Geranylgeranylacetone inhibits ovarian cancer progression in vitro and in vivo

被引:11
|
作者
Hashimoto, Kae
Morishige, Ken-ichirou
Sawada, Kenjiro
Ogata, Seiji
Tahara, Masahiro
Shimizu, Shoko
Sakata, Masahiro
Tasaka, Keiichi
Kimura, Tadashi
机构
[1] Osaka Univ, Grad Sch Med, Dept Obstet & Gynecol, Suita, Osaka, Japan
[2] Univ Chicago, Div Gynecol Oncol, Dept Obstet & Gynecol, Chicago, IL 60637 USA
关键词
geranylgeranylacetone; lysophosphatidic acid; Rho; Ras; geranylgeranylation; ovarian cancer;
D O I
10.1016/j.bbrc.2007.02.102
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
Geranylgeranylacetone (GGA), an isoprenoid compound, is an anti-ulcer drug developed in Japan. In our previous study, GGA was shown to inhibit ovarian cancer invasion by attenuating Rho activation [K. Hashimoto, K. Morishige, K. Sawada, M. Tahara, S. Shimizu, M. Sakata, K. Tasaka, Y. Murata, Geranylgeranylacetone inhibits lysophosphatidic acid-induced invasion of human ovarian carcinoma cells in vitro. Cancer 103 (2005) 1529-1536]. In the present study, GGA treatment inhibited ovarian cancer progression in vitro and suppressed the tumor growth and ascites in the in vivo ovarian cancer model. In vitro analysis, treatment of cancer cells by GGA resulted in the inhibition of cancer cell proliferation, the inactivation of Ras, and the suppression of tyrosine phosphorylation of mitogen-activated protein kinase (MAPK). In conclusion, this is the first report that GGA inhibited ovarian cancer progression and the antitumor effect by GGA is, at least in part, derived not only from the suppression of Rho activation but also Ras-MAPK activation. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:72 / 77
页数:6
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