Literature DB >> 24657661

Exosome-mediated crosstalk between chronic myelogenous leukemia cells and human bone marrow stromal cells triggers an interleukin 8-dependent survival of leukemia cells.

Chiara Corrado1, Stefania Raimondo1, Laura Saieva1, Anna Maria Flugy1, Giacomo De Leo1, Riccardo Alessandro2.   

Abstract

Chronic myelogenous leukemia (CML) is a myeloproliferative disorder characterized by the Bcr-Abl oncoprotein with constitutive tyrosine kinase activity. Exosomes are nanovesicles released by cancer cells that are involved in cell-to-cell communication thus potentially affecting cancer progression. It is well known that bone marrow stromal microenvironment contributes to disease progression through the establishment of a bi-directional crosstalk with cancer cells. Our hypothesis is that exosomes could have a functional role in this crosstalk. Interleukin-8 (IL 8) is a proinflammatory chemokine that activates multiple signalling pathways downstream of two receptors (CXCR1 and CXCR2). We demonstrated that exosomes released from CML cells stimulate bone marrow stromal cells to produce IL 8 that, in turn, is able to modulate both in vitro and in vivo the leukemia cell malignant phenotype.
Copyright © 2014 Elsevier Ireland Ltd. All rights reserved.

Entities:  

Keywords:  Bone marrow stromal cells; Chronic myelogenous leukemia; Exosomes; Interleukin 8; Tumour microenvironment

Mesh:

Substances:

Year:  2014        PMID: 24657661     DOI: 10.1016/j.canlet.2014.03.009

Source DB:  PubMed          Journal:  Cancer Lett        ISSN: 0304-3835            Impact factor:   8.679


  73 in total

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8.  BCR-ABL1-positive microvesicles malignantly transform human bone marrow mesenchymal stem cells in vitro.

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Review 9.  Understanding the bone marrow microenvironment in hematologic malignancies: A focus on chemokine, integrin, and extracellular vesicle signaling.

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