MicroRNA-185 inhibits proliferation by targeting c-Met in human breast cancer cells

被引:35
作者
Fu, Peifen [1 ]
Du, Feiya [2 ]
Yao, Minya [1 ]
Lv, Kezhen [1 ]
Liu, Yu [1 ]
机构
[1] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Dept Breast Surg, Hangzhou 310003, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Affiliated Hosp 1, Dept Plast Surg, Hangzhou 310003, Zhejiang, Peoples R China
关键词
breast cancer; cell proliferation; miR-I85; c-Met; RESISTANCE; KINASE; RECOGNITION; EXPRESSION; APOPTOSIS; BINDING; GENES;
D O I
10.3892/etm.2014.1999
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
MicroRNAs (miRNAs) are a group of small non-coding RNA molecules that have been shown to regulate the expression of genes involved in tumorigenesis. The relevance of miRNAs in the development, progression and prognosis of human breast cancer is not fully understood. miR-185 has been demonstrated to be involved in the pathogenesis of several types of cancers; however, its role in breast cancer has not yet been elucidated. In the present study, the expression of miR-185 was analyzed by quantitative polymerase chain reaction. In addition, an MTT assay and flow cytometry were used to determine the rates of cell proliferation and apoptosis. Protein expression was analyzed by western blotting and the target gene was confirmed using a luciferase reporter assay. The expression of miR-185 was found to be downregulated in the breast cancer tissues. The MTT assay revealed that overexpression of miR-185 inhibited the proliferation of MDF7 and SKBR3 cells. Furthermore, flow cytometric analysis demonstrated that increased expression levels of miR-185 promoted the apoptosis of breast cancer cells. In addition, c-Met expression was demonstrated to be significantly upregulated in breast cancer tissues and cells, and the c-Met gene was identified to be a target of miR-185. Therefore, the results demonstrated that miR-185 inhibited the proliferation of breast cancer cells by regulating the expression of c-Met, indicating its potential as a therapeutic target for breast cancer.
引用
收藏
页码:1879 / 1883
页数:5
相关论文
共 24 条
[1]   Comparisons between different polychemotherapy regimens for early breast cancer: meta-analyses of long-term outcome among 100 000 women in 123 randomised trials [J].
Albain, K. ;
Anderson, S. ;
Arriagada, R. ;
Barlow, W. ;
Bergh, J. ;
Bliss, J. ;
Buyse, M. ;
Cameron, D. ;
Carrasco, E. ;
Clarke, M. ;
Correa, C. ;
Coates, A. ;
Collins, R. ;
Costantino, J. ;
Cutter, D. ;
Cuzick, J. ;
Darby, S. ;
Davidson, N. ;
Davies, C. ;
Davies, K. ;
Delmestri, A. ;
Di Leo, A. ;
Dowsett, M. ;
Elphinstone, P. ;
Evans, V. ;
Ewertz, M. ;
Gelber, R. ;
Gettins, L. ;
Geyer, C. ;
Goldhirsch, A. ;
Godwin, J. ;
Gray, R. ;
Gregory, C. ;
Hayes, D. ;
Hill, C. ;
Ingle, J. ;
Jakesz, R. ;
James, S. ;
Kaufmann, M. ;
Kerr, A. ;
MacKinnon, E. ;
McGale, P. ;
McHugh, T. ;
Norton, L. ;
Ohashi, Y. ;
Paik, S. ;
Pan, H. C. ;
Perez, E. ;
Peto, R. ;
Piccart, M. .
LANCET, 2012, 379 (9814) :432-444
[2]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[3]   miR-15 and miR-16 induce apoptosis by targeting BCL2 [J].
Cimmino, A ;
Calin, GA ;
Fabbri, M ;
Iorio, MV ;
Ferracin, M ;
Shimizu, M ;
Wojcik, SE ;
Aqeilan, RI ;
Zupo, S ;
Dono, M ;
Rassenti, L ;
Alder, H ;
Volinia, S ;
Liu, CG ;
Kipps, TJ ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (39) :13944-13949
[4]   Causes and consequences of microRNA dysregulation in cancer [J].
Croce, Carlo M. .
NATURE REVIEWS GENETICS, 2009, 10 (10) :704-714
[5]   Breast Cancer Statistics, 2013 [J].
DeSantis, Carol ;
Ma, Jiemin ;
Bryan, Leah ;
Jemal, Ahmedin .
CA-A CANCER JOURNAL FOR CLINICIANS, 2014, 64 (01) :52-62
[6]   Roles of microRNAs during prostatic tumorigenesis and tumor progression [J].
Fang, Y-X ;
Gao, W-Q .
ONCOGENE, 2014, 33 (02) :135-147
[7]  
Higgs Gadareth, 2013, J Clin Bioinforma, V3, P17, DOI 10.1186/2043-9113-3-17
[8]   miR-24 Inhibits Cell Proliferation by Targeting E2F2, MYC, and Other Cell-Cycle Genes via Binding to "Seedless" 3′UTR MicroRNA Recognition Elements [J].
Lal, Ashish ;
Navarro, Francisco ;
Maher, Christopher A. ;
Maliszewski, Laura E. ;
Yan, Nan ;
O'Day, Elizabeth ;
Chowdhury, Dipanjan ;
Dykxhoorn, Derek M. ;
Tsai, Perry ;
Hofmann, Oliver ;
Becker, Kevin G. ;
Gorospe, Myriam ;
Hide, Winston ;
Lieberman, Judy .
MOLECULAR CELL, 2009, 35 (05) :610-625
[9]   c-Met Is a Marker of Pancreatic Cancer Stem Cells and Therapeutic Target [J].
Li, Chenwei ;
Wu, Jing-Jiang ;
Hynes, Mark ;
Dosch, Joseph ;
Sarkar, Bedabrata ;
Welling, Theodore H. ;
di Magliano, Marina Pasca ;
Simeone, Diane M. .
GASTROENTEROLOGY, 2011, 141 (06) :2218-U395
[10]   miR-185 targets RhoA and Cdc42 expression and inhibits the proliferation potential of human colorectal cells [J].
Liu, Ming ;
Lang, Nan ;
Chen, Xiangzhen ;
Tang, Qiulin ;
Liu, Surui ;
Huang, Juan ;
Zheng, Yi ;
Bi, Feng .
CANCER LETTERS, 2011, 301 (02) :151-160