Circular RNA hsa_circ_0026344 suppresses gastric cancer cell proliferation, migration and invasion via the miR-590-5p/PDCD4 axis.

Long Lv, Jinghu Du, Daorong Wang, Zeqiang Yan
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引用次数: 3

Abstract

OBJECTIVES Circular RNA (CircRNA) is a class of non-coding RNA transcripts, with multiple pathophysiological functions. Instead, the mechanism and function of circRNA in gastric cancer (GC) are not fully deciphered. METHODS CircRNA_0026344 (circ_0026344), microRNA (miR)-590-5p and programmed cell death 4 (PDCD4) mRNA expression levels in GC tissues and cells were probed by quantitative real-time PCR. Cell viability, migration and aggressiveness were examined by cell counting kit-8 and transwell assays. Additionally, the interplay among circ_0026344, miR-590-5p and PDCD4 was verified with bioinformatics and dual-luciferase reporter gene assay. Western blot was conducted to probe PDCD4 protein expression. KEY FINDINGS Circ_0026344 expression was underexpressed in GC tissues and cells, which was associated with clinicopathological characteristics such as tumour size, tumor-node-metastasis stage and lymph node metastasis. Circ_0026344 overexpression restrained the malignant biological behaviours of GC cells, while circ_0026344 knockdown functioned oppositely. Circ_0026344 could act as a competing endogenous RNA of miR-590-5p to negatively modulate its expression, and this miRNA could mitigate the impact of circ_0026344 on GC cells. In addition, PDCD4 was identified as the downstream target of miR-590-5p, and PDCD4 expression was positively modulated by circ_0026344. CONCLUSIONS Circ_0026344 up-regulates PDCD4 expression via sponging miR-590-5p, thus inhibiting the progression of GC. This study further expounds the underlying molecular mechanism in the GC progression.
环状RNA hsa_circ_0026344通过miR-590-5p/PDCD4轴抑制胃癌细胞增殖、迁移和侵袭。
目的环状RNA (CircRNA)是一类非编码RNA转录物,具有多种病理生理功能。相反,circRNA在胃癌(GC)中的机制和功能尚未完全破译。方法采用实时荧光定量PCR检测GC组织和细胞中scircrna_0026344 (circ_0026344)、microRNA (miR)-590-5p和程序性细胞死亡4 (PDCD4) mRNA的表达水平。采用细胞计数试剂盒-8和transwell检测细胞活力、迁移和侵袭性。此外,通过生物信息学和双荧光素酶报告基因测定验证了circ_0026344、miR-590-5p和PDCD4之间的相互作用。Western blot检测PDCD4蛋白表达。关键发现scirc_0026344在胃癌组织和细胞中低表达,与肿瘤大小、肿瘤-淋巴结-转移分期、淋巴结转移等临床病理特征相关。Circ_0026344过表达抑制GC细胞的恶性生物学行为,而Circ_0026344敲低则相反。Circ_0026344可以作为miR-590-5p的竞争内源性RNA负向调节其表达,该miRNA可以减轻Circ_0026344对GC细胞的影响。此外,PDCD4被鉴定为miR-590-5p的下游靶点,并且circ_0026344正向调节PDCD4的表达。结论scirc_0026344通过海绵细胞miR-590-5p上调PDCD4的表达,从而抑制胃癌的进展。本研究进一步阐明了GC过程的潜在分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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