MicroRNA-21 in breast cancer: diagnostic and prognostic potential

被引:56
作者
Chen, J. [1 ]
Wang, X. [1 ]
机构
[1] Zhejiang Canc Hosp, Dept Med Oncol Breast, Hangzhou 310022, Zhejiang, Peoples R China
关键词
MicroRNA-21; Breast cancer; Biomarker; Diagnosis; Prognosis; CIRCULATING MICRORNAS; CLINICAL-SIGNIFICANCE; MIR-21; EXPRESSION; GENE-EXPRESSION; BIOMARKERS; SERUM; IDENTIFICATION; MARKERS; TARGETS; OVEREXPRESSION;
D O I
10.1007/s12094-013-1132-z
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer is the most common malignancy in women and is considered as a complex and heterogeneous disease. The identification of novel biomarkers for early detection of breast cancer and prediction of disease outcome is urgently required. MicroRNAs (miRNAs) are small non-coding endogenous RNA molecules that act to regulate gene expression and play vital roles in many crucial processes. Recent evidence demonstrates that miRNAs could emerge as revolutionary sources of biomarkers for cancer diagnosis and prognosis. miR-21 is one of the most commonly observed aberrant miRNAs in a variety of cancers including breast cancer. Emerging studies show that miR-21 could be measured stably and easily in tumor tissues, formalin-fixed paraffin-embedded tissues and blood circulation. In this review, we will summarize the current evidence of miR-21 as a promising biomarker for diagnosis and prognosis in breast cancer. We will also discuss the issues and challenges of miR-21 as a potential biomarker in future clinical applications.
引用
收藏
页码:225 / 233
页数:9
相关论文
共 60 条
[1]   Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma [J].
Arroyo, Jason D. ;
Chevillet, John R. ;
Kroh, Evan M. ;
Ruf, Ingrid K. ;
Pritchard, Colin C. ;
Gibson, Donald F. ;
Mitchell, Patrick S. ;
Bennett, Christopher F. ;
Pogosova-Agadjanyan, Era L. ;
Stirewalt, Derek L. ;
Tait, Jonathan F. ;
Tewari, Muneesh .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (12) :5003-5008
[2]   Direct Serum Assay for MicroRNA-21 Concentrations in Early and Advanced Breast Cancer [J].
Asaga, Sota ;
Kuo, Christine ;
Nguyen, Tung ;
Terpenning, Marilou ;
Giuliano, Armando E. ;
Hoon, Dave S. B. .
CLINICAL CHEMISTRY, 2011, 57 (01) :84-91
[3]   MicroRNAs: Genomics, biogenesis, mechanism, and function (Reprinted from Cell, vol 116, pg 281-297, 2004) [J].
Bartel, David P. .
CELL, 2007, 131 (04) :11-29
[4]   Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers [J].
Calin, GA ;
Sevignani, C ;
Dan Dumitru, C ;
Hyslop, T ;
Noch, E ;
Yendamuri, S ;
Shimizu, M ;
Rattan, S ;
Bullrich, F ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :2999-3004
[5]   hsa-miR-210 is induced by hypoxia and is an independent prognostic factor in breast cancer [J].
Camps, Carme ;
Buffa, Francesca M. ;
Colella, Stefano ;
Moore, John ;
Sotiriou, Christos ;
Sheldon, Helen ;
Harris, Adrian L. ;
Gleadle, Jonathan M. ;
Ragoussis, Jiannis .
CLINICAL CANCER RESEARCH, 2008, 14 (05) :1340-1348
[6]   MicroRNA-21 is an antiapoptotic factor in human glioblastoma cells [J].
Chan, JA ;
Krichevsky, AM ;
Kosik, KS .
CANCER RESEARCH, 2005, 65 (14) :6029-6033
[7]   Role of Deregulated microRNAs in Breast Cancer Progression Using FFPE Tissue [J].
Chen, Liang ;
Li, Youhuai ;
Fu, Yebo ;
Peng, Jin ;
Mo, Meng-Hsuan ;
Stamatakos, Michael ;
Teal, Christine B. ;
Brem, Rachel F. ;
Stojadinovic, Alexander ;
Grinkemeyer, Michael ;
McCaffrey, Timothy A. ;
Man, Yan-Gao ;
Fu, Sidney W. .
PLOS ONE, 2013, 8 (01)
[8]   Characterization of microRNAs in serum: a novel class of biomarkers for diagnosis of cancer and other diseases [J].
Chen, Xi ;
Ba, Yi ;
Ma, Lijia ;
Cai, Xing ;
Yin, Yuan ;
Wang, Kehui ;
Guo, Jigang ;
Zhang, Yujing ;
Chen, Jiangning ;
Guo, Xing ;
Li, Qibin ;
Li, Xiaoying ;
Wang, Wenjing ;
Zhang, Yan ;
Wang, Jin ;
Jiang, Xueyuan ;
Xiang, Yang ;
Xu, Chen ;
Zheng, Pingping ;
Zhang, Juanbin ;
Li, Ruiqiang ;
Zhang, Hongjie ;
Shang, Xiaobin ;
Gong, Ting ;
Ning, Guang ;
Wang, Jun ;
Zen, Ke ;
Zhang, Junfeng ;
Zhang, Chen-Yu .
CELL RESEARCH, 2008, 18 (10) :997-1006
[9]  
Cheng HR, 2013, PLOS ONE, V8, DOI [10.1371/journal.pone.0064795, 10.1371/journal.pone.0053008]
[10]   Programmed cell death 4 (PDCD4) is an important functional target of the microRNA miR-21 in breast cancer cells [J].
Frankel, Lisa B. ;
Christoffersen, Nanna R. ;
Jacobsen, Anders ;
Lindow, Morten ;
Krogh, Anders ;
Lund, Anders H. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (02) :1026-1033