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海洋植物海刀豆紫檀素抑制人肿瘤细胞NF-κB活化所致细胞毒性和凋亡作用研究

徐岷涓, 黄新苹, 李敏*, 孙婉, 崔景荣, 林文翰   

  1. 北京大学 天然药物及仿生药物国家重点实验室, 北京 100191
  • 收稿日期:2009-06-27 修回日期:2009-10-15 出版日期:2009-11-30 发布日期:2009-11-30
  • 通讯作者: 李敏*

Cytotoxic and pro-apoptotic activities of medicarpin from Canavalia maritima
(Aubl.) via the suppression of NF-κB activation in HeLa cells

Min-Juan Xu, Xin-Ping Huang, Min Li*, Wan Sun, Jing-Rong Cui, Wen-Han Lin   

  1. State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing 100191, China
  • Received:2009-06-27 Revised:2009-10-15 Online:2009-11-30 Published:2009-11-30
  • Contact: Min Li*

摘要: 从海刀豆中首次分离得到三个已知化合物, (-)-medicarpin (PD1), (-)-2-hydroxy-4,9-dimethoxypterocarpan (PD2), 4-hydroxy-3-methoxy-8,9-methylene-dioxy­pterocarpan (PD3), 并探讨PD1对人肿瘤细胞的细胞毒性和诱导细胞凋亡作用。高内涵筛选分析结果表明, 化合物PD1可以抑制NF-κB的活化, 诱导细胞核固缩、改变细胞膜通透性与线粒体膜电势, 抑制肿瘤细胞增殖。

关键词: 紫檀素, 海刀豆, 抗肿瘤, 凋亡, NF-κB, 高内涵筛选

Abstract:

Three known pterocarpin derivatives, (-)-medicarpin (PD1), (-)-2-hydroxy­4,9-dimethoxypterocarpan (PD2), and 4-hydroxy-3-methoxy-8,9-methylene-dioxypterocarpan (PD3) were isolated from Canavalia maritima, for the first time. The cytotoxic and pro-apoptotic activities of (-)-medicarpin in cutured human tumor HeLa cells and its effect on NF-κB activation were investigated. We found that PD1 inhibited NF-κB activation by high content screening analysis, and PD1 exhibited cytotoxicity by SRB assay. In addition, we found that PD1 induced nuclear condensation and increased membrane permeability and mitochondrial transmembrane potential in HeLa cells in a dose and time dependent manner. In conclusion, our data suggested that (-)-medicarpin was capable of inhibiting tumor cell growth in vitro and inducing apoptosis, which might be via the suppression of NF-κB activation.

Key words: Medicarpin, Medicarpin, Canavalia maritime, Canavalia maritime, Anticancer, Anticancer, Apoptosis, Apoptosis, NF-κB, NF-κB, High content screening, High content screening

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Supporting:

Foundation items: National High Technology Development Project (863 Project, Grants No. 2006AA09Z446, 2006AA09Z405 and 2006DFA31100), NSFC (Grants No. 30672607, 30901845) and the Scientific Research Foundation for the Returned Overseas Chinese Scholars, State Education Ministry.
*Corresponding author. Tel.: 86-10-82801161; fax: 86-10-82802724; e-mail: limin@bjmu.edu.cn