Robust isolation of malignant plasma cells in multiple myeloma.
Author
Summary, in English
Molecular characterization of malignant plasma cells is increasingly important for diagnostic and therapeutic stratification in multiple myeloma (MM). However, the malignant plasma cells represent a relatively small subset of bone marrow cells, and need to be enriched prior to analysis. Currently, the cell surface marker CD138 (SDC1) is used for this enrichment, but has an important limitation in that its expression decreases rapidly after sampling. Seeking alternatives to CD138, we performed a computational screen for myeloma plasma cell markers and evaluated seven candidates systematically. Our results conclusively show that the markers CD319 (SLAMF7/CS1) and CD269 (TNFRSF17/BCMA) are considerably more robust than CD138, and enable isolation of myeloma plasma cells under more diverse conditions, including in samples that have been delayed or frozen. Our results form the basis of improved procedures for characterizing cases of multiple myeloma in clinical practice.
Department/s
- Hematogenomics
- Myeloma research group
- Division of Hematology and Transfusion Medicine
- Division of Clinical Genetics
- Department of Clinical Sciences, Malmö
- BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation
Publishing year
2014
Language
English
Pages
1336-1340
Publication/Series
Blood
Volume
123
Issue
9
Links
Document type
Journal article
Publisher
American Society of Hematology
Topic
- Hematology
Status
Published
Project
- Genetic predisposition for multiple myeloma
Research group
- Hematogenomics
- Myeloma research group
ISBN/ISSN/Other
- ISSN: 1528-0020