Role of miR-15/16 in CLL

被引:152
作者
Pekarsky, Y. [1 ]
Croce, C. M. [1 ]
机构
[1] Wexner Med Ctr, Dept Mol Virol Immunol & Med Genet, Columbus, OH USA
关键词
CHRONIC LYMPHOCYTIC-LEUKEMIA; DOWN-REGULATION; INDUCE APOPTOSIS; B-CELLS; 13Q14; BCL-2; GENE; EXPRESSION; PROLIFERATION; SEQUENCE;
D O I
10.1038/cdd.2014.87
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
B-cell chronic lymphocytic leukemia (CLL) is the most common adult leukemia. The most common chromosomal abnormalities detectable by cytogenetics include deletion at 13q (55%), 11q (18%), trisomy 12 (12-16%) and 17p (8%). In 2002, we discovered that a microRNA cluster miR-15a/miR-16-1 (miR-15/16) is the target of 13q deletions in CLL. MicroRNAs encoded by the miR-15/16 locus (miR-15 and miR-16) function as tumor suppressors. Expression of these miRNAs downregulated in CLL, melanoma, colorectal cancer, bladder cancer and other solid tumors. miR-15/16 cluster targets multiple oncogenes, including BCL2, Cyclin D1, MCL1 and others. The most important target of miR-15/16 in CLL is arguably BCL2, as BCL2 is overexpressed in almost all CLLs. In this review, we discuss the discovery, functions, clinical relevance and treatment opportunities related to miR-15/16.
引用
收藏
页码:6 / 11
页数:6
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