Suppr超能文献

儿茶素水合物通过 TP53/Caspase 介导的细胞凋亡抑制 MCF-7 增殖。

Catechin hydrate suppresses MCF-7 proliferation through TP53/Caspase-mediated apoptosis.

机构信息

Molecular Cancer Biology Research Lab, Dept, of Food Science and Nutrition, College of Agriculture and Food Sciences, King Saud University, Saudi Arabia.

出版信息

J Exp Clin Cancer Res. 2010 Dec 17;29(1):167. doi: 10.1186/1756-9966-29-167.

Abstract

Catechin hydrate (CH), a strong antioxidant that scavenges radicals, is a phenolic compound that is extracted from plants and is present in natural food and drinks, such as green tea and red wine. CH possesses anticancer potential. The mechanism of action of many anticancer drugs is based on their ability to induce apoptosis. In this study, I sought to characterize the downstream apoptotic genes targeted by CH in MCF-7 human breast cancer cells. CH effectively kills MCF-7 cells through induction of apoptosis. Apoptosis was confirmed by terminal deoxynucleotidyl transferase-mediated dUTP nick end labeling (TUNEL) and real-time PCR assays. Cells were exposed to 150 μg/ml CH and 300 μg/mL CH for 24 hours, which resulted in 40.7% and 41.16% apoptotic cells, respectively. Moreover, a 48-hour exposure to 150 μg/ml CH and 300 μg/ml CH resulted in 43.73% and 52.95% apoptotic cells, respectively. Interestingly, after 72 hours of exposure to both concentrations of CH, almost 100% of cells lost their integrity. These results were further confirmed by the increased expression of caspase-3,-8, and -9 and TP53 in a time-dependent and dose-dependent manner, as determined by real-time quantitative PCR. In summary, the induction of apoptosis by CH is affected by its ability to increase the expression of pro-apoptotic genes such as caspase-3, -8, and -9 and TP53.

摘要

儿茶素水合物(CH)是一种从植物中提取的具有抗氧化活性的酚类化合物,可清除自由基,存在于绿茶和红酒等天然食品和饮料中。CH 具有抗癌潜力。许多抗癌药物的作用机制基于其诱导细胞凋亡的能力。在这项研究中,我试图描述 CH 在 MCF-7 人乳腺癌细胞中靶向的下游凋亡基因。CH 通过诱导细胞凋亡有效地杀死 MCF-7 细胞。通过末端脱氧核苷酸转移酶介导的 dUTP 缺口末端标记(TUNEL)和实时 PCR 分析证实了细胞凋亡。将细胞暴露于 150μg/ml CH 和 300μg/ml CH 24 小时,分别导致 40.7%和 41.16%的凋亡细胞。此外,暴露于 150μg/ml CH 和 300μg/ml CH 48 小时分别导致 43.73%和 52.95%的凋亡细胞。有趣的是,在暴露于两种浓度的 CH72 小时后,几乎 100%的细胞失去完整性。通过实时定量 PCR 还以时间和剂量依赖的方式确定 caspase-3、-8 和 -9 以及 TP53 的表达增加进一步证实了这一点。总之,CH 通过增加促凋亡基因如 caspase-3、-8 和 -9 以及 TP53 的表达诱导细胞凋亡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fd7/3019143/85b73ea23092/1756-9966-29-167-1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验