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微小RNA-4513通过靶向KAT6B促进胃癌细胞增殖和上皮-间质转化。

MicroRNA-4513 Promotes Gastric Cancer Cell Proliferation and Epithelial-Mesenchymal Transition Through Targeting KAT6B.

作者信息

Ding Huimin, Shi Yuhua, Liu Xiaobing, Qiu Aifeng

机构信息

Department of General Surgery, The First People's Hospital of Yancheng City, Yancheng, P.R. China.

Department of General Surgery, The Third People's Hospital of Yancheng City, Yancheng, P.R. China.

出版信息

Hum Gene Ther Clin Dev. 2019 Sep;30(3):142-148. doi: 10.1089/humc.2019.094.

Abstract

The purpose of this study was to investigate the expression level of microRNA-4513 (miR-4513) in gastric cancer (GC), and to elucidate the mechanisms underlying its regulation of GC progression. Quantitative real-time PCR (qRT-PCR) was performed to measure the expression level of miR-4513 in GC cells. Transfection efficacy of synthetic miRNAs was examined by qRT-PCR. After synthetic miRNA transfection, cell counting kit-8 assay and transwell invasion assay were conducted to measure biological changes in these groups. The key molecular expression level involved in epithelial-mesenchymal transition (EMT) was analyzed by Western blot. Bioinformatic analysis and Western blot were performed to investigate the connection between miR-4513 and lysine acetyltransferase 6B (KAT6B). qRT-PCR results showed that miR-4513 expression level was upregulated in GC cell lines. Downregulation of miR-4513 expression inhibited GC cell proliferation, invasion, and EMT. KAT6B was validated as a direct target of miR-4513. In addition, KAT6B expression level can be upregulated by miR-4513 inhibitor. Collectively, we showed that miR-4513 is involved in regulating the biological function of GC cells via KAT6B. In addition, miR-4513 may serve as a potential target for the molecular therapy of GC.

摘要

本研究旨在探讨微小RNA-4513(miR-4513)在胃癌(GC)中的表达水平,并阐明其调控GC进展的机制。采用定量实时聚合酶链反应(qRT-PCR)检测GC细胞中miR-4513的表达水平。通过qRT-PCR检测合成微小RNA的转染效率。合成微小RNA转染后,采用细胞计数试剂盒-8法和Transwell侵袭试验检测各组的生物学变化。通过蛋白质免疫印迹法分析上皮-间质转化(EMT)相关关键分子的表达水平。采用生物信息学分析和蛋白质免疫印迹法研究miR-4513与赖氨酸乙酰转移酶6B(KAT6B)之间的联系。qRT-PCR结果显示,miR-4513在GC细胞系中的表达水平上调。miR-4513表达下调可抑制GC细胞增殖、侵袭及EMT。KAT6B被证实为miR-4513的直接靶点。此外,miR-4513抑制剂可上调KAT6B的表达水平。综上所述,我们发现miR-4513通过KAT6B参与调控GC细胞的生物学功能。此外,miR-4513可能成为GC分子治疗的潜在靶点。

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