miR-3120-5p acts as a diagnostic biomarker in non-small cell lung cancer and promotes cancer cell proliferation and invasion by targeting KLF4

被引:8
|
作者
Xu, Hongwei [1 ]
Wen, Quan [2 ]
机构
[1] Harbin Med Univ, Affiliated Hosp 2, Clin Lab, 248 Xuefu Rd, Harbin 150086, Heilongjiang, Peoples R China
[2] Harbin Med Univ, Affiliated Hosp 4, Gen Internal Med Lab, Harbin 150001, Heilongjiang, Peoples R China
关键词
microRNA-3120-5p; non-small cell lung cancer; proliferation; invasion; Krueppel-like factor 4; EPITHELIAL-MESENCHYMAL TRANSITION; GROWTH; METASTASIS; REPRESSION;
D O I
10.3892/mmr.2018.9454
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Accumulating evidence indicates that microRNAs (miRs) are important regulators in a number of types of human cancer, including non-small cell lung cancer (NSCLC). The function of miR-3120-5p in NSCLC remains unclear. In the present study, it was demonstrated that miR-3120-5p was significantly upregulated in NSCLC tissues. Additionally, miR-3120-5p expression level was positively associated with NSCLC metastasis and tumor, node and metastasis stage. Furthermore, it was demonstrated that miR-3120-5p exhibited potential as an indicator of NSCLC for use in diagnosis. Through functional experiments, it was demonstrated that overexpression of miR-3120-5p promoted the proliferation, colony formation and invasion of NSCLC cells. miR-3120-5p overexpression significantly promoted cell cycle progression. Mechanistically, it was demonstrated that Krueppel-like factor 4 (KLF4) was a target of miR-3120-5p in NSCLC cells. Overexpression of miR-3120-5p repressed the expression of KLF4 in A549 and H460 cells. Furthermore, it was demonstrated that KLF4 was downregulated in NSCLC tissues and cell lines. Overexpression of KLF4 significantly reversed the effects of miR-3120-5p on NSCLC cell proliferation and invasion. In conclusion, the present study demonstrated that miR-3120-5p promoted NSCLC progression by directly targeting KLF4.
引用
收藏
页码:4621 / 4628
页数:8
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