MicroRNA expression in tumor cells from Waldenstrom's macroglobulinemia reflects both their normal and malignant cell counterparts

被引:16
作者
Hodge, L. S. [1 ]
Elsawa, S. F. [1 ]
Grote, D. M. [1 ]
Price-Troska, T. L. [1 ]
Asmann, Y. W. [2 ]
Fonseca, R. [3 ]
Gertz, M. A. [1 ]
Witzig, T. E. [1 ]
Novak, A. J. [1 ]
Ansell, S. M. [1 ]
机构
[1] Mayo Clin, Div Hematol & Internal Med, Rochester, MN 55905 USA
[2] Mayo Clin, Div Biomed Informat, Rochester, MN 55905 USA
[3] Mayo Clin, Ctr Comprehens Canc, Scottsdale, AZ USA
关键词
microRNA; Waldenstrom's macroglobulinemia; B lymphocyte; plasma cell; CHRONIC LYMPHOCYTIC-LEUKEMIA; COPY NUMBER ABNORMALITIES; DOWN-REGULATION; B-LYMPHOCYTES; MULTIPLE-MYELOMA; HODGKIN-LYMPHOMA; DIFFERENTIATION; IDENTIFICATION; SURVIVAL; MIRNA;
D O I
10.1038/bcj.2011.25
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) are involved in the regulation of many cellular processes including hematopoiesis, with the aberrant expression of differentiation-stage specific miRNA associated with lymphomagenesis. miRNA profiling has been essential for understanding the underlying biology of many hematological malignancies; however the miRNA signature of the diverse tumor clone associated with Waldenstrom's macroglobulinemia (WM), consisting of B lymphocytes, plasmacytes and lymphoplasmacytic cells, has not been characterized. We have investigated the expression of over 13 000 known and candidate miRNAs in both CD19(+) and CD138(+) WM tumor cells, as well as in their malignant and non-malignant counterparts. Although neither CD19(+) nor CD138(+) WM cells were defined by a distinct miRNA profile, the combination of all WM cells revealed a unique miRNA transcriptome characterized by the dysregulation of many miRNAs previously identified as crucial for normal B-cell lineage differentiation. Specifically, miRNA-9*/152/182 were underexpressed in WM, whereas the expression of miRNA-21/125b/181a/193b/223/363 were notably increased (analysis of variance; P<0.0001). Future studies focusing on the effects of these dysregulated miRNAs will provide further insight into the mechanisms responsible for the pathogenesis of WM. Blood Cancer Journal (2011) 1, e24; doi: 10.1038/bcj.2011.25; published online 17 June 2011
引用
收藏
页码:e24 / e24
页数:9
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