MiR-15a suppresses hepatocarcinoma cell migration and invasion by directly targeting cMyb

被引:1
|
作者
Liu, Bo [1 ]
Sun, Ting [1 ]
Wu, Gang [1 ]
Hui Shang-Guan [2 ]
Jiang, Zhao-Jin [1 ]
Zhang, Ji-Ren [1 ]
Zheng, Yan-Fang [1 ]
机构
[1] Southern Med Univ, Oncol Ctr, Zhujiang Hosp, 253 Prov Ind Rd, Guangzhou 510282, Guangdong, Peoples R China
[2] Southern Med Univ, Dept Oncol, Foshan Hosp, Foshan 528000, Guangdong, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
miR-15a; Hepatocarcinoma; cMyb; EPITHELIAL-MESENCHYMAL TRANSITION; HEPATOCELLULAR-CARCINOMA CELLS; CANCER STEM-CELLS; C-MYB; COLORECTAL-CANCER; MESSENGER-RNA; UP-REGULATION; MICRORNAS; IDENTIFICATION; EXPRESSION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: This study aimed to determine the function of miR-15a in HCC, and identify cMyb as a target of miR-15a. Methods: RNA expression was evaluated by quantitative real-time PCR (qRT-PCR). The effects of miR-15a or cMyb on HCC cells were evaluated by transwell migration assay and western blot analysis. CMyb, the predicted target, has been frequently verified by luciferase assay. Results: MiR-15a was markedly downregulated in sphere culture HCC cells by qRT-PCR. CMyb was predicted to be a potential target of miR-15a using bioinformatics analysis. This prediction has been frequently verified by luciferase assay and western blot. A positive correlation between cMyb and the migration ability of HCC cells was demonstrated by transwell assays. MiR-15a mimic suppressed cMyb expression to weaken HCC cell migration ability. On the other hand, miR-15a inhibitor upregulated cMyb and induced HCC cell migration. Conclusion: MiR-15a could suppress HCC progression through the repression of cMyb, making miR-15a a potential therapeutic target.
引用
收藏
页码:520 / 532
页数:13
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