAEUERLE PA, 1994, ANNU REV IMMUNOL, V12, P141, DOI 10.1146/annurev.immunol.12.1.141