MicroRNA-187 modulates epithelial-mesenchymal transition by targeting PTRF in non-small cell lung cancer

被引:28
|
作者
Cai, Yanjun [1 ,2 ]
Ruan, Jian [3 ]
Yao, Xueqing [4 ]
Zhao, Liang [5 ]
Wang, Baocheng [1 ,6 ]
机构
[1] Second Mil Med Univ, Jinan Clin Coll, Dept Oncol, Jinan, Shandong, Peoples R China
[2] Guangzhou Mil Command PLA, Gen Hosp, Dept Geriatr, Guangzhou, Guangdong, Peoples R China
[3] Southern Med Univ, Canc Ctr, Tradit Chinese Med Integrated Hosp, Guangzhou, Guangdong, Peoples R China
[4] Guangdong Acad Med Sci, Guangdong Gen Hosp, Dept Gen Surg, Guangzhou, Guangdong, Peoples R China
[5] Southern Med Univ, Sch Basic Med Sci, Dept Pathol, Guangzhou, Guangdong, Peoples R China
[6] Jinan Mil Command PLA, Gen Hosp, Dept Oncol, Jinan, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
non-small cell lung cancer; epithelial-mesenchymal transition; polymerase I and transcript release factor; PTRF; microRNAs; tumor metastasis; TRANSCRIPT RELEASE FACTOR; DOWN-REGULATION; GROWTH; PROGRESSION; EXPRESSION; METASTASIS; ACTIVATION; CAVEOLIN-1; CARCINOMA; PATTERNS;
D O I
10.3892/or.2017.5548
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) that negatively regulate gene expression play a key role in the development and progression of cancer. Aberrant expression of hsa-miR-187 (miR-187) has been reported in various malignancies. However, the function of miR-187 in tumor progression remains controversial and its role in non-small cell lung cancer (NSCLC) is poorly understood. In the present study, the role of miR-187 in the progression of NSCLC was investigated. Our results revealed that miR-187 was frequently upregulated in NSCLC tissues and cells. Furthermore, ectopic introduction of miR-187 promoted cell migration, whereas miR-187 inhibitor had the contrary effect in NSCLC cells. Of significance, miR-187 induced epithelial-mesenchymal transition (EMT), which plays a pivotal role in the initiation of metastasis and activated mitogen-activated protein kinase (MAPK) and phosphatidylinositol-3-kinase/protein kinase B (PI3K/AKT) pathways. Polymerase I and transcript release factor (PTRF) was identified as a direct target of miR-187 in the promotion of the migration of NSCLC cells. Restored expression of PTRF neutralized the promoting effect of miR-187 on cell migration and EMT of NSCLC cells. Collectively, our data highlight the pivotal role of miR-187 in the progression of NSCLC, indicating this factor as a potential candidate in molecular cancer therapy.
引用
收藏
页码:2787 / 2794
页数:8
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