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CXCR4 expression of multiple myeloma as a dynamic process: influence of therapeutic agents.

Authors :
Bögelein, Anna
Stolzenburg, Antje
Eiring, Patrick
Lückerath, Katharina
Munawar, Umair
Werner, Rudolf
Schirbel, Andreas
Samnick, Samuel
Kortüm, Klaus Martin
Sauer, Markus
Lapa, Constantin
Buck, Andreas K.
Source :
Leukemia & Lymphoma; Oct2022, Vol. 63 Issue 10, p2393-2402, 10p
Publication Year :
2022

Abstract

Chemokine receptors represent novel targets for treatment of multiple myeloma (MM). However, CXCR4 expression appears to be highly dynamic. This in vitro study investigated the impact of commonly used anti-myeloma agents on CXCR4 expression. Established human myeloma cell lines as well as patient-derived CD138<superscript>+</superscript> plasma cells were exposed to antineoplastic drugs. Cells were analyzed for CXCR4 expression by flow cytometry and direct stochastic optical reconstruction microscopy (dSTORM). In addition, cellular uptake of <superscript>68</superscript>Ga-Pentixafor, a PET radiotracer for noninvasive assessment of CXCR4 expression in vivo, was assessed. CXCR4 expression was highly variable and turned out to be substance, dose and time dependent. Treatment with bortezomib was associated with reduced expression, while dexamethasone and doxorubicin significantly increased expression of CXCR4. Combination of these compounds further increased CXCR4 expression. In conclusion, drugs or combination of drugs can induce CXCR4 expression in myeloma cells. Hence, pretreatment may impact on response to CXCR4-based therapies. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10428194
Volume :
63
Issue :
10
Database :
Complementary Index
Journal :
Leukemia & Lymphoma
Publication Type :
Academic Journal
Accession number :
159584046
Full Text :
https://doi.org/10.1080/10428194.2022.2074986