MCF-7乳腺癌细胞中由乙酸木屑和甘露质萃取物结合而成的协同效应

Sari Haryanti, Ika Yanti M. Sholikhah, Y. Widiyastuti
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引用次数: 0

摘要

癌症是一种危重、慢性、复杂的疾病,也是世界上死亡人数最多的疾病。苏木中的Brazilin和brazilein(Caesalpia sappan L.)和苦姜根茎中的泽隆酮(Zingiber zerumbet L.)已知具有不同机制的细胞毒性活性。本研究旨在考察苏木和苦姜的配伍效果。Sappan木和苦姜根状茎用96%乙醇浸渍3x24小时,过滤并蒸发以获得干燥提取物。MTT法检测MCF-7细胞的细胞毒性。CompuSyn根据细胞毒性组合的结果确定组合指数(CI)。流式细胞仪分析细胞周期和细胞凋亡诱导。Sappan木提取物和苦姜根对MCF-7细胞具有细胞毒性作用,IC50分别为30和155μg/mL。苏木15μg/mL与苦姜8、12、24和60μg/mL的组合产生协同效应,CI值为0.57-0.85。15μg/mL Sappan wood与8μg/mL和24μg/mL苦姜组合在G2/M期表现出细胞周期抑制作用。与未处理的细胞及其单一处理相比,该组合还增加了细胞凋亡诱导。苏木乙醇提取物与苦姜根茎的组合显示出协同的细胞毒性作用。其协同作用表现为细胞周期阻滞在G2/M期,加速细胞凋亡诱导。
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Efek Sinergis Kombinasi Ekstrak Etanolik Kayu Secang dan Rimpang Lempuyang pada Sel Kanker Payudara MCF-7
Cancer is one of critical, chronic, and complex disease, also becoming the high cause of death in the world. Brazilin and brazilein in sappan wood (Caesalpinia sappan L.) and zerumbone in bitter ginger rhizome (Zingiber zerumbet L.) are known having cytotoxic activity with different mechanisms. This study aimed to examine combination effect of sappan wood and bitter ginger rhizome. Sappan wood and bitter ginger rhizomes macerated with ethanol 96% for 3x24 hours, filtered, and evaporated to obtain dried extract.Cytotoxic effect on MCF-7 cells was done using MTT assay. Combination Index (CI) was determined by CompuSyn based on the result of cytotoxic combination. Cell cycle profile and apoptosis induction was analyzed by flow cytometry. Sappan wood extracts and bitter ginger rhizome exhibited cytotoxic effects on MCF-7 cells with the IC50 values of 30 and 155 μg/mL respectively. The combination of sappan wood 15 μg/mL and bitter ginger 8, 12, 24, and 60 μg/mL produced synergistic effect with the CI value of 0.57-0.85. Sappan wood 15 μg/mL combined with bitter ginger 8 and 24 μg/mL showed cell cycle inhibition at G2/M phase. The combination also increased apoptosis induction compared to untreated cells and its single treatment.The combination of sappan wood ethanolic extracts and bitter ginger rhizome showed synergistic cytotoxic effect. Its synergism effect revealed through cell cycle arrested at G2/M phase and acceleration of apoptotic induction.
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