Plaunotol and Geranylgeraniol Induce Caspase-Mediated Apoptosis in Colon Cancer

被引:19
|
作者
Yoshikawa, Naoyuki [1 ,2 ]
Yamada, Jun [3 ]
Tsuno, Nelson H. [3 ]
Okaji, Yurai
Kawai, Kazushige [3 ]
Tsuchiya, Takeshi [3 ]
Yoneyama, Satomi [3 ]
Tanaka, Junichiro [3 ]
Shuno, Yasutaka [3 ]
Nishikawa, Takeshi [3 ]
Nagawa, Hirokazu [3 ]
Oshima, Noriko [2 ]
Takahashi, Koki
机构
[1] Univ Tokyo, Dept Transfus Med, Fac Med, Bunkyo Ku, Tokyo 1138655, Japan
[2] Toho Univ, Div Mol Med, Dept Biomol Sci, Fac Sci, Chiba 2748510, Japan
[3] Univ Tokyo, Dept Surg Oncol, Fac Med, Tokyo 1138655, Japan
关键词
isoprenoids; plaunotol; geranylgeraniol; apoptosis; caspase; colon cancer cell; MEVALONATE SYNTHESIS; HL-60; CELLS; INHIBITION; ACTIVATION; FARNESOL; RATS;
D O I
10.1016/j.jss.2008.04.021
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Plaunotol, a kind of isoprenoid extracted from a Thai medical plant, plau-noi, is structurally similar to geranylgeraniol (GGOH), another isoprenoid reported to exert strong anticancer effects. Recently, we have reported on its inhibitory effects on tumor angiogenesis and direct effects on gastric cancer cells. Here, we aimed to test whether plaunotol could have some therapeutic effect on colon cancer. Materials and methods. Human colon cancer cell line DLD1 was used. Tumor cells were cultured in the presence of plaunotol or GGOH, and their proliferation was measured by MTS assay. Apoptosis was evaluated by Annexin V and propidium iodide double-staining or terminal-deoxynucleotidyl assay. The activation of caspase-3, -8, and -9 was analyzed by flow cytometry and Western blot analysis for PRRP cleavage. Results. Plaunotol and GGOH strongly inhibited the proliferative activity of DLD1, dependent on induction of apoptosis. The induction of apoptosis by either plaunotol or GGOH was dependent on the activation of both caspase-8 and caspase-9 pathways. Conclusions. Plaunotol would be a potential anticancer agent against colon cancer, and since it is already available in Japan and Thailand for clinical use as an anti-ulcer/antigastritis agent, clinical trials will be designed to confirm the present findings. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:246 / 253
页数:8
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