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miR-215 suppresses proliferation and migration of non-small cell lung cancer cells
被引:28
|作者:
Cai, Xiaopan
[1
]
Peng, Dongyu
[1
]
Wei, Haifeng
[1
]
Yang, Xinghai
[1
]
Huang, Quan
[1
]
Lin, Zaijun
[1
]
Xu, Wei
[1
]
Qian, Ming
[1
]
Yang, Cheng
[1
]
Liu, Tielong
[1
]
Yan, Wangjun
[1
]
Zhao, Jian
[1
]
机构:
[1] Second Mil Med Univ, Changzheng Hosp, Dept Bone Tumor Surg, 415 Fengyang Rd, Shanghai 200003, Peoples R China
关键词:
non-small cell lung cancer;
migration;
microRNA;
lung cancer;
miR-215;
TUMOR-SUPPRESSOR;
POOR-PROGNOSIS;
COLON-CANCER;
RISK-FACTORS;
EPIDEMIOLOGY;
DIAGNOSIS;
MICRORNA;
METASTASIS;
PATHWAY;
MARKER;
D O I:
10.3892/ol.2017.5692
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
The expression of microRNA-215 (miR-215) in non-small cell lung cancer (NSCLC) tissues and the effects of miR-215 on the proliferation and migration of NSCLC cells were investigated. qRT-PCR was used to detect the expression of miR-215 in NSCLC tissues and paired normal tumor-adjacent lung tissues; MTT assay, transwell assay and soft-agar assay were used in vitro to evaluate the role of miR-215 on proliferation, migration and cell clonality on NSCLC cells, after transfecting miR-215 mimics to NSCLC cell line A549 or miR-215 to H1299. miR-215 was significantly decreased in NSCLC tissues compared to the paired normal tissues; Overexpression of miR-215 in A549 cells resulted in reduction of the cell proliferation, migration and cell clonality, while downregulation of miR-215 in H1299 cells could promote cell proliferation, migration and clonality. In conclusion, miR-215 was downregulated in NSCLC tissues and may play a key role in the development of NSCLC.
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页码:2349 / 2353
页数:5
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