Isoliquiritigenin inhibits the growth of prostate cancer

被引:175
作者
Kanazawa, M [1 ]
Satomi, Y
Mizutani, Y
Ukimura, O
Kawauchi, A
Sakai, T
Baba, M
Okuyama, T
Nishino, H
Miki, T
机构
[1] Kyoto Prefectural Univ Med, Dept Urol, Kyoto 6028566, Japan
[2] Kyoto Prefectural Univ Med, Dept Biochem, Kyoto, Japan
[3] Kyoto Prefectural Univ Med, Dept Prevent Med, Kyoto, Japan
[4] Meiji Pharmaceut Univ, Dept Nat Med & Phytochem, Tokyo, Japan
关键词
prostate cancer; isoliquiritigenin; GADD153; cell cycle arrest;
D O I
10.1016/S0302-2838(03)00090-3
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objective: Isoliquiritigenin, one of the components in the root of Glycyrrhiza glabra L., is a member of the flavonoids, which are known to have an anti-tumor activity in vitro and in vivo. In this study, we investigated the antitumor effect of isoliquiritigenin on prostate cancer in vitro. Methods: DU145 and LNCaP prostate cancer cell lines were used as targets. We examined the effects of isoliquiritigenin on cell proliferation, cell cycle regulation and cell cycle-regulating gene expression. Further, we investigated the effects of isoliquiritigenin on the GADD153 mRNA and protein expression, and promoter activity. Results: Isoliquiritigenin significantly inhibited the proliferation of prostate cancer cell lines in a dose-dependent and time-dependent manner. Fluorescence-activated cell sorting (FAGS) analysis indicated that isoliquiritigenin induced S and G2/M phase arrest. Isoliquiritigenin enhanced the expression of GADD153 mRNA and protein associated with cell cycle arrest. Further, isoliquiritigenin stimulated transcriptional activity of GADD153 promoter dose-dependently. Conclusion: These findings suggest that isoliquiritigenin is a candidate agent for the treatment of prostate cancer and GADD153 may play an important role in isoliquiritigenin-induced cell cycle arrest and cell growth inhibition. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:580 / 586
页数:7
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