miR-338 inhibits the metastasis of lung cancer by targeting integrin 3

被引:17
作者
Chen, Xiao [1 ]
Wei, Li [2 ]
Zhao, Song [1 ]
机构
[1] Zhengzhou Univ, Dept Thorac Surg, Affiliated Hosp 1, Zhengzhou 450003, Henan, Peoples R China
[2] Peoples Hosp Henan Prov, Dept Thorac Surg, Zhengzhou 450003, Henan, Peoples R China
关键词
lung cancer; miRNAs; miR-338; ITGB3; metastasis; DIFFERENTIAL EXPRESSION; UP-REGULATION; MICRORNAS; PROMOTES; ITGB3; OVEREXPRESSION; ADENOCARCINOMA; TUMORIGENESIS; MIGRATION; BIOMARKER;
D O I
10.3892/or.2016.4928
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
miR-338 as an intronic miRNA from apoptosis-associated tyrosine kinase (AATK) is involved in tumor proliferation and apoptosis, but its function and regulatory mechanism in lung cancer is still obscure. In the present study, we found that miR-338 was strikingly downregulated in 115 lung cancer tissues and 5 lung cancer cell lines. Besides, low level of miR-338 was associated with tumor emboli, TNM stage, tumor recurrence and poor survival. Regaining the expression of miR-338 in lung cancer cell lines significantly impaired cellular adhesion, migration, invasion and lung tumor formation in nude mice. Furthermore, we also identified a metastasis related protein, integrin 3 (ITGB3), as a novel target gene of miR-338. Our results reveal a new regulatory mechanism of miR-338 which may help us better understand the metastasis of lung cancer.
引用
收藏
页码:1467 / 1474
页数:8
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