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miR-448 通过下调 CTTN 抑制脑胶质瘤细胞增殖并促进其凋亡

MiR-448 downregulates CTTN to inhibit cell proliferation and promote apoptosis in glioma.

机构信息

Department of Neurological Surgery, Peking University Ninth School of Clinical Medicine, Beijing, China.

出版信息

Eur Rev Med Pharmacol Sci. 2018 Jun;22(12):3847-3854. doi: 10.26355/eurrev_201806_15269.

Abstract

OBJECTIVE

miRNAs have been confirmed to be related to cell proliferation and apoptosis. In this study, we detected the potential effect of miR-448 on glioma cell proliferation and apoptosis.

MATERIALS AND METHODS

miR-448 and CTTN expression levels were detected in glioma cell lines with quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR). Cells were transfected with miR-448 mimics and inhibitor by using lipofectamine 2000 respectively. The proliferative ability of transfected cells was detected via methyl thiazolyl tetrazolium (MTT) and cell counting kit-8 (CCK8) assays. Cell apoptosis and cell-cycle were tested using flow cytometry. The regulatory correlation between miR-448 and CTTN was explored by bioinformatics analysis and luciferase reporter assay.

RESULTS

Lower expression of miR-448 and higher level of CTTN were detected in glioma cells. MiR-448 could regulate cell proliferation, cell apoptosis, and cell cycle. CTTN was negatively regulated by miR-448.

CONCLUSIONS

miR-448 downregulates CTTN to inhibit cell proliferation and promote apoptosis in glioma, which indicates a potential therapeutic target of glioma.

摘要

目的

miRNA 已被证实与细胞增殖和凋亡有关。本研究旨在检测 miR-448 对神经胶质瘤细胞增殖和凋亡的潜在影响。

材料与方法

采用实时定量逆转录聚合酶链反应(qRT-PCR)检测神经胶质瘤细胞系中 miR-448 和 CTTN 的表达水平。分别用脂质体 2000 将 miR-448 模拟物和抑制剂转染细胞。通过甲基噻唑基四唑(MTT)和细胞计数试剂盒-8(CCK8)检测转染细胞的增殖能力。采用流式细胞术检测细胞凋亡和细胞周期。通过生物信息学分析和荧光素酶报告基因检测探索 miR-448 和 CTTN 之间的调控关系。

结果

神经胶质瘤细胞中 miR-448 表达降低,CTTN 水平升高。miR-448 可调节细胞增殖、细胞凋亡和细胞周期。CTTN 受 miR-448 负调控。

结论

miR-448 通过下调 CTTN 抑制神经胶质瘤细胞增殖并促进其凋亡,提示其可能成为神经胶质瘤的潜在治疗靶点。

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