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MicroRNA-140-5p Inhibits the Progression of Colorectal Cancer by Targeting VEGFA

机译:MicroRNA-140-5p通过靶向VEGFA抑制大肠癌的进展

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Background: microRNAs (miRNAs) are small non-coding RNAs and have been shown to play a crucial role in the colorectal cancer (CRC) tumorigenesis and progression. The aim of this study was to investigate the clinical significance and prognostic value of miR-140-5p in CRC. The exact functions and the underlying molecular mechanisms of miR-140-5p in CRC was further determined. Methods: miR-140-5p expression was detected in CRC samples, their adjacent nontumor tissues as well as CRC cell lines by RT-qPCR. Cell proliferation was detected using CCK-8, and cell invasion and migration were evaluated using Transwell assay. The direct regulation of VEGFA by miR-140-5p was identified using luciferase reporter assay. Results: miR-140-5p was significantly dowregulated in CRC tissues and cell lines. Downregulation of miR-140-5p was significantly correlated with advanced CRC stage and poorer overall survival. Both gain-of-function and loss of function studies demonstrated that miR-140-5p acted as a tumor suppressor by inhibiting cell proliferation, migration and invasion. Integrated analysis identified VEGFA as a direct and functional target gene of miR-140-5p. Silencing VEGFA by small interfering RNA (siRNA) resembled the phenotype resulting from ectopic miR-140-5p expression, while overexpression of VEGFA attenuated the effect of miR-140-5p on CRC cells. Conclusions: Our results suggested a tumor suppressive role of miR-140-5p in CRC tumorigenesis and progression by targeting VEGFA.
机译:背景:microRNA(miRNA)是小的非编码RNA,已显示在结直肠癌(CRC)的肿瘤发生和发展中起关键作用。这项研究的目的是调查miR-140-5p在CRC中的临床意义和预后价值。进一步确定了miR-140-5p在CRC中的确切功能和潜在的分子机制。方法:采用RT-qPCR技术检测CRC样本,癌旁组织及癌细胞中miR-140-5p的表达。使用CCK-8检测细胞增殖,并使用Transwell分析评估细胞侵袭和迁移。使用萤光素酶报告基因分析鉴定了miR-140-5p对VEGFA的直接调节。结果:miR-140-5p在CRC组织和细胞系中显着下调。 miR-140-5p的下调与晚期CRC阶段和较差的总生存率显着相关。功能获得和功能丧失研究均证明miR-140-5p通过抑制细胞增殖,迁移和侵袭而充当肿瘤抑制因子。综合分析确定VEGFA为miR-140-5p的直接和功能靶基因。通过小干扰RNA(siRNA)沉默VEGFA类似于异位miR-140-5p表达所产生的表型,而VEGFA的过表达减弱了miR-140-5p对CRC细胞的作用。结论:我们的结果表明,miR-140-5p通过靶向VEGFA在CRC肿瘤发生和发展中具有抑癌作用。

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