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RETRACTED: Hsa-miR-337 inhibits non-small cell lung cancer cell invasion and migration by targeting TCF7 (Retracted Article)
被引:10
|作者:
Zhang, J.
[1
]
Gong, W-H
[2
]
Li, Y.
[3
]
Zhang, H-Y
[4
]
Zhang, C-X
[1
]
机构:
[1] Dalian Med Univ, Affiliated Hosp 1, Dept Oncol, Dalian, Peoples R China
[2] Suizhou Cent Hosp, Dept Ultrasonog, Suizhou, Peoples R China
[3] Guizhou Med Univ, Affiliated Hosp, Guiyang, Guizhou, Peoples R China
[4] Dalian Med Univ, Coll Basic Med Sci, Dept Pathol & Forens Med, Dalian, Peoples R China
基金:
中国国家自然科学基金;
关键词:
MicroRNA;
Hsa-miR-337;
NSCLC;
TCF7;
COLORECTAL-CANCER;
UP-REGULATION;
METASTASIS;
PROMOTES;
GROWTH;
PROLIFERATION;
D O I:
10.26355/eurrev_201908_18540
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
OBJECTIVE: Recent studies have revealed that microRNAs (miRNAs) play a crucial role in the progression of tumorigenesis. Non-small cell lung cancer (NSCLC) is one of the most common malignancies worldwide. The aim of this study was to identify the exact role of hsa-miR-337 in the progression of NSCLC and to investigate the possible underlying mechanism. PATIENTS AND METHODS: Hsa-miR-337 expression in NSCLC cells and 60 paired tissue samples were detected by Real Time-quantitative Polymerase Chain Reaction (RT-qPCR). Moreover, the functions of hsa-miR-337 in vitro were identified by transwell assay and wound healing assay, respectively. Furthermore, the underlying mechanism was explored by RT-qPCR, Western blot assay, and luciferase assay. RESULTS: The expression level of hsa-miR-337 in NSCLC tissues was remarkably down-regulated when compared with that of adjacent normal samples. Moreover, the invasion and migration of NSCLC cells were significantly inhibited after overexpression of hsa-miR-337 in vitro. Moreover, after overexpression of hsa-miR-337 in vitro, the mRNA and protein levels of TCF7 were significantly down-regulated. Besides, the expression of TCF7 in NSCLC tissues was negatively correlated with the expression of hsa-miR-337. CONCLUSIONS: The above results suggested that hsa-miR-337 could repress the migration and invasion of NSCLC cells through directly targeting TCF7. Furthermore, hsa-miR-337 might offer a new therapeutic intervention for NSCLC patients.
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页码:6548 / 6553
页数:6
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