Cancer chemopreventive activity of naphthoquinones and their analogs from Avicennia plants

被引:68
作者
Itoigawa, M [1 ]
Ito, C
Tan, HTW
Okuda, M
Tokuda, H
Nishino, H
Furukawa, H
机构
[1] Tokai Gakuen Univ, Miyoshi, Aichi 4700207, Japan
[2] Meijo Univ, Fac Pharm, Tempa Ku, Nagoya, Aichi 4688503, Japan
[3] Natl Univ Singapore, Dept Bot, Singapore 117548, Singapore
[4] Kyoto Prefectural Univ Med, Dept Biochem, Kamigyo Ku, Kyoto 6020841, Japan
关键词
naphthoquinones; cancer chemopreventive agents; anti-tumor-promoting effect; Epstein-Barr virus activation; two-stage mouse skin carcinogenesis; Avicennia plants;
D O I
10.1016/S0304-3835(01)00707-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
As a part of screening studies for cancer chemopreventive agents (anti-tumor promoters), six natural and four synthetic naphthoquinones and five of their analogs were tested for their inhibitory activities against Epstein-Barr virus early antigen activation induced by 12-O-tetradecanoylphorbol-13-acetate in Raji cells. Some of the 1,4-naphthoquinones and their analogs were found to show remarkably potent activities, without showing any cytotoxicity. 1,4-Furanonaphthoquinone (5) and its analog (9) isolated from Avicennia plants (Avicenniaceae), having an alcoholic OH group on the dihydrofuran-ring, displayed the mo st potent activity. Furthermore, avicenol-A (9) exhibited a marked inhibitory effect on mouse skin tumor promotion in an in vivo two-stage carcinogenesis test. The result of the present investigation indicated that some of these 1,4-naphthoquinones and their analogs might be valuable as potent cancer chemopreventive agents. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:135 / 139
页数:5
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