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微小RNA-150-5p/SRCIN1轴在乳腺癌进展中的作用。

Role of microRNA-150-5p/SRCIN1 axis in the progression of breast cancer.

作者信息

Lu Qingfu, Guo Zhaoji, Qian Haixin

机构信息

Department of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, P.R. China.

出版信息

Exp Ther Med. 2019 Mar;17(3):2221-2229. doi: 10.3892/etm.2019.7206. Epub 2019 Jan 28.

Abstract

In China, breast cancer is the most commonly occurring cancer in women. MicroRNAs (miRs) are a group of endogenous small non-coding RNAs, which serve a role in many biological processes through the regulation of target genes. In the current study, miR-150-5p expression was significantly up-regulated in breast cancer tissues and cell lines. To investigate the cellular function and underlying molecular mechanism of miR-150-5p in breast cancer, TargetScan7.2 was used to identify miR-150-5p target genes. SRC kinase signaling inhibitor 1 (SRCIN1) was identified as a direct target gene of miR-150-5p and the current study demonstrated that SRCIN1 was negatively regulated by miR-150-5p in breast cancer cells. Furthermore, SRCIN1 expression was significantly down-regulated in breast cancer tissues and cell lines. Taken together, these results demonstrated that there was a negative association between miR-150-5p and SRCIN1 in breast cancer. The CCK-8 and Transwell assays were used to examine breast cancer cell viability, invasion and migration ability. The current study demonstrated that over-expression of miR-150-5p enhanced breast cancer cell proliferation, invasion and migration. In addition, miR-150-5p over-expression increased the expression of mesenchymal cell markers (vimentin, N-cadherin and β-catenin) and decreased the expression of epithelial cell markers (E-cadherin and zonula occludens-1). By contrast, miR-150-5p knockdown inhibited breast cancer cell viability, invasion and migration. Additionally, miR-150-5p knockdown decreased the expression of mesenchymal cell markers and increased the expression of epithelial cell markers. Taken together, these results suggest that the miR-150-5p/SRCIN1 axis may be a potential target in the treatment of breast cancer.

摘要

在中国,乳腺癌是女性中最常见的癌症。微小RNA(miR)是一类内源性小非编码RNA,通过调控靶基因在许多生物学过程中发挥作用。在本研究中,miR-150-5p在乳腺癌组织和细胞系中表达显著上调。为了研究miR-150-5p在乳腺癌中的细胞功能和潜在分子机制,使用TargetScan7.2来鉴定miR-150-5p的靶基因。SRC激酶信号抑制剂1(SRCIN1)被鉴定为miR-150-5p的直接靶基因,本研究表明在乳腺癌细胞中SRCIN1受到miR-150-5p的负调控。此外,SRCIN1在乳腺癌组织和细胞系中的表达显著下调。综上所述,这些结果表明在乳腺癌中miR-150-5p与SRCIN1之间存在负相关。使用CCK-8和Transwell实验检测乳腺癌细胞的活力、侵袭和迁移能力。本研究表明miR-150-5p的过表达增强了乳腺癌细胞的增殖、侵袭和迁移。此外,miR-150-5p的过表达增加了间充质细胞标志物(波形蛋白、N-钙黏蛋白和β-连环蛋白)的表达,并降低了上皮细胞标志物(E-钙黏蛋白和闭合蛋白-1)的表达。相反,miR-150-5p的敲低抑制了乳腺癌细胞的活力、侵袭和迁移。此外,miR-150-5p的敲低降低了间充质细胞标志物的表达,并增加了上皮细胞标志物的表达。综上所述,这些结果表明miR-150-5p/SRCIN1轴可能是乳腺癌治疗的一个潜在靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f286/6396020/870e9cfbdf9c/etm-17-03-2221-g00.jpg

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