MiR-15a, miR-16-1 and miR-17-92 cluster expression are linked to poor prognosis in multiple myeloma

被引:68
作者
Gao, Xiao [1 ]
Zhang, Run [1 ]
Qu, Xiaoyan [1 ]
Zhao, Min [1 ]
Zhang, Sensen [1 ]
Wu, Hanxin [1 ]
Li Jianyong [1 ]
Chen, Lijuan [1 ]
机构
[1] Nanjing Med Univ, Dept Hematol, Affiliated Hosp 1, Jiangsu Prov Hosp, Nanjing 210029, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
MiR-15a; MiR-16-1; MiR-17-92; cluster; del(13); Multiple myeloma; MICRORNA EXPRESSION; IN-SITU; STAGING SYSTEM; ABNORMALITIES; SIGNATURES; DEREGULATION; DELETION; 13Q14; RNA;
D O I
10.1016/j.leukres.2012.08.021
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multiple myeloma (MM) is characterized by a profound genomic instability of potential prognostic relevance. Loss of chromosome 13, observed in almost half of patients, negatively affects prognosis. MiR-15a, miR16-1 and miR-17-92 cluster, located on 13q, play important roles in the regulation of cell proliferation, differentiation and apoptosis. Therefore, we investigated a possible correlation of miRNA expression with chromosome 13 deletions (del(13)) and prognosis. We measured the expression of miR-15a, miR16-1 in 70 newly diagnosed MM patients and miR-17-92 cluster in 85 newly diagnosed MM patients by quantitative real-time PCR analyses. MiR-15a, miR-16-1 and miR-17-92 cluster expression levels are independent of the del(13). High levels of miR-15a, miR-16-1, miR-17, miR-20a and miR-92-1 are associated with shorter progression-free survival (PFS), suggesting poor prognosis. Our data suggest that the expression of specific miRNAs may be contributing to MM prognosis. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1505 / 1509
页数:5
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