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绿茶多酚表没食子儿茶素没食子酸酯通过上调miR-1抑制骨肉瘤细胞生长。

Green tea polyphenol EGCG suppresses osteosarcoma cell growth through upregulating miR-1.

作者信息

Zhu Kewei, Wang Wanchun

机构信息

Department of Orthopedics, The 2nd Xiangya Hospital of Central South University, 139 Middle Renmin Road, Changsha, 410011, China.

出版信息

Tumour Biol. 2016 Apr;37(4):4373-82. doi: 10.1007/s13277-015-4187-3. Epub 2015 Oct 24.

Abstract

(-)-Epigallocatechin-3-gallate (EGCG), the most abundant and active polyphenol in green tea, has been demonstrated to have anticancer effects in a wide variety of human cancer. MicroRNAs (miRNAs) are a class of short noncoding RNAs and play important role in gene regulation and are critically involved in the pathogenesis and progression of human cancer. This study aims to investigate the effects of EGCG on osteosarcoma (OS) cells and elucidate the underlying mechanism. Cellular function assays revealed that EGCG inhibited cell proliferation, induced cell cycle arrest and promoted apoptosis of OS cells in vitro, and also inhibited the growth of transplanted tumors in vivo. By miRNA microarray and RT-qPCR analysis, miR-1 was found to be significantly upregulated in MG-63 and U-2OS treated by EGCG in dose- and time-dependent manners, and miR-1 downregulation by inhibitor mimics attenuated EGCG-induced inhibition on cell growth of OS cells. We also confirmed that miR-1 was also frequently decreased in clinical OS tumor tissues. Moreover, both EGCG and miR-1 mimic inhibited c-MET expression, and combination treatment with EGCG and c-MET inhibitor (crizotinib) had enhanced inhibitory effects on the growth of MG-63 and U-2OS cells. Taken together, these results suggest that EGCG has an anticancer effect on OS cells, at least partially, through regulating miR-1/c-MET interaction.

摘要

(-)-表没食子儿茶素-3-没食子酸酯(EGCG)是绿茶中含量最丰富且活性最强的多酚类物质,已被证明在多种人类癌症中具有抗癌作用。微小RNA(miRNA)是一类短链非编码RNA,在基因调控中发挥重要作用,并且在人类癌症的发病机制和进展中起着关键作用。本研究旨在探讨EGCG对骨肉瘤(OS)细胞的影响,并阐明其潜在机制。细胞功能测定表明,EGCG在体外抑制OS细胞的增殖,诱导细胞周期停滞并促进其凋亡,在体内也抑制移植瘤的生长。通过miRNA微阵列和RT-qPCR分析发现,在经EGCG处理的MG-63和U-2OS细胞中,miR-1以剂量和时间依赖性方式显著上调,用抑制剂模拟物下调miR-1可减弱EGCG诱导的对OS细胞生长的抑制作用。我们还证实,在临床OS肿瘤组织中miR-1也经常降低。此外,EGCG和miR-1模拟物均抑制c-MET表达,EGCG与c-MET抑制剂(克唑替尼)联合治疗对MG-63和U-2OS细胞的生长具有增强的抑制作用。综上所述,这些结果表明EGCG至少部分地通过调节miR- /c-MET相互作用对OS细胞具有抗癌作用。 1

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