MicroRNAs in clinical oncology: at the crossroads between promises and problems

被引:58
作者
Metias, S. M. [1 ,2 ]
Lianidou, E. [3 ]
Yousef, G. M. [1 ,2 ,4 ]
机构
[1] St Michaels Hosp, Dept Lab Med, Toronto, ON M5B 1W8, Canada
[2] St Michaels Hosp, Li Ka Shing Knowledge Inst, Keenan Res Ctr, Toronto, ON M5B 1W8, Canada
[3] Univ Athens, Fac Biol, Dept Biochem & Mol Biol, Athens, Greece
[4] Univ Toronto, Dept Lab Med & Pathobiol, Toronto, ON, Canada
关键词
CELL LUNG-CANCER; GENE-EXPRESSION; RNA INTERFERENCE; BREAST-CANCER; MIRNA; GROWTH; SIGNATURE; OVEREXPRESSION; DEREGULATION; INVOLVEMENT;
D O I
10.1136/jcp.2009.064717
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
MicroRNAs (miRNAs) are small RNAs that do not code for proteins, but function by controlling protein expression of other genes. miRNAs have been shown to control cell growth, differentiation and apoptosis. Shortly after their discovery, miRNAs have been found to be associated with cancer. Earlier reports have shown that human cancers frequently show a distorted expression profile of miRNAs. In this review, the biogenesis of miRNAs and potential mechanisms of their dysregulation and involvement in cancer pathogenesis are discussed. The current literature on potential applications of miRNAs in the field of clinical oncology from diagnostic to prognostic and predictive applications at the tissue, and more recently, serum levels, is reviewed. The potential therapeutic applications of miRNAs and RNAi in the field of cancer are summarised. Finally, some of the potential challenges that face the transition of miRNAs from a research setting into a clinical application are highlighted, with a future prospective of the incorporation of miRNAs in cancer patient management.
引用
收藏
页码:771 / 776
页数:6
相关论文
共 72 条
[51]   Microarray-based, high-throughput gene expression profiling of microRNAs [J].
Nelson, PT ;
Baldwin, DA ;
Scearce, LM ;
Oberholtzer, JC ;
Tobias, JW ;
Mourelatos, Z .
NATURE METHODS, 2004, 1 (02) :155-161
[52]   MicroRNA involvement in brain tumors: From bench to bedside [J].
Nicoloso, Milena S. ;
Calin, George A. .
BRAIN PATHOLOGY, 2008, 18 (01) :122-129
[53]   MicroRNA with a MacroFunction [J].
Rane, Shweta ;
Sayed, Danish ;
Abdellatif, Maha .
CELL CYCLE, 2007, 6 (15) :1850-1855
[54]  
Ross JS, 2007, AM J CLIN PATHOL, V128, P830, DOI 10.1309/2JK279BU2G743MWJ
[55]   Cancer-associated genomic regions (CAGRs) and noncoding RNAs: bioinformatics and therapeutic implications [J].
Rossi, Simona ;
Sevignani, Cinzia ;
Nnadi, Stephanie C. ;
Siracusa, Linda D. ;
Calin, George A. .
MAMMALIAN GENOME, 2008, 19 (7-8) :526-540
[56]   Regulation of microRNA processing in development, differentiation and cancer [J].
Schmittgen, Thomas D. .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2008, 12 (5B) :1811-1819
[57]   Coordinate suppression of ERBB2 and ERBB3 by enforced expression of micro-RNA miR-125a or miR-125b [J].
Scott, Gary K. ;
Goga, Andrei ;
Bhaumik, Dipa ;
Berger, Crystal E. ;
Sullivan, Christopher S. ;
Benz, Christopher C. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2007, 282 (02) :1479-1486
[58]   Targeting of microRNAs for therapeutics [J].
Stenvang, Jan ;
Lindow, Morten ;
Kauppinen, Sakari .
BIOCHEMICAL SOCIETY TRANSACTIONS, 2008, 36 :1197-1200
[59]   Micro-RNAs miR125b and miR137 are frequently upregulated in response to capecitabine chemoradiotherapy of rectal cancer [J].
Svoboda, M. ;
Holla, L. Izakovicova ;
Sefr, R. ;
Vrtkova, I. ;
Kocakova, I. ;
Tichy, B. ;
Dvorak, J. .
INTERNATIONAL JOURNAL OF ONCOLOGY, 2008, 33 (03) :541-547
[60]   Extensive post-transcriptional regulation of microRNAs and its implications for cancer [J].
Thomson, J. Michael ;
Newman, Martin ;
Parker, Joel S. ;
Morin-Kensicki, Elizabeth M. ;
Wright, Tricia ;
Hammond, Scott M. .
GENES & DEVELOPMENT, 2006, 20 (16) :2202-2207