MicroRNA-145 Targets YES and STAT1 in Colon Cancer Cells

被引:140
作者
Gregersen, Lea H. [1 ,2 ,3 ]
Jacobsen, Anders B. [3 ]
Frankel, Lisa B. [1 ,2 ]
Wen, Jiayu [3 ]
Krogh, Anders [1 ,2 ,3 ]
Lund, Anders H. [1 ,2 ]
机构
[1] Univ Copenhagen, Biotech Res & Innovat Ctr, Copenhagen, Denmark
[2] Univ Copenhagen, Ctr Epigenet, Copenhagen, Denmark
[3] Univ Copenhagen, Dept Biol, Bioinformat Ctr, Copenhagen, Denmark
来源
PLOS ONE | 2010年 / 5卷 / 01期
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
SUPPRESSIVE MICRORNAS; COLORECTAL-CANCER; EXPRESSION; GROWTH; SIGNATURES; MECHANISM; MIR-143; IDENTIFICATION; DETERMINANTS; DEREGULATION;
D O I
10.1371/journal.pone.0008836
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: MicroRNAs (miRNAs) have emerged as important gene regulators and are recognized as key players in tumorigenesis. miR-145 is reported to be down-regulated in several cancers, but knowledge of its targets in colon cancer remains limited. Methodology/Principal Findings: To investigate the role of miR-145 in colon cancer, we have employed a microarray based approach to identify miR-145 targets. Based on seed site enrichment analyses and unbiased word analyses, we found a significant enrichment of miRNA binding sites in the 3'-untranslated regions (UTRs) of transcripts down-regulated upon miRNA overexpression. Gene Ontology analysis showed an overrepresentation of genes involved in cell death, cellular growth and proliferation, cell cycle, gene expression and cancer. A number of the identified miRNA targets have previously been implicated in cancer, including YES, FSCN1, ADAM17, BIRC2, VANGL1 as well as the transcription factor STAT1. Both YES and STAT1 were verified as direct miR-145 targets. Conclusions/Significance: The study identifies and validates new cancer-relevant direct targets of miR-145 in colon cancer cells and hereby adds important mechanistic understanding of the tumor-suppressive functions of miR-145.
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页数:10
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