Induction of miR-146a by multiple myeloma cells in mesenchymal stromal cells stimulates their pro-tumoral activity. Issue 1 (10th July 2016)

• Record Type: Journal Article
• Authors: De Veirman, Kim; Wang, Jinheng; Xu, Song; Leleu, Xavier; Himpe, Eddy; Maes, Ken; De Bruyne, Elke; Van Valckenborgh, Els; Vanderkerken, Karin; Menu, Eline; Van Riet, Ivan
• Is Part Of: Cancer letters. Volume 377:Issue 1(2016)
• Page Start: 17
• Page End: 24
• Publication Date: 2016-07-10
• Subjects: Multiple myeloma -- Mesenchymal stromal cell -- Exosomes -- miR-146a -- Notch pathway; Cancer -- Periodicals; Neoplasms -- Periodicals; Cancer -- Périodiques; Electronic journals; 616.994
• DOI: 10.1016/j.canlet.2016.04.024
• Languages: English
• ISSNs: 0304-3835

Abstract

Highlights: Multiple myeloma (MM) cells regulate 19 miRNAs in mesenchymal stromal cells (MSC). MM cell-derived exosomes transfer miR-146a into MSC. miR-146a promotes cytokine secretion in MSC, favoring MM cell growth and migration. Inhibition of the Notch pathway reduces miR-146a-induced cytokine secretion in MSC. Abstract: Mutual communication between multiple myeloma (MM) cells and mesenchymal stromal cells (MSC) plays a pivotal role in supporting MM progression. In MM, MSC exhibit a different genomic profile and dysregulated cytokine secretion compared to normal MSC, however the mechanisms involved in these changes are not fully understood. Here, we examined the miRNA changes in human MSC after culture with conditioned medium of MM cells and found 19 dysregulated miRNAs, including upregulated miR-146a. Moreover, exosomes derived from MM cells contained miR-146a and could be transferred into MSC. After overexpressing miR-146a in MSC, secretion of several cytokines and chemokines including CXCL1, IL6, IL-8, IP-10, MCP-1, and CCL-5 was elevated, resulting in the enhancement of MM cell viability and migration. DAPT, an inhibitor of the endogenous Notch pathway, was able to abrogate the miR-146a-induced increase of cytokines in MSC, suggesting the involvement of the Notch pathway. Taken together, our results demonstrate a positive feedback loop between MM cells and MSC: MM cells promote the increase of miR146a in MSC which leads to more cytokine secretion, which in turn favors MM cell growth and migration.