miR-544a promotes the invasion of lung cancer cells by targeting cadherina I in vitro

被引:22
作者
Mo, Xiaomei [1 ,2 ]
Zhang, Fenghua [2 ]
Liang, Hui [2 ]
Liu, Ming [1 ]
Li, Huahui [3 ]
Xia, Haiping [3 ]
机构
[1] Ocean Univ China, Sch Med & Pharm, Minist Educ, Key Lab Marine Drugs, Qingdao, Peoples R China
[2] Qingdao Women & Children Hosp, Qingdao, Peoples R China
[3] Qingdao Municipal Hosp, Dept Lab Med, Qingdao, Peoples R China
关键词
NSCLC; non-small cell lung cancer; E-cadherin; microRNA; EMT;
D O I
10.2147/OTT.S61695
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Objective: To find out the effect of miR-544a on the invasion of lung cancer cells and to explore the underlying molecular mechanisms. Methods: Micro-ribonucleic acid (miRNA) expression in two different invasive lung cancer cell lines 95C (low invasive ability) and 95D (high invasive ability) was analyzed by miRNA microarray and real-time quantitative -polymerase chain reaction (PCR); miR-544a mimic was transfected to 95C, and its invasion ability was detected by transwell migration assay; we predicted the candidate miRNA target genes by TargetScan (Whitehead Institute for Biomedical Research, Cambridge, MA, USA) software and verified the target genes by Western blot. Results: The expression of miR-544a was significantly increased in 95D in miRNA -microarray and quantitative PCR tests (P< 0.05). After being transfected with miR-544a mimic, the invasion ability of 95C was enhanced (P< 0.01). Moreover, transfection with miR-544a inhibitor decreased the invasion ability of 95D (P< 0.01). miR-544a possibly combined with CDH1 (E-cadherin) predicted by the TargetScan analysis. 95C with miR-544a mimic reduced the expression of CDH1 and improved the expression of vimentin, while 95D with miR-544a inhibitor improved the expression of CDH1 and reduced the expression of vimentin. Conclusion: miR-544a can promote the invasion of non-small cell lung cancer by downregulation of CDH1 and upregulation of vimentin.
引用
收藏
页码:895 / 900
页数:6
相关论文
共 9 条
[1]   miRNA-200c increases the sensitivity of breast cancer cells to doxorubicin through the suppression of E-cadherin-mediated PTEN/Akt signaling [J].
Chen, Yong ;
Sun, Ying ;
Chen, Longbang ;
Xu, Xingxiang ;
Zhang, Xizhi ;
Wang, Buhai ;
Min, Lingfeng ;
Liu, Wei .
MOLECULAR MEDICINE REPORTS, 2013, 7 (05) :1579-1584
[2]   MicroRNAs in the Imprinted DLK1-DIO3 Region Repress the Epithelial-to-Mesenchymal Transition by Targeting the TWIST1 Protein Signaling Network [J].
Haga, Christopher L. ;
Phinney, Donald G. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (51) :42695-42707
[3]   Lung cancer: Future directions [J].
Lam, Wah K. ;
Watkins, D. Neil .
RESPIROLOGY, 2007, 12 (04) :471-477
[4]   Downregulation of miR-544 in tissue, but not in serum, is a novel biomarker of malignant transformation in glioma [J].
Ma, Ruimin ;
Zhang, Guojun ;
Wang, Huimin ;
Lv, Hong ;
Fang, Fang ;
Kang, Xixiong .
ONCOLOGY LETTERS, 2012, 4 (06) :1321-1324
[5]  
Mo XM, 2014, ONCOL LETT IN PRESS
[6]   Control of metastatic progression by microRNA regulatory networks [J].
Pencheva, Nora ;
Tavazoie, Sohail F. .
NATURE CELL BIOLOGY, 2013, 15 (06) :546-554
[7]   Tumor Dissemination: An EMT Affair [J].
Thiery, Jean Paul ;
Lim, Chwee Teck .
CANCER CELL, 2013, 23 (03) :272-273
[8]   Regulation of Breast Cancer and Bone Metastasis by MicroRNAs [J].
Vimalraj, S. ;
Miranda, P. J. ;
Ramyakrishna, B. ;
Selvamurugan, N. .
DISEASE MARKERS, 2013, 2013 :369-387
[9]   Oncogenic miR-544 is an Important Molecular Target in Gastric Cancer [J].
Zhi, Qiaoming ;
Guo, Xiaobo ;
Guo, Lei ;
Zhang, Rongjuan ;
Jiang, Jinling ;
Ji, Jun ;
Zhang, Jianian ;
Zhang, Jun ;
Chen, Xuehua ;
Cai, Qu ;
Li, Jianfang ;
Liu, Bingya ;
Zhu, Zhenggang ;
Yu, Yingyan .
ANTI-CANCER AGENTS IN MEDICINAL CHEMISTRY, 2013, 13 (02) :270-275