Annonacin, a mono-tetrahydrofuran acetogenin, arrests cancer cells at the G1 phase and causes cytotoxicity in a Bax- and caspase-3-related pathway

被引:86
作者
Yuan, SSF
Chang, HL
Chen, HW
Yeh, YT
Kao, YH
Lin, KH
Wu, YC
Su, JH
机构
[1] Kaohsiung Med Univ, Dept Obstet & Gynecol, Kaohsiung 807, Taiwan
[2] Kaohsiung Med Univ, Grad Inst Nat Prod, Kaohsiung 807, Taiwan
[3] Chang Gung Univ, Chang Gung Mem Hosp, Dept Surg, Div Urol, Taipei, Taiwan
[4] Kaohsiung Med Univ, Dept Dermatol, Kaohsiung 807, Taiwan
[5] Kaohsiung Med Univ, Dept Clin Lab, Kaohsiung 807, Taiwan
关键词
annonaceae; Annona reticulata; acetogenins; annonacin; cytotoxicity; apoptosis; cell cycle checkpoints;
D O I
10.1016/S0024-3205(03)00190-5
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Annonaceous acetogenins are a group of potential anti-neoplastic agents isolated from Annonaceae plants. In this study, we purified annonacin, a cytotoxic mono-tetrahydrofuran acetogenin, from the seeds of Annona reticulata and analyzed its biological effects. Herein, we have shown that annonacin caused significant cell death in various cancer cell lines. T24 bladder cancer cells at the S phase were more vulnerable to the cytotoxicity of annonacin. Furthermore, annonacin activated p21 in a p53-independent manner and arrested T24 cells at the G1 phase. It also induced Bax expression, enhanced caspase-3 activity, and caused apoptotic cell death in T24 cells. In summary, these results suggest that annonacin is potentially a promising anti-cancer compound. (C) 2003 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:2853 / 2861
页数:9
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