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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.
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页码:520 / 532
页数:13
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