MicroRNAs in prostate cancer: from biomarkers to molecularly-based therapeutics

被引:33
作者
Gordanpour, A.
Nam, R. K. [2 ]
Sugar, L. [3 ]
Seth, A. [1 ,3 ]
机构
[1] Univ Toronto, Dept Lab Med & Pathobiol, Sunnybrook Res Inst, Toronto, ON M4N 3M5, Canada
[2] Sunnybrook Hlth Sci Ctr, Div Urol, Toronto, ON M4N 3M5, Canada
[3] Sunnybrook Hlth Sci Ctr, Dept Pathol, Toronto, ON M4N 3M5, Canada
关键词
microRNA; biomarker; therapeutics; TUMOR-SUPPRESSOR GENES; MESSENGER-RNAS; TARGETING MICRORNAS; DOWN-REGULATION; EXPRESSION; CELLS; TRANSLATION; METASTASIS; INVASION; GROWTH;
D O I
10.1038/pcan.2012.3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are effective regulators of gene expression that have a significant role in the pathogenesis of prostate and various other cancers. The high prevalence of aberrant miRNA expression in prostate cancer, and miRNAs' distinctive properties, give much hope that they can be used as biomarkers and next generation of molecular anticancer therapeutics. Herein, we review the literature on miRNA involvement in prostate cancer pathogenesis and the current understanding of their role as oncogenes, tumor suppressors and metastasis-regulators. We also review the latest research on miRNAs in prostate cancer preclinical studies and clinical trials, and highlight the advantages and challenges of possible miRNA-based therapies. The emerging information regarding the biology of miRNAs in prostate cancer is promising, and may lead to a role(s) for these molecules as diagnostic/prognostic markers and effective therapeutic tools for better molecularly targeted treatment of prostate cancer.
引用
收藏
页码:314 / 319
页数:6
相关论文
共 67 条
[1]   Genomic profiling of MicroRNA and messenger RNA reveals deregulated MicroRNA expression in prostate cancer [J].
Ambs, Stefan ;
Prueitt, Robyn L. ;
Yi, Ming ;
Hudson, Robert S. ;
Howe, Tiffany M. ;
Petrocca, Fabio ;
Wallace, Tiffany A. ;
Liu, Chang-Gong ;
Volinia, Stefano ;
Calin, George A. ;
Yfantis, Harris G. ;
Stephens, Robert M. ;
Croce, Carlo M. .
CANCER RESEARCH, 2008, 68 (15) :6162-6170
[2]   The Promise of MicroRNA Replacement Therapy [J].
Bader, Andreas G. ;
Brown, David ;
Winkler, Matthew .
CANCER RESEARCH, 2010, 70 (18) :7027-7030
[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]   The microRNA.org resource: targets and expression [J].
Betel, Doron ;
Wilson, Manda ;
Gabow, Aaron ;
Marks, Debora S. ;
Sander, Chris .
NUCLEIC ACIDS RESEARCH, 2008, 36 :D149-D153
[5]   The miR-15a-miR-16-1 cluster controls prostate cancer by targeting multiple oncogenic activities [J].
Bonci, Desiree ;
Coppola, Valeria ;
Musumeci, Maria ;
Addario, Antonio ;
Giuffrida, Raffaella ;
Memeo, Lorenzo ;
D'Urso, Leonardo ;
Pagliuca, Alfredo ;
Biffoni, Mauro ;
Labbaye, Catherine ;
Bartucci, Monica ;
Muto, Giovanni ;
Peschle, Cesare ;
De Maria, Ruggero .
NATURE MEDICINE, 2008, 14 (11) :1271-1277
[6]   Frequent deletions and down-regulation of micro-RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia [J].
Calin, GA ;
Dumitru, CD ;
Shimizu, M ;
Bichi, R ;
Zupo, S ;
Noch, E ;
Aldler, H ;
Rattan, S ;
Keating, M ;
Rai, K ;
Rassenti, L ;
Kipps, T ;
Negrini, M ;
Bullrich, F ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (24) :15524-15529
[7]   MicroRNAs modulate hematopoietic lineage differentiation [J].
Chen, CZ ;
Li, L ;
Lodish, HF ;
Bartel, DP .
SCIENCE, 2004, 303 (5654) :83-86
[8]   miR-148 targets human DNMT3b protein coding region [J].
Duursma, Anja M. ;
Kedde, Martijn ;
Schrier, Mariette ;
Le Sage, Carlos ;
Agami, Reuven .
RNA, 2008, 14 (05) :872-877
[9]   miR-331-3p Regulates ERBB-2 Expression and Androgen Receptor Signaling in Prostate Cancer [J].
Epis, Michael R. ;
Giles, Keith M. ;
Barker, Andrew ;
Kendrick, Tulene S. ;
Leedman, Peter J. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2009, 284 (37) :24696-24704
[10]   Most mammalian mRNAs are conserved targets of microRNAs [J].
Friedman, Robin C. ;
Farh, Kyle Kai-How ;
Burge, Christopher B. ;
Bartel, David P. .
GENOME RESEARCH, 2009, 19 (01) :92-105