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EWSR1 overexpression is a pro-oncogenic event in multiple myeloma.

Authors :
Nishiyama D
Chinen Y
Isa R
Fujibayashi Y
Kuwahara-Ota S
Yamaguchi J
Takimoto-Shimomura T
Matsumura-Kimoto Y
Tsukamoto T
Shimura Y
Kobayashi T
Horiike S
Taniwaki M
Handa H
Kuroda J
Source :
International journal of hematology [Int J Hematol] 2021 Mar; Vol. 113 (3), pp. 381-394. Date of Electronic Publication: 2020 Oct 23.
Publication Year :
2021

Abstract

Multiple myeloma (MM) is cytogenetically, genetically and molecularly heterogenous even among subclones in one patient, therefore, it is essential to identify both frequent and patient-specific drivers of molecular abnormality. Following previous molecular investigations, we in this study investigated the expression patterns and function of the Ewing sarcoma breakpoint region 1 (EWSR1) gene in MM. The EWSR1 transcriptional level in CD138-positive myeloma cells was higher in 36.4% of monoclonal gammopathy of undetermined significance, in 67.4% of MM patients compared with normal plasma cells, and significantly higher in ten human myeloma-derived cell lines (HMCLs) examined. EWSR1 gene knockdown caused growth inhibition with an increase of apoptotic cells in NCI-H929 and KMS-12-BM cells. Gene expression profiling using microarray analysis suggested EWSR1 gene knockdown caused transcriptional modulation of several genes associated with processes such as cell proliferation, cell motility, cell metabolism, and gene expression. Of particular, EWSR1 gene knockdown caused upregulation of let-7c and downregulation of its known targets K-RAS and AKT. Finally, our analysis using community database suggested that high EWSR1 expression positively associates with poor prognosis and advanced disease stage in MM. These findings suggest that EWSR1 overexpression is a pro-oncogenic molecular abnormality that may participate in MM progression.

Details

Language :
English
ISSN :
1865-3774
Volume :
113
Issue :
3
Database :
MEDLINE
Journal :
International journal of hematology
Publication Type :
Academic Journal
Accession number :
33095415
Full Text :
https://doi.org/10.1007/s12185-020-03027-0