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  • Sadeghi, LKarolinska Institutet (author)

Differential B-Cell Receptor Signaling Requirement for Adhesion of Mantle Cell Lymphoma Cells to Stromal Cells

  • Article/chapterEnglish2020

Publisher, publication year, extent ...

  • 2020-05-02
  • MDPI AG,2020

Numbers

  • LIBRIS-ID:oai:prod.swepub.kib.ki.se:143894730
  • http://kipublications.ki.se/Default.aspx?queryparsed=id:143894730URI
  • https://doi.org/10.3390/cancers12051143DOI

Supplementary language notes

  • Language:English
  • Summary in:English

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  • Subject category:ref swepub-contenttype
  • Subject category:art swepub-publicationtype

Notes

  • Interactions between lymphoma cells and stromal cells play a key role in promoting tumor survival and development of drug resistance. We identified differences in key signaling pathways between the JeKo-1 and REC-1 mantle cell lymphoma (MCL) cell lines, displaying different patterns of stromal cell adhesion and chemotaxis towards stroma-conditioned medium. The identified adhesion-regulated genes reciprocated important aspects of microenvironment-mediated gene modulation in MCL patients. Five-hundred and ninety genes were differently regulated between the cell lines upon adhesion to stromal cells, while 32 genes were similarly regulated in both cell lines. Regulation of B-cell Receptor (BCR) signature genes in adherent cells was specific for JeKo-1. Inhibition of BCR using siRNA or clinically approved inhibitors, Ibrutinib and Acalabrutinib, decreased adhesion of JeKo-1, but not REC-1 cells. Cell surface levels of chemokine receptor CXCR4 were higher in JeKo-1, facilitating migration and adhesion of JeKo-1 but not REC-1 cells. Surface levels of ICAM1 adhesion protein differ for REC-1 and JeKo-1. While ICAM1 played a positive role in adherence of both cell lines to stromal cells, S1PR1 had an inhibitory effect. Our results provide a model framework for further investigation of mechanistic differences in patient-response to new pathway-specific drugs.

Added entries (persons, corporate bodies, meetings, titles ...)

  • Arvidsson, G (author)
  • Merrien, MKarolinska Institutet (author)
  • Wasik, AMKarolinska Institutet (author)
  • Gorgens, AKarolinska Institutet (author)
  • Smith, CIEKarolinska Institutet (author)
  • Sander, BKarolinska Institutet (author)
  • Wright, APKarolinska Institutet (author)
  • Karolinska Institutet (creator_code:org_t)

Related titles

  • In:Cancers: MDPI AG12:52072-6694

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