MicroRNA in Prostate, Bladder, and Kidney Cancer: A Systematic Review

被引:388
作者
Catto, James W. F. [1 ,2 ]
Alcaraz, Antonio [3 ]
Bjartell, Anders S. [4 ]
White, Ralph De Vere [5 ]
Evans, Christopher P. [5 ]
Fussel, Susanne [6 ]
Hamdy, Freddie C. [7 ]
Kallioniemi, Olli [8 ]
Mengual, Lourdes [3 ]
Schlomm, Thorsten [9 ]
Visakorpi, Tapio [10 ,11 ]
机构
[1] Univ Sheffield, Sch Med, Inst Canc Studies, Sheffield S10 2RX, S Yorkshire, England
[2] Univ Sheffield, Acad Urol Unit, Sheffield S10 2RX, S Yorkshire, England
[3] Univ Barcelona, Dept & Lab Urol, Hosp Clin, IDIBAPS, E-08036 Barcelona, Spain
[4] Skane Univ Hosp, Dept Urol, Malmo, Sweden
[5] Univ Calif Davis, Dept Urol, Sch Med, Sacramento, CA 95817 USA
[6] Tech Univ Dresden, Dept Urol, Dresden, Germany
[7] Univ Oxford, Nuffield Dept Surg, Oxford, England
[8] Univ Helsinki, Inst Mol Med Finland FIMM, Nord EMBL Partnership Mol Med, Helsinki, Finland
[9] Univ Med Ctr, Prostate Canc Ctr, Hamburg, Germany
[10] Univ Tampere, Inst Med Technol, FIN-33101 Tampere, Finland
[11] Tampere Univ Hosp, Tampere, Finland
关键词
MicroRNA; Gene regulation; Prostate; Bladder; Kidney; Cancer; ATTENUATES PACLITAXEL-RESISTANCE; PUTATIVE TUMOR-SUPPRESSOR; RENAL-CELL CARCINOMA; MESSENGER-RNA; DEPENDENT REGULATION; DOWN-REGULATION; PC3; CELLS; EXPRESSION; GROWTH; OVEREXPRESSION;
D O I
10.1016/j.eururo.2011.01.044
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Context: MicroRNAs (miRNA) are noncoding RNAs that post- transcriptionally regulate gene expression. Their altered expression and function have been observed in most urologic cancers. MiRNAs represent potential disease biomarkers and novel therapeutic targets. Objective: To review and evaluate the evidence implicating miRNAs in the pathogenesis of prostate cancer (PCa), bladder cancer (BCa), and renal cancer. Evidence acquisition: A systematic review was performed using PubMed and Embase to search for reports using strings for microRNA, non- coding RNA, cancer, prostate, bladder, and renal cancer. Identified manuscripts were retrieved and references searched. Selected studies were required to concentrate on the role of miRNA in these urologic cancers. Evidence synthesis: We reviewed articles that focus on this topic. More than 40 miRNAs have been implicated in urologic cancer and many target common carcinogenic pathways. In particular, apoptosis avoidance, cell proliferation, epithelial- to- mesenchymal transition, angiogenic signalling, and the generation of androgen independence are targeted or facilitated by more than one miRNA. Little work has been done to evaluate the translational applications for this knowledge to date. Novel therapeutic strategies have been developed and are under investigation to selectively modulate miRNAs; such work would potentially enable personalised tumour therapy. Conclusions: MiRNAs appear to be important modulators of urologic cancer. Their expression is frequently altered in these tumours, and many are functionally implicated in their pathogenesis. They require evaluation to determine the translational role and therapeutic potential for this knowledge. Crown Copyright (C) 2011 Published by Elsevier B. V. on behalf of European Association of Urology. All rights reserved.
引用
收藏
页码:671 / 681
页数:11
相关论文
共 96 条
[1]   miR-200 Expression Regulates Epithelial-to-Mesenchymal Transition in Bladder Cancer Cells and Reverses Resistance to Epidermal Growth Factor Receptor Therapy [J].
Adam, Liana ;
Zhong, Meng ;
Choi, Woonyoung ;
Qi, Wei ;
Nicoloso, Milena ;
Arora, Ameeta ;
Calin, George ;
Wang, Hua ;
Siefker-Radtke, Arlene ;
McConkey, David ;
Bar-Eli, Menashe ;
Dinney, Colin .
CLINICAL CANCER RESEARCH, 2009, 15 (16) :5060-5072
[2]   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
[3]   The Promise of MicroRNA Replacement Therapy [J].
Bader, Andreas G. ;
Brown, David ;
Winkler, Matthew .
CANCER RESEARCH, 2010, 70 (18) :7027-7030
[4]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[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]   Circulating miRNAs are correlated with tumor progression in prostate cancer [J].
Brase, Jan C. ;
Johannes, Marc ;
Schlomm, Thorsten ;
Faelth, Maria ;
Haese, Alexander ;
Steuber, Thomas ;
Beissbarth, Tim ;
Kuner, Ruprecht ;
Sueltmann, Holger .
INTERNATIONAL JOURNAL OF CANCER, 2011, 128 (03) :608-616
[7]   RNA Interference Advances to Early-Stage Clinical Trials [J].
Brower, Vicki .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2010, 102 (19) :1459-1461
[8]   A reciprocal repression between ZEB1 and members of the miR-200 family promotes EMT and invasion in cancer cells [J].
Burk, Ulrike ;
Schubert, Joerg ;
Wellner, Ulrich ;
Schmalhofer, Otto ;
Vincan, Elizabeth ;
Spaderna, Simone ;
Brabletz, Thomas .
EMBO REPORTS, 2008, 9 (06) :582-589
[9]   A MicroRNA signature associated with prognosis and progression in chronic lymphocytic leukemia [J].
Calin, GA ;
Ferracin, M ;
Cimmino, A ;
Di Leva, G ;
Shimizu, M ;
Wojcik, SE ;
Iorio, MV ;
Visone, R ;
Sever, NI ;
Fabbri, M ;
Iuliano, R ;
Palumbo, T ;
Pichiorri, F ;
Roldo, C ;
Garzon, R ;
Sevignani, C ;
Rassenti, L ;
Alder, H ;
Volinia, S ;
Liu, CG ;
Kipps, TJ ;
Negrini, M ;
Croce, CM .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (17) :1793-1801
[10]   MicroRNA profiling reveals distinct signatures in B cell chronic lymphocytic leukemias [J].
Calin, GA ;
Liu, CG ;
Sevignani, C ;
Ferracin, M ;
Felli, N ;
Dumitru, CD ;
Shimizu, M ;
Cimmino, A ;
Zupo, S ;
Dono, M ;
Dell'Aquila, ML ;
Alder, H ;
Rassenti, L ;
Kipps, TJ ;
Bullrich, F ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (32) :11755-11760