Lu Qingfu, Guo Zhaoji, Qian Haixin
Department of General Surgery, The First Affiliated Hospital of Soochow University, Suzhou, Jiangsu 215006, P.R. China.
Exp Ther Med. 2019 Mar;17(3):2221-2229. doi: 10.3892/etm.2019.7206. Epub 2019 Jan 28.
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.
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。