首页> 外文期刊>Journal of Breast Cancer >LncRNA Taurine-Upregulated Gene 1 Promotes Cell Proliferation by Inhibiting MicroRNA-9 in MCF-7 Cells
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LncRNA Taurine-Upregulated Gene 1 Promotes Cell Proliferation by Inhibiting MicroRNA-9 in MCF-7 Cells

机译:LncRNA牛磺酸上调的基因1通过抑制MCF-7细胞中的MicroRNA-9促进细胞增殖。

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Purpose This study was designed to investigate the role of taurine-upregulated gene 1 ( TUG1 ) in MCF-7 breast cancer cells and the molecular mechanism involved in the regulation of microRNA-9 (miR-9). Methods The expression of TUG1 in breast cancer tissues and cells was evaluated using quantitative reverse transcription polymerase chain reaction. Cell viability was examined using a 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) assay; cell cycle progression and apoptosis were analyzed using flow cytometry. A dual luciferase reporter assay was used to detect the relationship between TUG1 and miR-9. The expression of methylenetetrahydrofolate dehydrogenase 2 (MTHFD2) was measured by western blot. Results Higher expression of TUG1 was observed in breast cancer tissues and cell lines than in the corresponding controls. TUG1 knockdown reduced proliferation, suppressed cell cycle progression, and promoted apoptosis of MCF-7 cells. The dual luciferase reporter assay showed that TUG1 could negatively regulate the expression of miR-9. MiR-9 inhibition abrogated the effect of TUG1 knockdown on the proliferation, cell cycle progression, and apoptosis of MCF-7 cells. TUG1 positively regulated the expression of MTHFD2 in breast cancer cells. Conclusion TUG1 knockdown was significantly associated with decreased cell proliferation and it promoted apoptosis of breast cancer cells through the regulation of miR-9.
机译:目的本研究旨在研究牛磺酸上调基因1(TUG1)在MCF-7乳腺癌细胞中的作用,以及参与调控microRNA-9(miR-9)的分子机制。方法采用定量逆转录聚合酶链反应检测TUG1在乳腺癌组织和细胞中的表达。使用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2-H-溴化四唑(MTT)法检测细胞活力;流式细胞仪分析细胞周期进程和凋亡。使用双重荧光素酶报告基因测定法检测TUG1和miR-9之间的关系。通过蛋白质印迹法测定亚甲基四氢叶酸脱氢酶2(MTHFD2)的表达。结果在乳腺癌组织和细胞系中观察到TUG1的表达高于相应的对照。 TUG1组合式减少增殖,抑制细胞周期进程,并促进MCF-7细胞凋亡。双重荧光素酶报告基因检测表明TUG1可以负调控miR-9的表达。 MiR-9抑制消除了TUG1敲低对MCF-7细胞增殖,细胞周期进程和细胞凋亡的影响。 TUG1积极调节MTHFD2在乳腺癌细胞中的表达。结论TUG1敲低与miR-9的表达密切相关,并能促进乳腺癌细胞的凋亡。

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