MicroRNA-139 suppresses proliferation in luminal type breast cancer cells by targeting Topoisomerase II alpha

被引:33
作者
Hua, Wei [1 ,2 ]
Sa, Ke-Di [2 ]
Zhang, Xiang [2 ]
Jia, Lin-Tao [2 ]
Zhao, Jing [2 ]
Yang, An-Gang [3 ]
Zhang, Rui [2 ]
Fan, Jing [4 ]
Bian, Ka [3 ,5 ]
机构
[1] Fourth Mil Med Univ, Xijing Hosp, Dept Obstet & Gynecol, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, State Key Lab Canc Biol, Dept Biochem & Mol Biol, Xian 710032, Peoples R China
[3] Fourth Mil Med Univ, Dept Immunol, State Key Lab Canc Biol, Xian 710032, Peoples R China
[4] Fourth Mil Med Univ, Xijing Hosp, Dept Vasc & Endocrine Surg, Xian 710032, Peoples R China
[5] Fourth Mil Med Univ, Tangdu Hosp, Dept Otolaryngol, Xian 710038, Peoples R China
基金
美国国家科学基金会;
关键词
microRNA; Breast cancer; Proliferation; TOP2a; METASTASIS; INVASION; SUBTYPES;
D O I
10.1016/j.bbrc.2015.06.061
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 classification of molecular subtypes of breast cancer improves the prognostic accuracy and therapeutic benefits in clinic. However, because of the complexity of breast cancer, more biomarkers and functional molecules need to be explored. Here, analyzing the data in a huge cohort of breast cancer patients, we found that Topoisomerase II alpha (TOP2a), an important target of chemotherapy is a biomarker for prognosis in luminal type breast cancer patients, but not in basal like or HERZ positive breast cancer patients. We identified that miR-139, a previous reported anti-metastatic microRNA targets 3'-untranslated region (3'UTR) of TOP2a mRNA. Further more, we revealed that the forced expression of miR-139 reduces the TOP2a expression at both mRNA and protein levels. And our functional experiments showed that the ectopic expression of miR-139 remarkably inhibits proliferation in luminal type breast cancer cells, while exogenous TOP2a expression could rescue inhibition of cell proliferation mediated by miR-139. Collectively, our present study demonstrates the miR-139-TOP2a regulatory axis is important for proliferation in luminal type breast cancer cells. This functional link may help us to further understand the specificity of subtypes of breast cancer and optimize the strategy of cancer treatment. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:1077 / 1083
页数:7
相关论文
共 28 条
[1]   miR-218 Suppresses Nasopharyngeal Cancer Progression through Downregulation of Survivin and the SLIT2-ROBO1 Pathway [J].
Alajez, Nehad M. ;
Lenarduzzi, Michelle ;
Ito, Emma ;
Hui, Angela B. Y. ;
Shi, Wei ;
Bruce, Jeff ;
Yue, Shijun ;
Huang, Shao H. ;
Xu, Wei ;
Waldron, John ;
O'Sullivan, Brian ;
Liu, Fei-Fei .
CANCER RESEARCH, 2011, 71 (06) :2381-2391
[2]   HER2 Interacts With CD44 to Up-regulate CXCR4 via Epigenetic Silencing of microRNA-139 in Gastric Cancer Cells [J].
Bao, Wei ;
Fu, Hai-Jing ;
Xie, Qiao-Sheng ;
Wang, Lei ;
Zhang, Rui ;
Guo, Zhang-Yan ;
Zhao, Jing ;
Meng, Yan-Ling ;
Ren, Xin-Ling ;
Wang, Tao ;
Li, Qing ;
Jin, Bo-Quan ;
Yao, Li-Bo ;
Wang, Rui-An ;
Fan, Dai-Ming ;
Chen, Si-Yi ;
Jia, Lin-Tao ;
Yang, An-Gang .
GASTROENTEROLOGY, 2011, 141 (06) :2076-U210
[3]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[4]   MicroRNA signatures highlight new breast cancer subtypes [J].
Bhattacharyya, Malay ;
Nath, Joyshree ;
Bandyopadhyay, Sanghamitra .
GENE, 2015, 556 (02) :192-198
[5]   Comparison of Breast Cancer Recurrence and Outcome Patterns Between Patients Treated From 1986 to 1992 and From 2004 to 2008 [J].
Cossetti, Rachel J. D. ;
Tyldesley, Scott K. ;
Speers, Caroline H. ;
Zheng, Yvonne ;
Gelmon, Karen A. .
JOURNAL OF CLINICAL ONCOLOGY, 2015, 33 (01) :65-U106
[6]   Molecular biology in breast cancer: Intrinsic subtypes and signaling pathways [J].
Eroles, Pilar ;
Bosch, Ana ;
Alejandro Perez-Fidalgo, J. ;
Lluch, Ana .
CANCER TREATMENT REVIEWS, 2012, 38 (06) :698-707
[7]   HER2 status and efficacy of adjuvant anthracyclines in early breast cancer:: A pooled analysis of randomized trials [J].
Gennari, Alessandra ;
Sormani, Maria Pia ;
Pronzato, Paolo ;
Puntoni, Matteo ;
Colozza, Mariantonietta ;
Pfeffer, Ulrich ;
Bruzzi, Paolo .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2008, 100 (01) :14-20
[8]   miRBase: tools for microRNA genomics [J].
Griffiths-Jones, Sam ;
Saini, Harpreet Kaur ;
van Dongen, Stijn ;
Enright, Anton J. .
NUCLEIC ACIDS RESEARCH, 2008, 36 :D154-D158
[9]   Molecular subclasses of breast cancer: how do we define them? The IMPAKT 2012 Working Group Statement [J].
Guiu, S. ;
Michiels, S. ;
Andre, F. ;
Cortes, J. ;
Denkert, C. ;
Di Leo, A. ;
Hennessy, B. T. ;
Sorlie, T. ;
Sotiriou, C. ;
Turner, N. ;
Van de Vijver, M. ;
Viale, G. ;
Loi, S. ;
Reis-Filho, J. S. .
ANNALS OF ONCOLOGY, 2012, 23 (12) :2997-3006
[10]   An online survival analysis tool to rapidly assess the effect of 22,277 genes on breast cancer prognosis using microarray data of 1,809 patients [J].
Gyoerffy, Balazs ;
Lanczky, Andras ;
Eklund, Aron C. ;
Denkert, Carsten ;
Budczies, Jan ;
Li, Qiyuan ;
Szallasi, Zoltan .
BREAST CANCER RESEARCH AND TREATMENT, 2010, 123 (03) :725-731