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1'S-1'-乙酰氧基丁香酚乙酸酯:一种新的针对 MCF-7 人乳腺癌细胞的化疗天然化合物。

1'S-1'-acetoxyeugenol acetate: a new chemotherapeutic natural compound against MCF-7 human breast cancer cells.

机构信息

Dept. of Genetics & Molecular Biology, (ISB), Faculty of Science, University Malaya, 50603 Kuala Lumpur, Wilayah Persekututan, Malaysia.

出版信息

Phytomedicine. 2010 Oct;17(12):935-9. doi: 10.1016/j.phymed.2010.03.011. Epub 2010 Aug 21.

Abstract

Medicinal plants containing active natural compounds have been used as an alternative treatment for cancer patients in many parts of the world especially in Asia (Itharat et al. 2004). In this report, we describe the cytotoxic and apoptotic properties of 1'S-1'-acetoxyeugenol acetate (AEA), an analogue of 1'S-1'-acetoxychavicol acetate (ACA), isolated from the Malaysian ethno-medicinal plant Alpinia conchigera Griff (Zingiberaceae) on human breast cancer cells. Data from MTT cell viability assays indicated that AEA induced both time- and dose-dependent cytotoxicity with an IC(50) value of 14.0 μM within 36 h of treatment on MCF-7 cells, but not in HMEC normal control cells. Both annexin V-FITC/PI flow cytometric analysis and DNA fragmentation assays confirmed that AEA induced cell death via apoptosis. AEA was also found to induce cell cycle arrest in MCF-7 cells at the G(0)/G(1) phase with no adverse cell cycle arrest effects on HMEC normal control cells. It was concluded that AEA isolated from the Malaysian tropical ginger represents a potential chemotherapeutic agent against human breast cancer cells with higher cytotoxicity potency than its analogue, ACA.

摘要

药用植物中含有的活性天然化合物已被用作癌症患者的替代治疗方法,在世界许多地区,尤其是在亚洲(Itharat 等人,2004 年)。在本报告中,我们描述了 1'S-1'-乙酰氧基丁香酚乙酸酯(AEA)的细胞毒性和凋亡特性,AEA 是 1'S-1'-乙酰氧基黄樟素乙酸酯(ACA)的类似物,从马来西亚民族药用植物 Alpinia conchigera Griff(姜科)中分离出来,作用于人类乳腺癌细胞。MTT 细胞活力测定数据表明,AEA 诱导 MCF-7 细胞在 36 小时内呈时间和剂量依赖性细胞毒性,IC50 值为 14.0 μM,但对 HMEC 正常对照细胞没有作用。 Annexin V-FITC/PI 流式细胞术分析和 DNA 片段化分析均证实 AEA 通过细胞凋亡诱导细胞死亡。AEA 还被发现诱导 MCF-7 细胞在 G0/G1 期停滞,对 HMEC 正常对照细胞没有不良的细胞周期停滞作用。综上所述,从马来西亚热带姜中分离出的 AEA 代表了一种潜在的化疗药物,可用于治疗人类乳腺癌细胞,其细胞毒性效力高于类似物 ACA。

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