MiR-130 exerts tumor suppressive function on the tumorigenesis of human non-small cell lung cancer by targeting PTEN

被引:7
作者
Ye, Ling [1 ]
Wang, Yiming [1 ]
Nie, Lin [1 ]
Qian, Shen [2 ]
Xu, Meng [1 ]
机构
[1] Jinan Univ, Dept Oncol, Affiliated Hosp 1, 613 Huangpu Ave West Rd, Guangzhou, Guangdong, Peoples R China
[2] Armed Police Corps Hosp Guangdong Prov, Guangzhou, Guangdong, Peoples R China
来源
AMERICAN JOURNAL OF TRANSLATIONAL RESEARCH | 2017年 / 9卷 / 04期
关键词
Non-small cell lung cancer; miR-130; PTEN; proliferation; apoptosis; PANCREATIC-CANCER; NSCLC CELLS; PROLIFERATION; EXPRESSION; APOPTOSIS; SURVIVAL; AKT; MIGRATION; INVASION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) have been involved in some human malignancies and correlated with tumor progression. The dysregulation of miR-130 is found in various cancers and correlated with tumor proliferation and apoptosis. However, its expression and function in non-small cell lung cancer (NSCLC) have not been investigated yet. In this study, we demonstrated that miR-130 is significantly down-regulated in NSCLC tissue samples and cell lines. Low miR-130 expression was closely associated with lymph node metastasis, late stages of disease progression and diminished survival in NSCLC patients. The up-regulation of miR-130 could significantly inhibit NSCLC cell growth and enhance cell apoptosis both in vitro and in vivo. Whereas inhibition of miR-130 exerted opposite effects. Furthermore, dual-luciferase reporter assay confirmed that PTEN was regulated by miR-130 directly, and the knockdown of PTEN markedly abrogated the anti-growth effect of miR-130. Additionally, miR-130 was found positively correlated with PTEN in NSCLC specimens. In conclusion, our results suggested that the expression of miR-130 is significantly associated with the growth and apoptosis of NSCLS cells by targeting PTEN, whilst miR-130 may be a potential therapeutic target for NSCLC treatment.
引用
收藏
页码:1856 / 1865
页数:10
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