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微小RNA-182在骨肉瘤细胞中的表达及调控作用:一项初步研究。

Expression and regulatory effects of microRNA-182 in osteosarcoma cells: A pilot study.

作者信息

Bian Dong-Lin, Wang Xue-Mei, Huang Kun, Zhai Qi-Xi, Yu Gui-Bo, Wu Cheng-Hua

机构信息

Department of Ultrasound, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning 110001, P.R. China.

Key Laboratory of Diagnosis and Interventional Therapy of Liaoning Province, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning 110001, P.R. China.

出版信息

Oncol Lett. 2016 May;11(5):3040-3048. doi: 10.3892/ol.2016.4375. Epub 2016 Mar 23.

Abstract

The aim of the present study was to evaluate the expression level of microRNA-182 (miRNA-182) in human osteosarcoma (OS) MG-63 cells and OS tissues, and to elucidate the effect of miRNA-182 on the biological activity of tumors. In the present study, the expression of miRNA-182 in human OS MG-63 cells, OS tissues and normal osteoblast hFOB1.19 cells was determined using quantitative polymerase chain reaction. Subsequently, a miRNA-182 mimic and inhibitor were utilized to regulate the expression level of this miRNA in MG-63 cells. Cell viability and proliferation were examined using cell counting kit-8 assays, and cell apoptosis was detected by flow cytometry. Cell invasion and migration assays were performed using Transwell chambers to analyze the biological functions of miRNA-182 . The present study demonstrated that the expression level of miRNA-182 in MG-63 cells and OS tissues was significantly increased compared with the hFOB1.19 cell line (P<0.05). The present study successfully performed cell transfections of miRNA-182 inhibitor and miRNA-182 mimic into MG-63 cells and achieved the desired transfection efficiency. The present study confirmed that upregulation of miRNA-182 promotes cell apoptosis and inhibits cell viability, proliferation, invasion and migration. The present findings additionally demonstrated that miRNA-182 is a tumor suppressor gene in OS. Therefore, regulating the expression of miRNA-182 may affect the biological behavior of OS cells, which suggests a potential role for miRNA-182 in molecular therapy for malignant tumors.

摘要

本研究的目的是评估微小RNA-182(miRNA-182)在人骨肉瘤(OS)MG-63细胞和OS组织中的表达水平,并阐明miRNA-182对肿瘤生物学活性的影响。在本研究中,采用定量聚合酶链反应测定miRNA-182在人OS MG-63细胞、OS组织和正常成骨细胞hFOB1.19细胞中的表达。随后,利用miRNA-182模拟物和抑制剂来调节MG-63细胞中该miRNA的表达水平。使用细胞计数试剂盒-8检测法检测细胞活力和增殖情况,并通过流式细胞术检测细胞凋亡。使用Transwell小室进行细胞侵袭和迁移试验,以分析miRNA-182的生物学功能。本研究表明,与hFOB1.19细胞系相比,MG-63细胞和OS组织中miRNA-182的表达水平显著升高(P<0.05)。本研究成功地将miRNA-182抑制剂和miRNA-182模拟物转染到MG-63细胞中,并达到了预期的转染效率。本研究证实,miRNA-182的上调促进细胞凋亡,并抑制细胞活力、增殖、侵袭和迁移。本研究结果还表明,miRNA-182是OS中的一种肿瘤抑制基因。因此,调节miRNA-182的表达可能会影响OS细胞的生物学行为,这表明miRNA-182在恶性肿瘤的分子治疗中具有潜在作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fd0/4840939/ea34524e66bc/ol-11-05-3040-g00.jpg

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