TY - JOUR
T1 - Profiling of circulating exosomal miRNAs in patients with Waldenström Macroglobulinemia
AU - Bouyssou, Juliette M.
AU - Liu, Chia Jen
AU - Bustoros, Mark
AU - Sklavenitis-Pistofidis, Romanos
AU - Aljawai, Yosra
AU - Manier, Salomon
AU - Yosef, Amir
AU - Sacco, Antonio
AU - Kokubun, Katsutoshi
AU - Tsukamoto, Shokichi
AU - Glen, Adriana Perilla
AU - Huynh, Daisy
AU - Castillo, Jorge J.
AU - Treon, Steven P.
AU - Leblond, Veronique
AU - Hermine, Olivier
AU - Roccaro, Aldo M.
AU - Ghobrial, Irene M.
AU - Capelletti, Marzia
N1 - Publisher Copyright:
© 2018 Hsieh et al.
PY - 2018/10
Y1 - 2018/10
N2 - Waldenstrom Macroglobulinemia (WM) is a low-grade B-cell lymphoma characterized by disease progression from IgM MGUS to asymptomatic and then symptomatic disease states. We profiled exosomes from the peripheral blood of patients with WMat different stages (30 smoldering/asymptomatic WM, 44 symptomatic WM samples and 10 healthy controls) to define their role as potential biomarkers of disease progression. In this study, we showed that circulating exosomes and their miRNA content represent unique markers of the tumor and its microenvironment. We observed similar levels of miRNAs in exosomes from patients with asymptomatic (smoldering) and symptomatic WM, suggesting that environmental and clonal changes occur in patients at early stages of disease progression before symptoms occur. Moreover, we identified a small group of miRNAs whose expression correlated directly or inversely with the disease status of patients, notably the known tumor suppressor miRNAs let-7d and the oncogene miR-21 as well as miR-192 and miR-320b. The study of these miRNAs' specific effect inWMcells could help us gain further insights on the mechanisms underlying WM pathogenesis and reveal their potential as novel therapeutic targets for this disease.
AB - Waldenstrom Macroglobulinemia (WM) is a low-grade B-cell lymphoma characterized by disease progression from IgM MGUS to asymptomatic and then symptomatic disease states. We profiled exosomes from the peripheral blood of patients with WMat different stages (30 smoldering/asymptomatic WM, 44 symptomatic WM samples and 10 healthy controls) to define their role as potential biomarkers of disease progression. In this study, we showed that circulating exosomes and their miRNA content represent unique markers of the tumor and its microenvironment. We observed similar levels of miRNAs in exosomes from patients with asymptomatic (smoldering) and symptomatic WM, suggesting that environmental and clonal changes occur in patients at early stages of disease progression before symptoms occur. Moreover, we identified a small group of miRNAs whose expression correlated directly or inversely with the disease status of patients, notably the known tumor suppressor miRNAs let-7d and the oncogene miR-21 as well as miR-192 and miR-320b. The study of these miRNAs' specific effect inWMcells could help us gain further insights on the mechanisms underlying WM pathogenesis and reveal their potential as novel therapeutic targets for this disease.
UR - http://www.scopus.com/inward/record.url?scp=85054464194&partnerID=8YFLogxK
U2 - 10.1371/journal.pone.0204589
DO - 10.1371/journal.pone.0204589
M3 - Article
C2 - 30286096
AN - SCOPUS:85054464194
SN - 1932-6203
VL - 13
JO - PLoS ONE
JF - PLoS ONE
IS - 10
M1 - e0204589
ER -