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来自海洋源白色链霉菌的棘孢菌素作为新型细胞周期抑制剂和凋亡诱导剂。

Echinosporins as new cell cycle inhibitors and apoptosis inducers from marine-derived Streptomyces albogriseolus.

作者信息

Cui C B, Liu H B, Gu J Y, Gu Q Q, Cai B, Zhang D Y, Zhu T J

机构信息

Key Laboratory of Marine Drugs, Chinese Ministry of Education, Institute of Marine Drugs and Foods, Ocean University of China, Qingdao 266003, PR China.

出版信息

Fitoterapia. 2007 Apr;78(3):238-40. doi: 10.1016/j.fitote.2006.11.017. Epub 2007 Feb 6.

DOI:10.1016/j.fitote.2006.11.017
PMID:17376609
Abstract

Bioassay-guided fractionation of the ethyl acetate extract from the fermentation broth of marine-derived Streptomyces albogriseolus A2002 led to the isolation of echinosporin (1) and 7-deoxyechinosporin (2). Compound 1 inhibited the proliferation of tsFT210, K562 and HCT-15 cancer cells (IC(50) 91.5 microM, 25.1 microM and 247 microM respectively) and 2 showed the same effect on K562 cells (IC(50) 143 microM). Flow cytometric analysis suggested that 1 and 2 exert their anti-proliferative effects on those cells through inhibiting cell cycle at the G(2)/M phase and inducing apoptosis.

摘要

对海洋来源的白灰链霉菌A2002发酵液乙酸乙酯提取物进行生物活性导向的分离,得到了刺孢霉素(1)和7-脱氧刺孢霉素(2)。化合物1抑制tsFT210、K562和HCT-15癌细胞的增殖(IC50分别为91.5 microM、25.1 microM和247 microM),化合物2对K562细胞显示出相同的作用(IC50为143 microM)。流式细胞术分析表明,1和2通过在G2/M期抑制细胞周期和诱导凋亡对这些细胞发挥抗增殖作用。

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