癌变
癌症研究
癌基因
细胞生长
细胞
肺癌
抑制器
生物
肺
医学
癌症
病理
内科学
肿瘤科
细胞周期
生物化学
作者
Haitao Huang,Yuxuan Wang,Qin Li,Xiaoyan Fei,Haitao Ma,Rongkuan Hu
出处
期刊:Cancer Letters
[Elsevier BV]
日期:2019-01-17
卷期号:446: 81-89
被引量:67
标识
DOI:10.1016/j.canlet.2019.01.007
摘要
Squamous cell lung cancer (SqCLC) is among the most malignant lung cancers worldwide, lacking biomarkers for diagnostic and targets for treatment. In this study, we observed that miR-140-3p was expressed at low levels both in SqCLC cell lines and patient samples, while overexpression of miR-140-3p dramatically reduced the cell proliferation and invasion in SqCLC cells and Patient derived xenograft (PDX) models. Our further investigation indicated miR-140-3p negatively affected the tumorigenesis of SqCLC by down-regulating the expression of BRD9, an oncogene in SqCLC. Inhibition of BRD9 repressed SqCLC tumorigenesis by regulating c-myc expression. Meanwhile, BRD9 expression is up-regulated and negatively correlated with miR-140-3p in clinical samples; a meta-analysis of survival data indicates that SqCLC patients with high levels of BRD9 in their tumors have a worse prognosis. Collectively, our study suggests the prognostic and therapeutic roles of miR-140-3p and BRD9 axis in squamous cell lung cancer.
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