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RETRACTED: MicroRNA-629 inhibition suppresses the viability and invasion of non-small cell lung cancer cells by directly targeting RUNX3 (Retracted article. See vol. 27, 2023)
被引:4
|作者:
Zhuang, Bufeng
[1
]
Cheng, Youshuang
[1
]
机构:
[1] Shanghai Jiao Tong Univ, Sch Med, Shanghai Peoples Hosp 9, Dept Thorac Surg, 280 Mohe Rd, Shanghai 201900, Peoples R China
关键词:
non-small cell lung cancer;
microRNA-629;
runt-related transcription factor 3;
proliferation;
invasion;
PROGRESSION;
EXPRESSION;
PROLIFERATION;
INVOLVEMENT;
CARCINOMA;
PROTEIN;
TUMORS;
D O I:
10.3892/mmr.2019.9990
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Dysregulated microRNAs (miRNAs/miRs) directly modulate the biological functions of non-small cell lung cancer (NSCLC) cells and contribute to the initiation and progression of NSCLC; however, the specific roles and underlying mechanisms of the dysregulated miRNAs in NSCLC require further investigation. The present study reported that miRNA-629-5p (miR-629) was upregulated in NSCLC tissues and cell lines. High miR-629 expression levels were significantly associated with tumour size, clinical stage and lymph node metastasis in patients with NSCLC. Functional experiments indicated that miR-629 inhibition suppressed the viability and invasion NSCLC cells in vitro. Furthermore, bioinformatics prediction, luciferase reporter assay, reverse transcription-quantitative polymerase chain reaction and western blot analysis demonstrated that runt-related transcription factor 3 (RUNX3) was a direct target gene of miR-629 in NSCLC. Restoration of RUNX3 expression suppressed the effects of miR-629 inhibition in NSCLC cells. Rescue experiments revealed that RUNX3 knockdown partially abrogated the effects of miR-629 inhibition on NSCLC cells. In summary, miR-629 directly targeted RUNX3 to inhibit the progression of NSCLC, suggesting that this miRNA may be considered as a diagnostic and therapeutic target for patients with NSCLC.
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页码:3933 / 3940
页数:8
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