首页> 美国卫生研究院文献>Advanced Pharmaceutical Bulletin >Two Active Compounds from Caesalpinia sappan L. in Combination with Cisplatin Synergistically Induce Apoptosis and Cell Cycle Arrest on WiDr Cells
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Two Active Compounds from Caesalpinia sappan L. in Combination with Cisplatin Synergistically Induce Apoptosis and Cell Cycle Arrest on WiDr Cells

机译:Ca草中的两种活性化合物与顺铂协同诱导WiDr细胞凋亡和细胞周期阻滞

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摘要

>Purpose: The aim of this study is to observe the synergistic effect of two active compounds of secang, brazilin and brazilein, combined with cisplatin on WiDr colon cancer cells.>Methods: Cytotoxic activities of brazilin (Bi) and brazilein (Be) in single and in combination with cisplatin (Cisp) were examined by MTT assay. Synergistic effect was analyzed by combination index (CI) parameter. Apoptosis and cell cycle profiles were observed by using flow cytometry.>Results: The result of MTT assay showed that IC50 value of brazilin and brazilein on WiDr cancer cells were 41 µM and 52 µM respectively. The combination of ½ IC50 of Bi-Cisp reduced cells viability up to 64% and showed synergistic effect with CI value less than 1 (CI = 0.8). The combinations of ½ IC50 of Be-Cisp also reduced cells viability up to 78% and showed synergistic effect (CI=0.65). Combination of Bi-Cisp and Be-Cisp induced apoptosis higher than the single treatments. Further analysis on the cell cycle progression showed that single treatment of ½ IC50 of Be and Bi induced S-phase and G2/M-phase accumulation, while combination of Be-Cisp and Bi-Cisp enhanced S-phase accumulation.>Conclusion: Both combination of Bi-Cisp and Be-Cisp showed synergistic effect on WiDr cells through induction of apoptosis and halted the cell cycle progression, thus, WiDr cells growth were significantly reduced.
机译:>目的:本研究的目的是观察secang的两种活性化合物巴西青霉素和巴西青霉素联合顺铂对WiDr结肠癌细胞的协同作用。>方法:通过MTT法检测了单药或与顺铂(Cisp)联合使用时,巴西(Bi)和巴西(Be)的活性。通过组合指数(CI)参数分析协同效应。流式细胞术观察细胞凋亡和细胞周期概况。>结果: MTT法检测结果表明,巴西灵和巴西灵对WiDr癌细胞的IC50值分别为41 µM和52 µM。 Bi-Cisp的½IC50的组合将细胞活力降低了64%,并显示出协同效应,CI值小于1(CI = 0.8)。 Be-Cisp的1/2 IC50组合也将细胞活力降低了78%,并表现出协同效应(CI = 0.65)。 Bi-Cisp和Be-Cisp的组合诱导的细胞凋亡高于单一治疗。对细胞周期进程的进一步分析表明,单一处理Be和Bi的½IC50会诱导S期和G2 / M期积累,而Be-Cisp和Bi-Cisp的组合会增强S期积累。>结论: Bi-Cisp和Be-Cisp的组合均通过诱导凋亡而对WiDr细胞产生协同作用,并停止了细胞周期进程,因此,WiDr细胞的生长显着降低。

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