功能茶提取物抑制细胞生长、诱导细胞凋亡并导致人类肝细胞癌细胞系 G0/G1 停滞,可能是通过降低端粒酶活性实现的

Foods Pub Date : 2024-06-14 DOI:10.3390/foods13121867
Yuan Chen, Changsong Chen, Jiaxin Xiang, Ruizhen Gao, Guojun Wang, Wenquan Yu
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引用次数: 0

摘要

根据 "健康中国 "国家项目,功能茶 CFT-1 已作为营养保健饮料引入中国。功能茶提取物(纯度大于 98%)对人类肝细胞癌(HCC)细胞的影响尚不明确。用显微镜观察了细胞的形态变化。细胞增殖、迁移、周期分布和凋亡效应分别通过 MTT、Transwell 试验和流式细胞术进行评估,端粒酶抑制作用则通过端粒酶 PCR ELISA 检测试剂盒进行评估。经 CFT-1 处理的细胞出现萎缩、核焦缩和染色质凝集。CFT-1通过诱导Hep3B细胞凋亡和G0/G1停滞,抑制了Hep3B细胞的生长,IC50为143 μg/mL。在分子机制方面,CFT-1能有效降低端粒酶活性。功能茶提取物通过诱导细胞凋亡和G0/G1停滞来抑制人类HCC细胞的生长,这可能是通过降低端粒酶活性实现的。这些结果表明,CFT-1提取物具有体外抗癌活性,为今后开发和利用CFT-1作为功能食品来抑制HCC细胞增殖提供了启示。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional Tea Extract Inhibits Cell Growth, Induces Apoptosis, and Causes G0/G1 Arrest in Human Hepatocellular Carcinoma Cell Line Possibly through Reduction in Telomerase Activity
The functional tea CFT-1 has been introduced into China as a nutraceutical beverage according to the “Healthy China” national project. The effects on human hepatocellular carcinoma (HCC) cells remain unclear and were investigated with the functional tea extract (purity > 98%). The morphological changes in the cells were observed with microscopes. Cell proliferation, migration, cycle distribution, and apoptotic effects were assessed by MTT, Transwell assays, and flow cytometry, respectively, while telomerase inhibition was evaluated with telomerase PCR ELISA assay kits. The CFT-1 treatment resulted in cell shrinkage, nuclear pyknosis, and chromatin condensation. CFT-1 suppressed the growth of Hep3B cells with IC50 of 143 μg/mL by inducing apoptosis and G0/G1 arrest in Hep3B cells. As for the molecular mechanism, CFT-1 treatment can effectively reduce the telomerase activity. The functional tea extract inhibits cell growth in human HCC by inducing apoptosis and G0/G1 arrest, possibly through a reduction in telomerase activity. These results indicate that CFT-1 extract exhibited in vitro anticancer activities and provided insights into the future development and utilization of CFT-1 as functional foods to inhibit the proliferation of HCC cells.
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