Identification of let-7-regulated oncofetal genes

被引:177
作者
Boyerinas, Benjamin [1 ]
Park, Sun-Mi [1 ]
Shomron, Noam [2 ]
Hedegaard, Mads M. [3 ]
Vinther, Jeppe [3 ]
Andersen, Jens S. [3 ,4 ]
Feig, Christine [1 ]
Xu, Jinbo [5 ]
Burg, Christopher B. [2 ]
Peter, Marcus E. [1 ]
机构
[1] Univ Chicago, Ben May Dept Canc Res, Chicago, IL 60637 USA
[2] MIT, Dept Biol, Cambridge, MA USA
[3] Univ Copenhagen, Inst Mol Biol, Mol Evolut Grp, Copenhagen, Denmark
[4] Univ So Denmark, Dept Biochem & Mol Biol, Ctr Expt Bioinformat, Odense, Denmark
[5] Toyota Technol Inst, Chicago, IL USA
关键词
D O I
10.1158/0008-5472.CAN-08-0264
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNA) are small RNA molecules of similar to 20 to 22 nucleotides that reduce expression of proteins through mRNA degradation and/or translational silencing. Each known miRNA has a large number of predicted targets. Members of the let-7/miR-98 family of miRNAs are up-regulated at the end of embryonic development. Let-7 is often down-regulated early during cancer development, suggesting that let-7-regulated oncofetal genes (LOG) may become reexpressed in cancer cells. Using comparative bioinformatics, we have identified 12 conserved LOGs that include HMGA2 and IMP-1/CRD-BP. IMP-1 has growth-promoting activities through stabilization of c-myc mRNA. We experimentally confirmed that IMP-1 is a direct let-7 target that promotes cell growth and motility of tumor cells, and we confirmed by proteomics analysis that IMP-1 and HMGA2 are major miRNA targets. Our data suggest that a substantial part of the growth inhibitory activities of let-7 comes from suppressing the expression of IMP-1. LOGs could be novel therapeutic targets and potential biomarkers for cancer treatment.
引用
收藏
页码:2587 / 2591
页数:5
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