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MicroRNA-140-5p suppresses cell proliferation and invasion in gastric cancer by targeting WNT1 in the WNT/β-catenin signaling pathway

机译:MicroRNA-140-5p通过在WNT /β-catenin信号通路中靶向WNT1抑制胃癌细胞的增殖和侵袭

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摘要

MicroRNAs have been suggested as potential regulators in gastric cancer (GC) development through affecting the expression of their target genes. Previous studies have demonstrated that miR-140-5p is downregulated in GC. However, the underlying functional role of miR-140-5p in GC remains largely unknown. The present study revealed that miR-140-5p expression was significantly decreased in 60 GC tissues, compared with corresponding adjacent non-tumor tissues. A lower miR-140-5p expression was significantly associated with lymph node metastasis and an advanced Tumor-Node-Metastasis stage in patients with GC. Furthermore, patients with a lower miR-140-5p expression exhibited shorter disease-free survival and overall survival times. Gain- and loss-of-function assays revealed that increased miR-140-5p expression significantly inhibited GC cell proliferation and invasion ability, as well as the Wnt/β-catenin signaling pathway by decreasing WNT1 and β-catenin expression. However, decreasing miR-140-5p expression had the opposite effects. Bioinformatics methods and dual-luciferase reporter assays revealed that WNT1 was a direct target of miR-140-5p. miR-140-5p suppressed cell proliferation and invasion by regulating WNT1 expression. Therefore, the results of the present study demonstrated that miR-140-5p may serve as a potential prognostic marker and therapeutic target in patients with GC.
机译:有人建议通过影响其靶基因的表达,将微小RNA作为胃癌(GC)发育的潜在调控因子。先前的研究表明,miR-140-5p在GC中被下调。但是,miR-140-5p在GC中的潜在功能仍是未知之数。本研究表明,与相应的邻近非肿瘤组织相比,在60个GC组织中miR-140-5p表达显着降低。较低的miR-140-5p表达与GC患者的淋巴结转移和晚期肿瘤结点转移阶段显着相关。此外,miR-140-5p表达较低的患者表现出较短的无病生存期和总生存期。功能获得和功能丧失试验表明,增加的miR-140-5p表达可通过降低WNT1和β-catenin表达来显着抑制GC细胞的增殖和侵袭能力以及Wnt /β-catenin信号通路。但是,降低miR-140-5p表达具有相反的效果。生物信息学方法和双重荧光素酶报告基因检测表明,WNT1是miR-140-5p的直接靶标。 miR-140-5p通过调节WNT1表达来抑制细胞增殖和侵袭。因此,本研究的结果证明,miR-140-5p可以作为GC患者的潜在预后标志物和治疗靶标。

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