Expression profile of microRNAs in c-Myc induced mouse mammary tumors

被引:67
作者
Sun, Yuan [1 ]
Wu, Jack [1 ,2 ]
Wu, Si-hung [1 ]
Thakur, Archana [2 ]
Bollig, Aliccia [2 ]
Huang, Yong [3 ]
Liao, D. Joshua [1 ]
机构
[1] Univ Minnesota, Hormel Inst, Austin, MN 55912 USA
[2] Wayne State Univ, Dept Pathol, Detroit, MI 48201 USA
[3] Univ Chicago, Dept Med, Med Genet Sect, Chicago, IL 60637 USA
关键词
c-myc; MicroRNA; Breast cancer; Microarray; SQUAMOUS-CELL CARCINOMA; X-CHROMOSOME; 13Q31-Q32; AMPLIFICATION; GENOMIC ALTERATIONS; POSSIBLE TARGET; LUNG CANCERS; GENE; IDENTIFICATION; SUSCEPTIBILITY; DELETION;
D O I
10.1007/s10549-008-0171-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
c-Myc is a transcription factor overexpression of which induces mammary cancer in transgenic mice. To explore whether certain microRNAs (mirRNA) mediate c-Myc induced mammary carcinogenesis, we studied mirRNA expression profile in mammary tumors developed from MMTV-c-myc transgenic mice, and found 50 and 59 mirRNAs showing increased and decreased expression, respectively, compared with lactating mammary glands of wild type mice. Twenty-four of these mirRNAs could be grouped into eight clusters because they had the same chromosomal localizations and might be processed from the same primary RNA transcripts. The increased expression of mir-20a, mir-20b, and mir-9 as well as decreased expression of mir-222 were verified by RT-PCR, real-timeRT-PCR, and cDNA sequencing. Moreover, we fortuitously identified a novel non-coding RNA, the level of which was decreased in proliferating mammary glands of MMTV-c-myc mice was further decreased to undetectable level in the mammary tumors. Sequencing of this novel RNA revealed that it was transcribed from a region of mouse chromosome 19 that harbored the metastasis associated lung adenocarcinoma transcript-1 (Malat-1), a non-protein-coding gene. These results suggest that certain mirRNAs and the chromosome 19 derived non-coding RNAs may mediate c-myc induced mammary carcinogenesis.
引用
收藏
页码:185 / 196
页数:12
相关论文
共 66 条
[1]   MicroRNAs - Future drug targets.? [J].
Arenz, Christoph .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2006, 45 (31) :5048-5050
[2]   Human microRNA genes are frequently located at fragile sites and genomic regions involved in cancers [J].
Calin, GA ;
Sevignani, C ;
Dan Dumitru, C ;
Hyslop, T ;
Noch, E ;
Yendamuri, S ;
Shimizu, M ;
Rattan, S ;
Bullrich, F ;
Negrini, M ;
Croce, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (09) :2999-3004
[3]   MicroRNA-cancer connection: The beginning of a new tale [J].
Calin, George Adrian ;
Croce, Carlo Maria .
CANCER RESEARCH, 2006, 66 (15) :7390-7394
[4]   Widespread microRNA repression by Myc contributes to tumorigenesis [J].
Chang, Tsung-Cheng ;
Yu, Duonan ;
Lee, Yun-Sil ;
Wentzel, Erik A. ;
Arking, Dan E. ;
West, Kristin M. ;
Dang, Chi V. ;
Thomas-Tikhonenko, Andrei ;
Mendell, Joshua T. .
NATURE GENETICS, 2008, 40 (01) :43-50
[5]   Identification of cancer/testis-antigen genes by massively parallel signature sequencing [J].
Chen, YT ;
Scanlan, MJ ;
Venditti, CA ;
Chua, R ;
Theiler, G ;
Stevenson, BJ ;
Iseli, C ;
Gure, AO ;
Vasicek, T ;
Strausberg, RL ;
Jongeneel, CV ;
Old, LJ ;
Simpson, AJG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (22) :7940-7945
[6]   Identification and characterization of mouse SSX genes:: a multigene family on the X chromosome with restricted cancer/testis expression [J].
Chen, YT ;
Alpen, B ;
Ono, T ;
Gure, AO ;
Scanlan, MA ;
Biggs, WH ;
Arden, K ;
Nakayama, E ;
Old, LJ .
GENOMICS, 2003, 82 (06) :628-636
[7]  
Choi C, 1997, GENE CHROMOSOME CANC, V20, P234
[8]  
Choi Chan, 1998, Journal of Korean Medical Science, V13, P311
[9]  
Chung HJ, 2005, MOL CELLS, V20, P157
[10]   The growing catalog of small RNAs and their association with distinct Argonaute/Piwi family members [J].
Farazi, Thalia A. ;
Juranek, Stefan A. ;
Tuschl, Thomas .
DEVELOPMENT, 2008, 135 (07) :1201-1214