Distinct roles for miR-1 and miR-133a in the proliferation and differentiation of rhabdomyosarcoma cells

被引:115
作者
Rao, Prakash K. [1 ]
Missiaglia, Edoardo [2 ]
Shields, Lauren [1 ,3 ]
Hyde, Greg [1 ]
Yuan, Bingbing [1 ]
Shepherd, Christopher J. [2 ]
Shipley, Janet [2 ]
Lodish, Harvey F. [1 ,3 ]
机构
[1] Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] Inst Canc Res, Mol Cytogenet Team, Sutton, Surrey, England
[3] MIT, Dept Biol, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
microRNA; muscle; tumor; MUSCLE-SPECIFIC MICRORNA; SKELETAL-MUSCLE; EXPRESSION SIGNATURE; GENE-EXPRESSION; IDENTIFICATION; TARGET; MYOGENESIS; INDUCE; MYOD;
D O I
10.1096/fj.09-150698
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Rhabdomyosarcoma is the most common soft tissue sarcoma in the pediatric population. As this tumor has an undifferentiated myogenic phenotype, agents that promote differentiation hold particular promise as part of a novel therapeutic approach to combat this type of cancer. In this report, we focus on the contribution of two microRNAs (miRNAs) in rhabdomyosarcomas. Levels of miR-1 and miR-133a are drastically reduced in representative cell lines from each major rhabdomyosarcoma subtype (embryonal and alveolar). Introduction of miR-1 and miR-133a into an embryonal rhabdomyosarcoma-derived cell line is cytostatic, thereby suggesting a tumor suppressor-like role for these myogenic miRNAs. Transcriptional profiling of cells after miR-1 and miR-133a expression reveals that miR-1 (but not miR-133a) exerts a strong promyogenic influence on these poorly differentiated tumor cells. We identify mRNAs that are down-regulated by these miRNAs and propose roles for miR-1 and miR-133a in repressing isoforms of genes that are normally not expressed in muscle. Finally, we show that mRNA targets of miR-1 and miR-133a are up-regulated in rhabdomyosarcomas, suggesting a causative role for these miRNAs in the development of rhabdomyosarcomas. More important, these results point to the promise of enhancing rhabdomyosarcoma therapy using miRNAs as agents that mediate cytostasis and promote muscle differentiation.-Rao, P. K., Missiaglia, E., Shields, L., Hyde, G., Yuan, B., Shepherd, C. J., Shipley, J., Lodish, H. F. Distinct roles for Mir-1 and Mir-133a in the proliferation and differentiation of rhabdomyosarcoma cells. FASEB J. 24, 3427-3437 (2010). www.fasebj.org
引用
收藏
页码:3427 / 3437
页数:11
相关论文
共 41 条
[1]  
Anderson J, 1999, GENE CHROMOSOME CANC, V26, P275, DOI 10.1002/(SICI)1098-2264(199912)26:4<275::AID-GCC1>3.3.CO
[2]  
2-V
[3]   MicroRNAs: Target Recognition and Regulatory Functions [J].
Bartel, David P. .
CELL, 2009, 136 (02) :215-233
[4]   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
[5]   Microarray profiling of microRNAs reveals frequent coexpression with neighboring miRNAs and host genes [J].
Baskerville, S ;
Bartel, DP .
RNA, 2005, 11 (03) :241-247
[6]   An initial blueprint for myogenic differentiation [J].
Blais, A ;
Tsikitis, M ;
Acosta-Alvear, D ;
Sharan, R ;
Kluger, Y ;
Dynlacht, BD .
GENES & DEVELOPMENT, 2005, 19 (05) :553-569
[7]   TPA-INDUCED DIFFERENTIATION OF HUMAN RHABDOMYOSARCOMA CELLS - EXPRESSION OF THE MYOGENIC REGULATORY FACTORS [J].
BOUCHE, M ;
SENNI, MI ;
GROSSI, AM ;
ZAPPELLI, F ;
POLIMENI, M ;
ARNOLD, HH ;
COSSU, G ;
MOLINARO, M .
EXPERIMENTAL CELL RESEARCH, 1993, 208 (01) :209-217
[8]   Identification of novel genes expressed during rhabdomyosarcoma differentiation using cDNA microarrays [J].
Carey, KA ;
Segal, D ;
Klein, R ;
Sanigorski, A ;
Walder, K ;
Collier, GR ;
Cameron-Smith, D .
PATHOLOGY INTERNATIONAL, 2006, 56 (05) :246-255
[9]   The role of microRNA-1 and microRNA-133 in skeletal muscle proliferation and differentiation [J].
Chen, JF ;
Mandel, EM ;
Thomson, JM ;
Wu, QL ;
Callis, TE ;
Hammond, SM ;
Conlon, FL ;
Wang, DZ .
NATURE GENETICS, 2006, 38 (02) :228-233
[10]   Identification of a PAX-FKHR gene expression signature that defines molecular classes and determines the prognosis of alveolar rhabdomyosarcomas [J].
Davicioni, Elai ;
Finckenstein, Friedrich Graf ;
Shahbazian, Violette ;
Buckley, Jonathan D. ;
Triche, Timothy J. ;
Anderson, Michael J. .
CANCER RESEARCH, 2006, 66 (14) :6936-6946