Department of Obstetrics and Gynecology, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China.
Eur Rev Med Pharmacol Sci. 2020 Jun;24(12):6576-6582. doi: 10.26355/eurrev_202006_21642.
The purpose of this study was to investigate the potential effects of miR-613 on the development of cervical squamous cell cancer (CSCC) and the relevant mechanism.
The expression level of miR-613 was detected in CSCC tissues and cells by quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). Thereafter, online prediction software and Luciferase reporter assays were used to evaluate the possible target of miR-613, and the effects of the miR-613 on SiHa cells were determined in vitro. Then, the changes of protein expression in cells were measured by Western blot. Finally, Cell Counting Kit-8 (CCK-8), wound healing and transwell assays were performed to analyze cell proliferation, invasion, and migration.
It was found that compared with that in normal tissues and cells, miR-613 expression was found suppressed in CSCC tissues and cells. Based on bioinformatics and Luciferase results, miR-613 could target and bind to LETM1. Besides, it was found that miR-613 could regulate the expression of LETM1 in SiHa cells, and miR-613 had a valuable suppressive effect on the proliferation, invasion, and migration of SiHa cells through the subsequent experiments. However, when co-transfection of miR-613 mimics and LV-LETM1 into SiHa cells, the anti-cancer effects of miR-613 on SiHa cells vanished.
Taken all, this research discovered the function of miR-613 on CSCC by targeting LETM1, revealing that miR-613/LETM1 signal pathway might be a potential therapeutic target for the diagnosis and treatment of CSCC.
本研究旨在探讨 miR-613 对宫颈鳞状细胞癌(CSCC)发展的潜在影响及其相关机制。
采用实时定量聚合酶链反应(qRT-PCR)检测 CSCC 组织和细胞中 miR-613 的表达水平。然后,利用在线预测软件和荧光素酶报告基因实验评估 miR-613 的可能靶标,并在体外研究 miR-613 对 SiHa 细胞的影响。随后,通过 Western blot 检测细胞中蛋白质表达的变化。最后,通过细胞计数试剂盒-8(CCK-8)、划痕愈合和 Transwell 实验分析细胞增殖、侵袭和迁移。
与正常组织和细胞相比,CSCC 组织和细胞中 miR-613 的表达受到抑制。基于生物信息学和荧光素酶结果,miR-613 可以靶向并结合 LETM1。此外,研究发现 miR-613 可以调节 SiHa 细胞中 LETM1 的表达,并且 miR-613 通过随后的实验对 SiHa 细胞的增殖、侵袭和迁移具有有价值的抑制作用。然而,当 miR-613 模拟物和 LV-LETM1 共转染 SiHa 细胞时,miR-613 对 SiHa 细胞的抗癌作用消失。
综上所述,本研究通过靶向 LETM1 发现了 miR-613 对 CSCC 的作用,表明 miR-613/LETM1 信号通路可能是 CSCC 诊断和治疗的潜在治疗靶点。