Role of miR-497 in VEGF-A-mediated cancer cell growth and invasion in non-small cell lung cancer

被引:36
作者
Gu, Aiqin [1 ]
Lu, Jianhong [2 ]
Wang, Weimin [1 ]
Shi, Chunlei [1 ]
Han, Baohui [1 ]
Yao, Ming [3 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Chest Hosp, Dept Pulm Med, 241 Huaihai Rd, Shanghai 200030, Peoples R China
[2] Shanghai Jiao Tong Univ, Shanghai Gen Hosp, Int Med Care Ctr, Shanghai 200080, Peoples R China
[3] Shanghai Jiao Tong Univ, Sch Med, Renji Hosp, State Key Lab Oncogenes & Related Genes,Shanghai, 25-Ln 2200 Xietu Rd, Shanghai 200032, Peoples R China
关键词
Non-small cell lung cancer (NSCLC); Vascular endothelial growth factor A (VEGF-A); MiR-497; Bioinformatics analyses; MiRNAs; IN-VITRO; LYMPHOVASCULAR INVASION; ENDOTHELIAL-CELLS; MMP9; ACTIVATION; INHIBITS GROWTH; GASTRIC-CANCER; METASTASIS; NEOVASCULARIZATION; PHOSPHORYLATION; GLIOBLASTOMA;
D O I
10.1016/j.biocel.2015.10.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The malignancy of non-small cell lung cancer (NSCLC) is largely due to its invasion. Hence, prevention of the cancer cell invasion, which is essentially regulated by vascular endothelial growth factor A (VEGF-A), is substantially critical for a successful treatment for NSCLC. Here, we showed that compared to other cancers, NSCLC had a significant higher ratio of VEGF-A protein vs mRNA, and significantly lower levels of miR-497, suggesting presence of a post-transcriptional control of VEGF-A in NSCLC different from other cancers. Compared with paired normal lung tissue, NSCLC expressed lower levels of miR-497 and higher levels of VEGF-A. Moreover, the levels of miR-497 and VEGF-A were inversely correlated in NSCLC specimen. Bioinformatics analyses showed that miR-497 bound to 3'-UTR of VEGF-A mRNA in NSCLC lines to inhibit its translation. Overexpression of miR-497 in NSCLC lines decreased VEGF-A protein, while depletion of miR-497 in NSCLC lines increased VEGF-A protein. However, modification of miR-497 levels in NSCLC lines did not alter VEGF-A mRNA levels. Overexpression of miR-497 in NSCLC lines inhibited cell growth and invasion, while depletion of miR-497 in NSCLC lines increased cell growth and invasion. Together, our data demonstrate a previously unappreciated role for miR-497 in suppression of VEGF-A-mediated NSCLC cancer cell growth and invasion. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:118 / 125
页数:8
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