Department of Vascular Intervention, Jingmen No.2 People's Hospital, Jingmen, China.
Department of Interventional Medicine, Zaozhuang Municipal Hospital, Zaozhuang, China.
Cancer Biother Radiopharm. 2021 Dec;36(10):850-862. doi: 10.1089/cbr.2019.3297. Epub 2020 Jun 24.
The current study aimed to investigate the effects of on the migration and invasion of hepatoma cells. The expressions of , miR-137, and were detected in hepatoma tissues and cells by performing quantitative reverse transcription-polymerase chain reaction (qRT-PCR). The correlations among , miR-137, and were predicted by bioinformatics analysis and confirmed by dual-luciferase reporter assay, and Pearson test was performed to analyze their relevance. The effects of , miR-137, and on viability, migration, and invasion of transfected hepatoma cells were detected by CCK-8, wound scratch, and Transwell. Epithelial-mesenchymal transition (EMT)-related protein levels were determined by Western blot and qRT-PCR. was highly expressed in hepatoma tissues and cells. Silencing expression inhibited the viability, migration, and invasion of hepatoma cells. targeted miR-137 and the two was negatively correlated, and silencing TUG1 expression inhibited the effects of low-expressed miR-137 on promoting proliferation, migration, and invasion of hepatoma cells. was predicted to be the target gene for miR-137, and the two were negatively correlated. Moreover, inhibiting miR-137 expression promoted the expression of , , and N-cadherin and inhibited E-cadherin expression, while silencing expression reversed the effects of low-expressed miR-137 on EMT-related protein levels. LncRNA promotes hepatocellular carcinoma migration and invasion through targeting the miR-137/AKT2 axis.
本研究旨在探讨 LncRNA 对肝癌细胞迁移和侵袭的影响。通过定量逆转录-聚合酶链反应(qRT-PCR)检测肝癌组织和细胞中、miR-137 和的表达。通过生物信息学分析预测和双荧光素酶报告基因实验验证,分析之间的相关性,并通过 Pearson 检验分析它们的相关性。通过 CCK-8、划痕实验和 Transwell 检测转染肝癌细胞活力、迁移和侵袭的影响。通过 Western blot 和 qRT-PCR 检测上皮间质转化(EMT)相关蛋白水平。结果显示,在肝癌组织和细胞中表达较高。沉默表达抑制肝癌细胞的活力、迁移和侵袭。靶向 miR-137,二者呈负相关,沉默 TUG1 表达抑制低表达 miR-137 对促进肝癌细胞增殖、迁移和侵袭的作用。预测为 miR-137 的靶基因,二者呈负相关。此外,抑制 miR-137 表达促进、、N-钙黏蛋白的表达,抑制 E-钙黏蛋白的表达,而沉默表达逆转低表达 miR-137 对 EMT 相关蛋白水平的影响。LncRNA 通过靶向 miR-137/AKT2 轴促进肝癌细胞迁移和侵袭。