蛋白葡聚糖与维生素K3联合对膀胱癌细胞的抗癌作用

Michael Zhang, Kelvin Zheng, M. Choudhury, J. Phillips, S. Konno
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引用次数: 2

摘要

目的:蘑菇提取物(PDF)是一种具有抗癌/抗肿瘤活性的生物活性蛋白葡聚糖,维生素K3 (VK3)是人工合成的具有抗肿瘤活性的VK衍生物。一种使用这两种药物的非常规方法在体外测试了它们对膀胱癌细胞的抗癌作用。方法:采用PDF、VK3或两者联合处理膀胱癌T24细胞,采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑法测定细胞活力。为了探讨其抗癌机制,我们专门研究了细胞周期和表观遗传改变。结果:PDF≥500 μg/mL可使细胞活力降低35%,而VK3对细胞活力无明显影响。而当PDF (300 μg/mL)与VK3 (5 μM)联合作用时,细胞活力降低75%。这种特异性组合诱导G1细胞周期阻滞,并下调G1特异性调节因子。组蛋白去乙酰化酶失活,组蛋白3和4高度乙酰化。两种凋亡调节因子也被PDF/VK3联合显著激活。结论:PDF与VK3特异性联用可增强T24细胞的抗癌作用。这主要归因于G1细胞周期阻滞和染色质修饰,最终导致细胞凋亡。因此,PDF/VK3联合治疗可能为膀胱癌提供一种潜在的治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Enhanced anticancer effect by combination of proteoglucan and Vitamin K3 on bladder cancer cells
Aim: Mushroom extract, PDF, is a bioactive proteoglucan with anticancer/antitumor activity, and Vitamin K3 (VK3) is a synthetic VK derivative with antitumor activity as well. An unconventional approach using these two agents was tested to see their anticancer effects on bladder cancer cells in vitro. Methods: Human bladder cancer T24 cells were treated with PDF, VK3, or their combination, and cell viability was assessed by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-tetrazolium bromide assay. To explore the anticancer mechanism, cell cycle and epigenetic alterations were specifically studied. Results: PDF ≥ 500 μg/mL led to a ~ 35% reduction in cell viability while VK3 had little effects. However, when PDF (300 μg/mL) was combined with VK3 (5 μM), a ~ 75% cell viability reduction was attained. This specific combination induced a G1 cell cycle arrest with the downregulation of G1-specific regulators. In addition, histone deacetylase was inactivated while histones 3 and 4 were highly acetylated. Two apoptotic regulators were significantly activated with PDF/VK3 combination as well. Conclusion: The specific combination of PDF and VK3 appears to potentiate anticancer effect on T24 cells. This is primarily attributed to a G1 cell cycle arrest with chromatin modifications, ultimately leading to apoptosis. Thus, the PDF/VK3 combination may offer a potential therapeutic option for bladder cancer.
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