MicroRNA-429 inhibits cancer cell proliferation and migration by targeting AKT1 in renal cell carcinoma

被引:19
作者
Su, Zhengming [1 ,2 ]
Jiang, Ganggang [1 ,3 ]
Chen, Jinlan [1 ]
Liu, Xing [1 ]
Zhao, Haibo [1 ]
Fang, Zhiyuan [3 ]
He, Yongzhong [1 ]
Jiang, Xianhan [1 ,2 ]
Xu, Guibin [1 ,2 ]
机构
[1] Guangzhou Med Univ, Dept Urol, Affiliated Hosp 5, 621 Gangwan Rd, Guangzhou 510700, Guangdong, Peoples R China
[2] Guangzhou Med Univ, Ctr Innovat & Translat Minimally Invas Tech, Guangzhou 510700, Guangdong, Peoples R China
[3] Guangzhou Med Univ, Dept Ctr Lab, Affiliated Hosp 5, Guangzhou 510700, Guangdong, Peoples R China
关键词
renal cell carcinoma; AKT serine; threonine kinase 1; microRNA-429; EPITHELIAL OVARIAN-CANCER; HEPATOCELLULAR-CARCINOMA; DOWN-REGULATION; POOR-PROGNOSIS; MIR-429; EXPRESSION; INVASION; METASTASIS; MECHANISM; GENE;
D O I
10.3892/mco.2019.1940
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs or miR) serve as oncogenes and tumor suppressors. In a previous study, it was revealed that has-miRNA-429 (miR-429) is a tumor suppressor in 786-O renal cell carcinoma (RCC) cells. However, its mechanism in RCC remains to be determined. The present study aimed to explain the functional role and mechanism of miR-429 in RCC pathogenesis. Luciferase reporter assays demonstrated that miR-429 overexpression reduced the transcriptional activity of AKT serine/threonine kinase 1 (AKT1). Reverse transcripton-quantitative (RT-q) PCR and western blot analysis indicated that the mRNA and protein expression of AKT1 was downregulated in 786-O RCC cell lines when miR-429 was overexpressed, indicating that miR-429 may directly target AKT1 in RCC. Therefore, miR-429 overexpression enhanced the inhibition of tumor size and weight in nude mice in vivo. The current study indicated that the novel miR-429-regulated pathway may provide insights into RCC oncogenesis and metastasis.
引用
收藏
页码:75 / 80
页数:6
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