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

C Corrado, S Raimondo, L Saieva, AM Flugy, G De Leo… - Cancer letters, 2014 - Elsevier
C Corrado, S Raimondo, L Saieva, AM Flugy, G De Leo, R Alessandro
Cancer letters, 2014Elsevier
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 …
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.
Elsevier