MiR-424-5p promotes cell invasion and migration by targeting CYLD in human pancreatic cancer

被引:0
|
作者
Xu, Xiao Yong [1 ,3 ]
Yan, Wei Juan [2 ]
Jiang, Wei Ming [3 ]
Wang, Jin [3 ]
Yang, Jie [3 ]
Lv, Wei [3 ]
Li, Chun Ming [4 ]
Zhou, Ding Hua [3 ]
机构
[1] Soochow Univ, Coll Med, Ind Pk, Suzhou 215123, Jiangsu, Peoples R China
[2] Gen Hosp PLA Second Artillery, Dept Cent Lab, Beijing 100088, Peoples R China
[3] Gen Hosp PLA Second Artillery, Dept Hepatobiliary Surg, 16 Xinjiekouwai Ave, Beijing 100088, Peoples R China
[4] Capital Med Univ, Beijing Chao Yang Hosp, Dept Vasc Surg, 8 Gongren Tiyuchang Nanlu, Beijing 100020, Peoples R China
关键词
CYLD; invasion; migration; MiR-424-5p; pancreatic cancer; MESENCHYMAL TRANSITION; DOWN-REGULATION; EXPRESSION; MICRORNAS; BETA; IDENTIFICATION; INACTIVATION; METASTASIS; ROLES;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The effect and mechanism of miR-424-5p on the invasion and migration of human pancreatic cancer is unknown. Quantitative real-time PCR (qRT-PCR) was performed to detect the expression of miR-424-5p and CYLD in pancreatic cancer specimens and pancreatic cancer cells PANC-1. MiR-424-5p mimics/inhibitors and their negative controls were transfected into PANC-1 cells respectively, following by transwell, and wound healing assays, which were used for investigating the capacity of cell invasion and migration. Meanwhile, protein levels of CYLD, Smad3 and E-cadherin were examined through western blotting. Luciferase reporter assay was used to validate CYLD as a target of miR-424-5p. MiR-424-5p suppressed the expression of CYLD and was significantly upregulated in pancreatic cancer specimens and cells. Overexpression of miR-424-5p promoted cell invasion and migration, which on the contrary would be reduced by the downregulation of miR-424-5p in vitro. MiR-424-5p may increase pancreatic cancer cells invasion and migration by targeting CYLD, and thus potentially serving as a new therapeutic target for pancreatic cancer.
引用
收藏
页码:5960 / 5968
页数:9
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