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

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 hematologica...

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Published inBlood cancer journal (New York) Vol. 1; no. 6; p. e24
Main Authors Hodge, L S, Elsawa, S F, Grote, D M, Price-Troska, T L, Asmann, Y W, Fonseca, R, Gertz, M A, Witzig, T E, Novak, A J, Ansell, S M
Format Journal Article
LanguageEnglish
Published London Nature Publishing Group UK 01.06.2011
Springer Nature B.V
Nature Publishing Group
Subjects
631/250/2502/2055
692/699/67/1990
Biomedical and Life Sciences
Biomedicine
Cancer Research
Hematology
Oncology
Original
original-article
B lymphocyte
microRNA
Waldenstrom's macroglobulinemia
plasma cell
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Abstract 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.
AbstractList 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.
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.
Author Hodge, L S
Elsawa, S F
Fonseca, R
Gertz, M A
Ansell, S M
Asmann, Y W
Price-Troska, T L
Witzig, T E
Grote, D M
Novak, A J
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  surname: Ansell
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  email: ansell.stephen@mayo.edu
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/22829168$$D View this record in MEDLINE/PubMed
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Issue 6
Keywords B lymphocyte
microRNA
Waldenstrom's macroglobulinemia
plasma cell
Language English
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Snippet MicroRNAs (miRNAs) are involved in the regulation of many cellular processes including hematopoiesis, with the aberrant expression of differentiation-stage...
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692/699/67/1990
Biomedical and Life Sciences
Biomedicine
Cancer Research
Hematology
Oncology
Original
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Title MicroRNA expression in tumor cells from Waldenstrom's macroglobulinemia reflects both their normal and malignant cell counterparts
URI http://dx.doi.org/10.1038/bcj.2011.25
https://link.springer.com/article/10.1038/bcj.2011.25
https://www.ncbi.nlm.nih.gov/pubmed/22829168
https://www.proquest.com/docview/1785294854
https://search.proquest.com/docview/1028017278
https://pubmed.ncbi.nlm.nih.gov/PMC3255267
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