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首页> 外文期刊>Tropical Journal of Pharmaceutical Research >Effect of miR-384-targeting LINC00491 on proliferation, migration and invasion of tongue squamous cell carcinoma cells
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Effect of miR-384-targeting LINC00491 on proliferation, migration and invasion of tongue squamous cell carcinoma cells

机译:miR-384靶向LINC00491对舌鳞状细胞癌细胞增殖,迁移和侵袭的影响

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Purpose: To investigate the effect of long-chain non-coding RNA LINC00491 (LncRNA LINC00491) on the proliferation, migration and invasion of tongue squamous cell carcinoma (TSCC) cells, and the underlying mechanism. Methods: Real-time quantitative polymerase chain reaction (qRT-PCR) was applied to determine the ex pressions of LINC00491 and micro-RNA-384 (miR-384). Furthermore, LINC00491 and miR-384 were transfected into CAL-27 cells, while cell cycle was analyzed using flow cytometry. Cell proliferation was determined by methyl thiazolyl diphenyl-tetrazolium (MTT) assay. Cell migration and invasion were evaluated using Transwell experiments. The relationship between LINC00491 and miR-384 was confirmed using double luciferase reporting assay, while protein ex pression levels of P21, Ki67, E-cadherin, N-cadherin, and vimentin were assayed with Western blotting. Results: The ex pression of LINC00491 increased in TSCC tissues (p 0.05). The proportion of cells in G1-phase increased, while the proportion of cells in S-phase decreased (p 0.05). There was decrease in cell survival, cell migration and cell invasion (p 0.05). The protein ex pression levels of Ki67, N-cadherin, and vimentin were lowered, while those of P21, E-cadherin protein were increased (p 0.05). Transfection of LINC00491 and miR- 384 reduced the proportion of cells in G1 phase, but increased the proportion of cells in S-phase (p 0.05). Moreover, cell survival, migration and invasion were increased. The protein ex pressions of Ki67, N-cadherin, and vimentin rose, while those of P21 and E-cadherin decreased (p 0.05). Conclusion: LINC00491 promotes the proliferation, migration and invasion of TSCC cells by inhibiting miR-384. This finding provides a potential target for the treatment of TSCC.
机译:目的:探讨长链非编码RNA LINC00491(LNCRNA LINC00491)对舌鳞状细胞癌(TSCC)细胞和潜在机制的增殖,迁移和侵袭的影响。方法:采用实时定量聚合酶链反应(QRT-PCR)确定LINC00491和Micro-RNA-384(miR-384)的Exclim。此外,使用流式细胞术分析细胞周期,将LINC00491和MIR-384转染到CAL-27细胞中。通过甲基噻唑基二苯基 - 四唑(MTT)测定法测定细胞增殖。使用Transwell实验评估细胞迁移和侵袭。使用双荧光素酶报告测定证实了LINC00491和MIR-384之间的关系,而P21,KI67,E-CADERIN,N-CADHERIN和VIMENIN的蛋白质EX压力水平测定。结果:在TSCC组织中增加LINC00491的EX压力(P <0.05)。 G1相中细胞的比例增加,而S相中细胞的比例降低(P <0.05)。细胞存活,细胞迁移和细胞侵袭减少(P <0.05)。降低了Ki67,N-Cadherin和Vimentin的蛋白质EX压力水平,而P21的蛋白质,e-钙粘蛋白蛋白的增加(P <0.05)。 LINC00491和MIR-384的转染减少了G1相中细胞的比例,但在S相中增加了细胞的比例(P <0.05)。此外,细胞存活,迁移和侵袭增加。 Ki67,N-Cadherin和Vimentin的蛋白质Exclum升压,而P21和E-Cadherin的蛋白质降低(P <0.05)。结论:LINC00491通过抑制miR-384促进TSCC细胞的增殖,迁移和侵袭。该发现提供了治疗TSCC的潜在目标。

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