Radicicol leads to selective depletion of Raf kinase and disrupts K-Ras-activated aberrant signaling pathway

被引:96
作者
Soga, S
Kozawa, T
Narumi, H
Akinaga, S
Irie, K
Matsumoto, K
Sharma, SV
Nakano, H
Mizukami, T
Hara, M
机构
[1] Kyowa Hakko Kogyo Co Ltd, Tokyo Res Labs, Machida, Tokyo 194, Japan
[2] Kyowa Hakko Kogyo Co Ltd, Pharmaceut Res Labs, Nagaizumi, Shizuoka 411, Japan
[3] Nagoya Univ, Fac Sci, Dept Mol Biol, Chikusa Ku, Nagoya, Aichi 46401, Japan
[4] Univ Tennessee, Ctr Hlth Sci, Dept Microbiol & Immunol, Memphis, TN 38163 USA
关键词
D O I
10.1074/jbc.273.2.822
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Activation of Ras leads to the constitutive activation of a downstream phosphorylation cascade comprised of Raf-1, mitogen-activated protein kinase (MAPK) kinase, and MAPK, We have developed a yeast-based assay in which the Saccharomyces cerevisiae mating pheromone-induced MAPK pathway relied on co-expression of K-Ras and Raf-1, Radicicol, an antifungal antibiotic, was found to inhibit the K-ras signaling pathway reconstituted in yeast, In K-ras-transformed, rat epithelial, and K-ras-activated, human pancreatic carcinoma cell lines, radicicol inhibited K Ras-induced hyperphosphorylation of Erk2, In addition, the level of Raf kinase was significantly decreased in radicicol-treated cells, whereas the levels of K-Ras and MAPK remained unchanged, These results suggest that radicicol disrupts the K-Ras-activated signaling pathway by selectively depleting Raf kinase and raises the possibility that pharmacological destabilization of Raf kinase could be a new and powerful approach for the treatment of K-ras-activated human cancers.
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收藏
页码:822 / 828
页数:7
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