The role of let-7 in cell differentiation and cancer

被引:562
作者
Boyerinas, Benjamin [1 ]
Park, Sun-Mi [1 ]
Hau, Annika [1 ]
Murmann, Andrea E. [1 ]
Peter, Marcus E. [1 ]
机构
[1] Univ Chicago, Ben May Dept Canc Res, Chicago, IL 60637 USA
关键词
MICRORNA EXPRESSION PROFILES; BINDING-SITE POLYMORPHISM; 3' UNTRANSLATED REGION; BREAST-CANCER; OVARIAN-CANCER; DOWN-REGULATION; POSTTRANSCRIPTIONAL REGULATION; SELECTIVE BLOCKADE; RNA-INTERFERENCE; MESSENGER-RNA;
D O I
10.1677/ERC-09-0184
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs or miRs) are small noncoding RNAs capable of regulating gene expression at the translational level. Current evidence suggests that a significant portion of the human genome is regulated by microRNAs, and many reports have demonstrated that microRNA expression is deregulated in human cancer. The let-7 family of microRNAs, first discovered in Caenorhabditis elegans, is functionally conserved from worms to humans. The human let-7 family contains 13 members located on nine different chromosomes, and many human cancers have deregulated let-7 expression. A growing body of evidence suggests that restoration of let-7 expression may be a useful therapeutic option in cancers, where its expression has been lost. In this review, we discuss the role of let-7 in normal development and differentiation, and provide an overview of the relationship between deregulated let-7 expression and tumorigenesis. The regulation of let-7 expression, cancer-relevant let-7 targets, and the relationship between let-7 and drug sensitivity are highlighted.
引用
收藏
页码:F19 / F36
页数:18
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