MicroRNA-30b inhibits non-small cell lung cancer cell growth by targeting the epidermal growth factor receptor

被引:17
作者
Qi, Z. [1 ]
Zhang, B. [2 ]
Zhang, J. [2 ]
Hu, Q. [2 ]
Xu, F. [1 ]
Chen, B. [2 ]
Zhu, C. [2 ]
机构
[1] Wenzhou Med Univ, Taizhou Hosp, Publ Lab, Affiliated Hosp, Taizhou, Zhejiang, Peoples R China
[2] Wenzhou Med Univ, Taizhou Hosp, Dept Cardiothorac Surg, Affiliated Hosp, Taizhou, Zhejiang, Peoples R China
关键词
miR-30b; non-small cell lung cancer; EGFR; proliferation; apoptosis; TUMOR-SUPPRESSOR; AMPLIFICATION; SURVIVAL; INVASION;
D O I
10.4149/neo_2018_170217N118
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Lung cancer, especially non-small cell lung cancer (NSCLC), is the leading cause of cancer-related mortality in the world. Both microRNAs and epidermal growth factor receptor (EGFR) are important factors in NSCLC. In our study, the expression of miR-30b in 47 tumor tissues and paired normal tissues of NSCLC were detected by RT-PCR, and we found that miR-30b was down-regulated in NSCLC tumor tissues and was associated with TNM stage, differentiation, and lymph node metastases. Then we investigated the ability of miR-30b to regulate EGFR in several NSCLC cell lines, and found that miR-30b inhibited proliferation, migration and invasion, induced apoptosis and enhanced sensitivity of the NSCLC cells to EGFR tyrosine kinase inhibitors (EGFR-TKIs) by targeting EGFR and repressing EGFR signaling pathways. Overall, these results indicate that miR-30b may be a potential therapeutic target in NSCLC patients.
引用
收藏
页码:192 / 200
页数:9
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