Therapeutic MicroRNA Strategies in Human Cancer

被引:154
作者
Li, Chunsheng [1 ]
Feng, Yi [3 ]
Coukos, George [1 ,2 ,3 ]
Zhang, Lin [1 ,2 ]
机构
[1] Univ Penn, Sch Med, Ctr Res Early Detect & Cure Ovarian Canc, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Obstet & Gynecol, Philadelphia, PA 19104 USA
[3] Univ Penn, Sch Med, Abramson Family Canc Res Inst, Philadelphia, PA 19104 USA
来源
AAPS JOURNAL | 2009年 / 11卷 / 04期
关键词
cancer; microRNA; noncoding RNA; therapy; SMALL INTERFERING RNA; IN-VIVO; CELL-PROLIFERATION; REDUCED EXPRESSION; DOWN-REGULATION; SELF-RENEWAL; SOLID TUMORS; GENE; TARGET; LET-7;
D O I
10.1208/s12248-009-9145-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
MicroRNAs (miRNAs) are similar to 22 nucleotide long, noncoding, endogenous RNA molecules which exert their functions by base pairing with messenger RNAs (mRNAs), thereby regulate protein-coding gene expression. In eukaryotic cells, miRNAs play important roles in regulating biological processes such as proliferation, differentiation, apoptosis, and stem cell self-renewal. The human genome may contain as many as 1,000 miRNAs, and more than 700 of them have been identified. miRNAs are predicted to target up to one third of mRNAs. Each miRNA can target hundreds of transcripts directly or indirectly, while more than one miRNA can converge on a single transcript target. Therefore, the potential regulatory circuitry afforded by miRNA is enormous. Recently, mounting evidence implicates miRNAs as a new class of modulator for human tumor initiation and progression. Therefore, it has been proposed that manipulating miRNA activity and miRNA biogenesis may be a novel avenue for developing efficient therapies against cancer.
引用
收藏
页码:747 / 757
页数:11
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