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人参二醇和表没食子儿茶素没食子酸酯在人结直肠癌细胞中的协同凋亡相互作用。

The synergistic apoptotic interaction of panaxadiol and epigallocatechin gallate in human colorectal cancer cells.

机构信息

Tang Center for Herbal Medicine Research, University of Chicago, Chicago, IL 60637, USA.

出版信息

Phytother Res. 2013 Feb;27(2):272-7. doi: 10.1002/ptr.4707. Epub 2012 May 8.

Abstract

Panaxadiol (PD) is a purified sapogenin of ginseng saponins, which exhibits anticancer activity. Epigallocatechin gallate (EGCG), a major catechin in green tea, is a strong botanical antioxidant. In this study, we investigated the possible synergistic anticancer effects of PD and EGCG on human colorectal cancer cells and explored the potential role of apoptosis in the synergistic activities. Effects of selected compounds on HCT-116 and SW-480 human colorectal cancer cells were evaluated by a modified trichrome stain cell proliferation analysis. Cell cycle distribution and apoptotic effects were analyzed by flow cytometry after staining with PI/RNase or annexin V/PI. Cell growth was suppressed after treatment with PD (10 and 20 µm) for 48 h. When PD (10 and 20 µm) was combined with EGCG (10, 20, and 30 µm), significantly enhanced antiproliferative effects were observed in both cell lines. Combining 20 µm of PD with 20 and 30 µm of EGCG significantly decreased S-phase fractions of cells. In the apoptotic assay, the combination of PD and EGCG significantly increased the percentage of apoptotic cells compared with PD alone (p < 0.01). The synergistic apoptotic effects were also supported by docking analysis, which demonstrated that PD and EGCG bound in two different sites of the annexin V protein. Data from this study suggested that apoptosis might play an important role in the EGCG-enhanced antiproliferative effects of PD on human colorectal cancer cells.

摘要

人参二醇(PD)是人参皂甙的一种纯化皂素,具有抗癌活性。表没食子儿茶素没食子酸酯(EGCG)是绿茶中的一种主要儿茶素,是一种很强的植物抗氧化剂。在这项研究中,我们研究了 PD 和 EGCG 对人结肠癌细胞的协同抗癌作用,并探讨了细胞凋亡在协同作用中的潜在作用。通过改良三色染色细胞增殖分析评估选定化合物对 HCT-116 和 SW-480 人结肠癌细胞的影响。用 PI/RNase 或 Annexin V/PI 染色后,通过流式细胞术分析细胞周期分布和凋亡效应。用 PD(10 和 20μm)处理 48h 后,细胞生长受到抑制。当 PD(10 和 20μm)与 EGCG(10、20 和 30μm)联合使用时,在两种细胞系中均观察到明显增强的抗增殖作用。用 20μm PD 与 20 和 30μm EGCG 联合使用时,细胞 S 期分数明显降低。在凋亡试验中,与 PD 单独作用相比,PD 和 EGCG 的联合作用显著增加了凋亡细胞的百分比(p<0.01)。结合分析也表明 PD 和 EGCG 结合在 annexin V 蛋白的两个不同部位,支持了协同凋亡作用。这项研究的数据表明,细胞凋亡可能在 EGCG 增强 PD 对人结肠癌细胞的抗增殖作用中起重要作用。

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