Suppr超能文献

miRNA-205 是肾细胞癌中靶向 ZEB2 的候选肿瘤抑制因子。

miRNA-205 is a candidate tumor suppressor that targets ZEB2 in renal cell carcinoma.

机构信息

Department of Urology, Xiangya Hospital, Central South University, Changsha, China.

出版信息

Oncol Res Treat. 2014;37(11):658-64. doi: 10.1159/000368792. Epub 2014 Oct 17.

Abstract

BACKGROUND

This study aims to characterize the function of downregulated MicroRNA miR-205 in renal cell carcinoma (RCC), and show how the downstream zinc finger E-box-binding homeobox 2 (ZEB2) is negatively regulated by miR-205.

MATERIALS AND METHODS

The expression of miR-205 was detected in RCC and adjacent non-tumor tissues using real-time polymerase chain reaction (PCR). The expression of miR-205 and ZEB2 was detected in RCC cell lines using real-time PCR. The luciferase reporter assay was used to assess ZEB2 as a target of miR-205. Protein levels of ZEB2, E-cadherin, and vimentin were measured by western blot after overexpression of miR-205 in ACHN cells. In vivo functions of miR-205 in ACHN cells were measured by MTT assays, migration and invasion assays, and flow cytometry.

RESULTS

MiR-205 was significantly downregulated in RCC samples and cell lines compared with matched non-tumor tissues and HK-2 cells, respectively. No significant difference was found in miR-205 expression between well differentiated and poorly to moderately differentiated groups or between phase I and phase II-III. ZEB2 was upregulated in RCC cell lines compared with expression in HK-2 cells. Upregulation of miR-205 expression caused the downregulation of ZEB2 and vimentin, and the upregulation of E-cadherin in ACHN cells. miR-205 also inhibited proliferation, migration, and invasion, and induced apoptosis of ACHN cells.

CONCLUSION

miR-205 is a candidate tumor suppressor that targets ZEB2 in RCC.

摘要

背景

本研究旨在探讨下调的 MicroRNA miR-205 在肾细胞癌(RCC)中的作用,并展示下游锌指 E 盒结合同源盒 2(ZEB2)如何受 miR-205 负调控。

材料与方法

采用实时聚合酶链反应(PCR)检测 RCC 及相邻非肿瘤组织中 miR-205 的表达。采用实时 PCR 检测 RCC 细胞系中 miR-205 和 ZEB2 的表达。采用荧光素酶报告基因实验评估 ZEB2 是否为 miR-205 的靶标。在 ACHN 细胞中转染 miR-205 后,通过 Western blot 检测 ZEB2、E-钙黏蛋白和波形蛋白的蛋白水平。通过 MTT 测定、迁移和侵袭测定以及流式细胞术检测 miR-205 在 ACHN 细胞中的体内功能。

结果

与匹配的非肿瘤组织和 HK-2 细胞相比,miR-205 在 RCC 样本和细胞系中的表达明显下调。miR-205 的表达在高分化和低-中分化组或 I 期和 II-III 期之间无显著差异。与 HK-2 细胞相比,ZEB2 在 RCC 细胞系中上调。上调 miR-205 的表达导致 ZEB2 和波形蛋白下调,以及 E-钙黏蛋白在 ACHN 细胞中上调。miR-205 还抑制 ACHN 细胞的增殖、迁移和侵袭,并诱导其凋亡。

结论

miR-205 是 RCC 中靶向 ZEB2 的候选肿瘤抑制因子。

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