MicroRNAs and Metastasis: Little RNAs Go a Long Way

被引:179
作者
Dykxhoorn, Derek M. [1 ,2 ]
机构
[1] Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, John T Macdonald Fdn Dept Human Genet, Miami, FL 33136 USA
[2] Univ Miami, Miller Sch Med, John P Hussman Inst Human Genom, Dept Microbiol & Immunol, Miami, FL 33136 USA
关键词
EPITHELIAL-MESENCHYMAL TRANSITION; E-CADHERIN; CANCER METASTASIS; MIR-200; FAMILY; TUMOR; EXPRESSION; DISSEMINATION; COLONIZATION; MOVEMENT; INVASION;
D O I
10.1158/0008-5472.CAN-10-1346
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNA) are key regulators of many important biological processes from insulin secretion and fat metabolism to cellular proliferation and differentiation. Given the critical role that these small regulatory RNAs play in biology, it is not surprising that the alteration of miRNA expression patterns can have pathogenic consequences. The association between miRNA dysregulation and pathogenesis has been most widely studied in tumorigenesis, and a large number of miRNAs have been identified whose expression levels are changed in various tumor types. Although the role that miRNAs play in the development of metastasis is more poorly defined, recent studies have begun to identify miRNAs that can regulate key steps in the metastatic cascade. This review focuses on two emerging stories, the regulation of the epithelial-to-mesenchymal transition by members of the miR-200 family, and the pleiotropic nature of the metastasis suppressor miR-31. Cancer Res; 70(16); 6401-6. (C)2010 AACR.
引用
收藏
页码:6401 / 6406
页数:6
相关论文
共 26 条
[1]  
ASLAKSON CJ, 1992, CANCER RES, V52, P1399
[2]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[3]   Regulation of miR-200 family microRNAs and ZEB transcription factors in ovarian cancer: Evidence supporting a mesothelial-to-epithelial transition [J].
Bendoraite, Ausra ;
Knouf, Emily C. ;
Garg, Kavita S. ;
Parkin, Rachael K. ;
Kroh, Evan M. ;
O'Briant, Kathy C. ;
Ventura, Aviva P. ;
Godwin, Andrew K. ;
Karlan, Beth Y. ;
Drescher, Charles W. ;
Urban, Nicole ;
Knudsen, Beatrice S. ;
Tewari, Muneesh .
GYNECOLOGIC ONCOLOGY, 2010, 116 (01) :117-125
[4]   Causes and consequences of microRNA dysregulation in cancer [J].
Croce, Carlo M. .
NATURE REVIEWS GENETICS, 2009, 10 (10) :704-714
[5]   miR-200 Enhances Mouse Breast Cancer Cell Colonization to Form Distant Metastases [J].
Dykxhoorn, Derek M. ;
Wu, Yichao ;
Xie, Huangming ;
Yu, Fengyan ;
Lal, Ashish ;
Petrocca, Fabio ;
Martinvalet, Denis ;
Song, Erwei ;
Lim, Bing ;
Lieberman, Judy .
PLOS ONE, 2009, 4 (09)
[6]   Contextual extracellular cues promote tumor cell EMT and metastasis by regulating miR-200 family expression [J].
Gibbons, Don L. ;
Lin, Wei ;
Creighton, Chad J. ;
Rizvi, Zain H. ;
Gregory, Philip A. ;
Goodall, Gregory J. ;
Thilaganathan, Nishan ;
Du, Liqin ;
Zhang, Yiqun ;
Pertsemlidis, Alexander ;
Kurie, Jonathan M. .
GENES & DEVELOPMENT, 2009, 23 (18) :2140-2151
[7]   MicroRNAs as regulators of epithelial-mesenchymal transition [J].
Gregory, Philip. A. ;
Bracken, Cameron P. ;
Bert, Andrew G. ;
Goodall, Gregory J. .
CELL CYCLE, 2008, 7 (20) :3112-3117
[8]   The mir-200 family and mir-205 regulate epithelial to mesenchymal transition by targeting ZEB1 and SIP1 [J].
Gregory, Philip A. ;
Bert, Andrew G. ;
Paterson, Emily L. ;
Barry, Simon C. ;
Tsykin, Anna ;
Farshid, Gelareh ;
Vadas, Mathew A. ;
Khew-Goodall, Yeesim ;
Goodall, Gregory J. .
NATURE CELL BIOLOGY, 2008, 10 (05) :593-601
[9]   Metastamir: The Field of Metastasis-Regulatory microRNA Is Spreading [J].
Hurst, Douglas R. ;
Edmonds, Mich D. ;
Welch, Danny R. .
CANCER RESEARCH, 2009, 69 (19) :7495-7498
[10]   Stable expression of miR-200c alone is sufficient to regulate TCF8 (ZEB1) and restore E-cadherin expression [J].
Hurteau, Gregory J. ;
Carlson, J. Andrew ;
Roos, Eric ;
Brock, Graham J. .
CELL CYCLE, 2009, 8 (13) :2064-2069