首页> 外文期刊>International Journal of Molecular Sciences >Involvement of miR-20a in Promoting Gastric Cancer Progression by Targeting Early Growth Response 2 (EGR2)
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Involvement of miR-20a in Promoting Gastric Cancer Progression by Targeting Early Growth Response 2 (EGR2)

机译:miR-20a通过靶向早期生长反应2(EGR2)参与促进胃癌的进展。

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Gastric cancer (GC) is one of the most common cancers, with high incidences in East Asia. microRNAs (miRNAs) play essential roles in the carcinogenesis of GC. miR-20a was elevated in GC, while the potential function of miR-20a was poorly understood. miR-20a expression was examined in GC tissues and cell lines. The effects of miR-20a on the growth, migration, invasion, and chemoresistance of GC cells were examined. Luciferase reporter assay and Western blot were used to screen the target of miR-20a. miR-20a was increased in GC tissues and cell lines. miR-20a promoted the growth, migration and invasion of GC cells, enhanced the chemoresistance of GC cells to cisplatin and docetaxel. Luciferase activity and Western blot confirmed that miR-20a negatively regulated EGR2 expression. Overexpression of EGR2 significantly attenuated the oncogenic effect of miR-20a. miR-20a was involved in the carcinogenesis of GC through modulation of the EGR2 signaling pathway.
机译:胃癌(GC)是最常见的癌症之一,在东亚地区发病率很高。 microRNA(miRNA)在GC的癌变过程中起重要作用。 GC中miR-20a升高,而人们对miR-20a的潜在功能知之甚少。在GC组织和细胞系中检查了miR-20a的表达。检查了miR-20a对GC细胞生长,迁移,侵袭和化学抗性的影响。萤光素酶报告基因测定和蛋白质印迹用于筛选miR-20a的靶标。在GC组织和细胞系中miR-20a升高。 miR-20a促进了GC细胞的生长,迁移和侵袭,增强了GC细胞对顺铂和多西他赛的化学耐药性。荧光素酶活性和蛋白质印迹证实miR-20a负调节EGR2表达。 EGR2的过表达显着减弱了miR-20a的致癌作用。 miR-20a通过调节EGR2信号通路参与了GC的癌变。

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