MicroRNA-590 Promotes Cervical Cancer Cell Growth and Invasion by Targeting CHL1

被引:86
作者
Chu, Yanxia [1 ]
Ouyang, Yunwei [1 ]
Wang, Fei [1 ]
Zheng, Ai [1 ]
Bai, Liping [1 ]
Han, Ling [1 ]
Chen, Yali [1 ]
Wang, Hui [1 ]
机构
[1] Sichuan Univ, West China Second Univ Hosp, Dept Obstetr & Gynecol, Chengdu 610041, Peoples R China
关键词
miR-590-5p; CHL1; CERVICAL CANCER; CELL INVASION; CELL CYCLE; PROLIFERATION;
D O I
10.1002/jcb.24726
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
MicroRNAs (miRNAs) may function as oncogenes or tumor suppressors. Here, we identified that miR-590-5p was up-regulated in human cervical cancer. Over-expression of miR-590-5p promoted cervical cancer cell growth, cell cycle and invasion via Growth curve, Colony formation, FACS and Transwell assays in HeLa and C33A cell lines. Subsequently, CHL1 was identified as a potential miR-590-5p target by bioinformatics analysis. Moreover, we showed that CHL1 was negatively regulated by miR-590-5p at the posttranscriptional level, via a specific target site within the 3UTR by luciferase reporter assay. Furthermore, the mRNA and protein levels of CHL1 in cervical cancer cells were downregulated by miR-590-5p. And we identified the cell phenotype altered by miR-590-5p can be rescued by over-expression of CHL1. Therefore, our findings suggest that miR-590-5p acts as an oncogene by targeting the CHL1 gene and promotes cervical cancer proliferation. The findings of this study contribute to current understanding of the functions of miR-590-5p in cervical cancer. J. Cell. Biochem. 115: 847-853, 2014. (c) 2013 Wiley Periodicals, Inc.
引用
收藏
页码:847 / 853
页数:7
相关论文
共 23 条
[1]   MicroRNAs miR-30b, miR-30d, and miR-494 Regulate Human Endometrial Receptivity [J].
Altmaee, Signe ;
Martinez-Conejero, Jose A. ;
Esteban, Francisco J. ;
Ruiz-Alonso, Maria ;
Stavreus-Evers, Anneli ;
Horcajadas, Jose A. ;
Salumets, Andres .
REPRODUCTIVE SCIENCES, 2013, 20 (03) :308-317
[2]   Tumor suppressor genes on frequently deleted chromosome 3p in nasopharyngeal carcinoma [J].
Chen, Juan ;
Fu, Li ;
Zhang, Li-Yi ;
Kwong, Dora L. ;
Yan, Li ;
Guan, Xin-Yuan .
CHINESE JOURNAL OF CANCER, 2012, 31 (05) :215-222
[3]   Estrogen and ERα: Culprits in cervical cancer? [J].
Chung, Sang-Hyuk ;
Franceschi, Silvia ;
Lambert, Paul F. .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2010, 21 (08) :504-511
[4]   CHL1 COOPERATES WITH PAK1-3 TO REGULATE MORPHOLOGICAL DIFFERENTIATION OF EMBRYONIC CORTICAL NEURONS [J].
Demyanenko, G. P. ;
Halberstadt, A. I. ;
Rao, R. S. ;
Maness, P. F. .
NEUROSCIENCE, 2010, 165 (01) :107-115
[5]   Functional screening identifies miRNAs inducing cardiac regeneration [J].
Eulalio, Ana ;
Mano, Miguel ;
Dal Ferro, Matteo ;
Zentilin, Lorena ;
Sinagra, Gianfranco ;
Zacchigna, Serena ;
Giacca, Mauro .
NATURE, 2012, 492 (7429) :376-+
[6]   Role of microRNAs in Gynecological Pathology [J].
Gilabert-Estelles, J. ;
Braza-Boils, A. ;
Ramon, L. A. ;
Zorio, E. ;
Medina, P. ;
Espana, F. ;
Estelles, A. .
CURRENT MEDICINAL CHEMISTRY, 2012, 19 (15) :2406-2413
[7]  
Gocze K, 2013, ANTICANCER RES, V33, P2561
[8]   MicroRNA dysregulation in cancer: diagnostics, monitoring and therapeutics. A comprehensive review [J].
Iorio, Marilena V. ;
Croce, Carlo M. .
EMBO MOLECULAR MEDICINE, 2012, 4 (03) :143-159
[9]   MicroRNA-590-5p regulates proliferation and invasion in human hepatocellular carcinoma cells by targeting TGF-β RII [J].
Jiang, Xiaofeng ;
Xiang, Guangyang ;
Wang, Yezeng ;
Zhang, Lei ;
Yang, Xuewei ;
Cao, Liangqi ;
Peng, Heping ;
Xue, Ping ;
Chen, De .
MOLECULES AND CELLS, 2012, 33 (06) :545-551
[10]  
Khaliq SA, 2012, PAK J PHARM SCI, V25, P763