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MiR-454 promotes the progression of human non-small cell lung cancer and directly targets PTEN
被引:62
|作者:
Zhu Deng-Yan
[1
]
Li Xiang-Nan
[1
]
Yu, Qi
[1
]
Liu Dong-Lei
[1
]
Yang, Yang
[1
]
Jia, Zhao
[1
]
Zhang Chun-Yang
[1
]
Kai, Wu
[1
]
Song, Zhao
[1
]
机构:
[1] Zhengzhou Univ, Affiliated Hosp 1, Dept Thorac Surg, 1 East Jianshe Rd, Zhengzhou 450052, Henan, Peoples R China
关键词:
MiR-454;
Non-small cell lung cancer;
PTEN;
Prognosis;
Proliferation;
Apoptosis;
PROLIFERATION;
EXPRESSION;
ONCOGENE;
INVASION;
D O I:
10.1016/j.biopha.2016.03.029
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:
Purpose: MicroRNA-454 has been proven dysregulated in some human malignancies and correlated with tumor progression. However, its expression and function in non-small cell lung cancer (NSCLC) is still unclear. Thus, the aim of this study was to explore the effects of miR-454 in NSCLC tumorigenesis and development. Methods: Using quantitative RT-PCR, we detected miR-454 expression in NSCLC cell lines and primary tumor tissues. The association of miR-454 expression with clinicopathological factors and prognosis was also analyzed. Then, the effects of miR-454 on the biological behavior of NSCLC cells were investigated. At last, the potential regulatory function of miR-454 on PTEN expression was confirmed. Results: miR-454 was found to be up-regulated in NSCLC tissues and cell lines. High miR-454 expression was closely correlated with lymph node metastasis, advanced TNM stage, and shorter overall survival. Multivariate regression analysis corroborated that miR-454 overexpression was an independent unfavourable prognostic factor for patients with NSCLC. Down-regulation of miR-454 could significantly reduce NSCLC cell proliferation, enhance cell apoptosis, and impair cell invasion and migration in vitro, while up-regulation of miR-454 showed opposite effects. Further, PTEN was confirmed as a direct target of miR-454 by using Luciferase Reporter Assay. Conclusions: These findings indicate that miR-454 may act as an oncogene in NSCLC and would serve as a potential therapy target for this disease. a 2016 Elsevier Masson SAS. All rights reserved.
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页码:79 / 85
页数:7
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