MicroRNAs and genomic variations: from Proteus tricks to Prometheus gift

被引:23
作者
Fabbri, Muller [1 ]
Valeri, Nicola [1 ]
Calin, George A. [2 ]
机构
[1] Ohio State Univ, Ctr Comprehens Canc, Dept Mol Virol Immunol & Med Genet, Columbus, OH 43210 USA
[2] Univ Texas MD Anderson Canc Ctr, Dept Expt Therapeut & Canc Genet, Houston, TX 77030 USA
关键词
SINGLE-NUCLEOTIDE POLYMORPHISM; DIHYDROFOLATE-REDUCTASE GENE; PAPILLARY THYROID-CARCINOMA; BINDING-SITES; BREAST-CANCER; FUNCTIONAL POLYMORPHISM; MIR-146A GENE; TARGET SITES; EXPRESSION; RISK;
D O I
10.1093/carcin/bgp063
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are small non-coding RNAs with regulatory functions. MiRNAs are aberrantly expressed in almost all human cancers, leading to abnormal levels of target genes. Recently, an increasing number of studies have addressed whether genomic variations including germ line or somatic mutations and single-nucleotide polymorphisms can count for miRNA abnormal expression by altering their biogenesis and/or affect the ability of miRNAs to bind to target messenger RNAs. Here, we provide an extensive review of the studies that have investigated variations occurring both in miRNA genes and in target genes and we discuss the possible clinical implications of these findings. Furthermore, we propose that sequence variations in miRNAs or interactor sites located in mRNAs can be involved in cancer predisposition.
引用
收藏
页码:912 / 917
页数:6
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