Suppr超能文献

(-)-表没食子儿茶素-3-没食子酸酯与EZH2抑制剂GSK343对结肠癌细胞具有相似的抑制作用和作用机制。

(-)-Epigallocatechin-3-gallate and EZH2 inhibitor GSK343 have similar inhibitory effects and mechanisms of action on colorectal cancer cells.

作者信息

Ying Le, Yan Feng, Williams Bryan Rg, Xu Ping, Li Xin, Zhao Yueling, Hu Yiqun, Wang Yuefei, Xu Dakang, Dai Jing

机构信息

Department of Tea Science, Zhejiang University, Hangzhou, China.

Hudson Institute of Medical Research, Clayton, Victoria, Australia.

出版信息

Clin Exp Pharmacol Physiol. 2018 Jan;45(1):58-67. doi: 10.1111/1440-1681.12854. Epub 2017 Nov 2.

Abstract

Epigallocatechin-3-gallate (EGCG) is a type of catechin. It exhibits excellent antioxidant effects and anti-tumour activities for cancer chemoprevention. The mechanism of anti-tumour effects of EGCG on different cancers has been studied for the past few decades, but remains controversial. To investigate the potential role that EGCG may play in the epigenetic regulation of colorectal cancer (CRC) cell line, we integrated bioinformatics analysis with experimental validation. We found that levels of the enhancer of zeste homologue 2 (EZH2) were significantly higher in CRC tissues compared to normal adjacent tissues, based on the Genomic Data Commons (GDC) data portal. Different human CRC cell lines exhibited differing expression of levels of the EZH2 protein. In RKO cells, EGCG and the EZH2 inhibitor GSK343 exhibited similar inhibitory efficacy on the proliferation, invasion and migration abilities of the cells, and suppressed protein expression of trimethylated lysine 27 on histone H3 (H3K27me3), which may be caused by the loss of the enzymatic function of EZH2. EGCG and GSK343 were found to have a synergistic effect on the growth of RKO cells in lower concentrations. EZH2-correlated genes were enriched in the cell cycle pathway, the top-ranking up-regulated pathway in tumour tissues, based on pathway analyses using the Kyoto Encyclopedia of Genes and Genomes (KEGG) and Gene Set Enrichment Analysis (GSEA). In accord with this, we confirmed that EGCG and GSK343 could both significantly arrest the G0/G1 phase in RKO cell cycle, suggesting EGCG and EZH2 inhibitor share a common mechanism of action in RKO cells.

摘要

表没食子儿茶素-3-没食子酸酯(EGCG)是一种儿茶素。它具有出色的抗氧化作用和抗肿瘤活性,可用于癌症化学预防。在过去几十年中,人们对EGCG对不同癌症的抗肿瘤作用机制进行了研究,但仍存在争议。为了研究EGCG在结直肠癌(CRC)细胞系表观遗传调控中可能发挥的潜在作用,我们将生物信息学分析与实验验证相结合。基于基因组数据共享库(GDC)数据门户,我们发现与相邻正常组织相比,CRC组织中zeste同源物2(EZH2)增强子的水平显著更高。不同的人CRC细胞系EZH2蛋白表达水平不同。在RKO细胞中,EGCG和EZH2抑制剂GSK343对细胞的增殖、侵袭和迁移能力表现出相似的抑制效果,并抑制组蛋白H3赖氨酸27三甲基化(H3K27me3)的蛋白表达,这可能是由于EZH2酶功能丧失所致。发现EGCG和GSK343在较低浓度下对RKO细胞生长具有协同作用。基于使用京都基因与基因组百科全书(KEGG)和基因集富集分析(GSEA)的通路分析,EZH2相关基因在细胞周期通路中富集,这是肿瘤组织中上调排名最高的通路。与此一致的是,我们证实EGCG和GSK343均可显著使RKO细胞周期停滞于G0/G1期,表明EGCG和EZH2抑制剂在RKO细胞中具有共同的作用机制。

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