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Inflammatory Bone Marrow Mesenchymal Stem Cells in Multiple Myeloma: Transcriptional Signature and In Vitro Modeling.
Wang, Lei; Yi, Weijun; Ma, Li; Lecea, Emily; Hazlehurst, Lori A; Adjeroh, Donald A; Hu, Gangqing.
Afiliação
  • Wang L; Department of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26505, USA.
  • Yi W; Department of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26505, USA.
  • Ma L; Lane Department of Computer Science & Electrical Engineering, West Virginia University, Morgantown, WV 26506, USA.
  • Lecea E; Department of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26505, USA.
  • Hazlehurst LA; Department of Microbiology, Immunology & Cell Biology, West Virginia University, Morgantown, WV 26505, USA.
  • Adjeroh DA; WVU Cancer Institute, West Virginia University, Morgantown, WV 26506, USA.
  • Hu G; Department of Pharmaceutical Sciences, School of Pharmacy, West Virginia University, Morganton, WV 26506, USA.
Cancers (Basel) ; 15(21)2023 Oct 26.
Article em En | MEDLINE | ID: mdl-37958322
ABSTRACT
Bone marrow mesenchymal stem cells (BM MSCs) play a tumor-supportive role in promoting drug resistance and disease relapse in multiple myeloma (MM). Recent studies have discovered a sub-population of MSCs, known as inflammatory MSCs (iMSCs), exclusive to the MM BM microenvironment and implicated in drug resistance. Through a sophisticated analysis of public expression data from unexpanded BM MSCs, we uncovered a positive association between iMSC signature expression and minimal residual disease. While in vitro expansion generally results in the loss of the iMSC signature, our meta-analysis of additional public expression data demonstrated that cytokine stimulation, including IL1-ß and TNF-α, as well as immune cells such as neutrophils, macrophages, and MM cells, can reactivate the signature expression of iMSCs to varying extents. These findings underscore the importance and potential utility of cytokine stimulation in mimicking the gene expression signature of early passage of iMSCs for functional characterizations of their tumor-supportive roles in MM.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2023 Tipo de documento: Article