MicroRNA-30a regulates cell proliferation, migration, invasion and apoptosis in human nasopharyngeal carcinoma via targeted regulation of ZEB2

被引:12
作者
Chen, Xi [1 ]
Li, Junzheng [2 ]
Zhang, Shifen [3 ]
Xu, Weiping [4 ]
Shi, Dianyu [1 ]
Zhuo, Mugai [4 ]
Liang, Shaoqin [4 ]
Lei, Wenbin [5 ]
Xie, Chun [6 ]
机构
[1] Peoples Hosp Longhua, Dept Otorhinolaryngol, Shenzhen 518109, Guangdong, Peoples R China
[2] Jinan Univ, Affiliated Dongguan Hosp, Dept Otolaryngol, Dongguan 523905, Guangdong, Peoples R China
[3] Jinan Univ, Clin Med Coll 2, Shenzhen Peoples Hosp, Dept Pathol, Shenzhen 518020, Guangdong, Peoples R China
[4] Third Peoples Hosp Longgang, Dept Otorhinolaryngol, Shenzhen 518115, Guangdong, Peoples R China
[5] Sun Yat Sen Univ, Affiliated Hosp 1, Otorhinolaryngol Hosp, Dept Otorhinolaryngol, 58 Zhongshan Rd 2, Guangzhou 510080, Guangdong, Peoples R China
[6] Peoples Hosp Longhua, Dept Stomatol, 38 Jinglong Construct Rd, Shenzhen 518109, Guangdong, Peoples R China
关键词
microRNA30a; zinc finger E-box binding homeobox 2; nasopharyngeal carcinoma; cell viability; cell apoptosis; STEM-CELLS; CANCER; METASTASIS; SUPPRESSES; EXPRESSION; MIR-30A-5P; SURVIVAL; IGF-1;
D O I
10.3892/mmr.2019.10387
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNA-30a (miR-30a) was previously reported to serve as a tumor suppressor able to inhibit the development and progression of certain types of cancer. A number of previous studies demonstrated that zinc finger E-box binding homeobox 2 (ZEB2) may be regulated by miR-30a in clear cell renal cell carcinoma and breast cancer. However, the function of miR-30a in human nasopharyngeal carcinoma (NPC) remains unclear. The present study aimed to investigate the association between miR-30a and ZEB2 in NPC. Therefore, the expression levels of miR-30a and ZEB2 were measured in human NPC cells and tissues from patients with NPC, and the present results suggested that the expression level of miR-30a was significantly decreased in NPC tissues compared with paracancerous tissues. The direct interaction between miR-30a and the untranslated region of ZEB2 was examined using the dual-luciferase reporter assay, and ZEB2 was identified as a direct target of miR-30a. Additionally, the effects of miR-30a and ZEB2 overexpression on cell proliferation, migration, invasion and apoptosis were additionally investigated. Functional experiments identified that overexpression of miR-30a increased apoptosis and suppressed cell proliferation, cell migration and cell invasion by directly targeting ZEB2. Collectively, the present study suggested that miR-30a may serve an important role in the progression of NPC and may represent a novel target for the treatment of patients with NPC.
引用
收藏
页码:1672 / 1682
页数:11
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