TY - JOUR
T1 - The expression of CXCR4 is down-regulated on the CD34+ cells of patients with myelofibrosis with myeloid metaplasia
AU - Rosti, Vittorio
AU - Massa, Margherita
AU - Vannucchi, Alessandro M.
AU - Bergamaschi, Gaetano
AU - Campanelli, Rita
AU - Pecci, Alessandro
AU - Viarengo, Gianluca
AU - Meli, Valentina
AU - Marchetti, Monia
AU - Guglielmelli, Paola
AU - Bruno, Edward
AU - Xu, Mingjiang
AU - Hoffman, Ronald
AU - Barosi, Giovanni
N1 - Funding Information:
Research Grant Support: This work was supported by a grant (CS30, 2003) from Istituto Superiore di Sanità; a grant from the Italian Ministry of Health (Ricerca Finalizzata 2002), a grant from MIUR (2003, #06488803); a grant from Associazione Italiana per la Ricerca sul Cancro (Milano) and the MPD Research Consortium funded by the National Cancer Institute (CA P01 CA 108671-01A2).
PY - 2007
Y1 - 2007
N2 - Purpose: We studied the expression of the chemokine receptor CXCR4 on circulating CD34+ cells of patients with myelofibrosis with myeloid metaplasia (MMM), and examined its relationship to the severity of disease. Patients and methods: Surface and intracellular CXCR4 expression were measured flow cytometrically in 84 consecutive MMM patients, 16 patients with polycythemia vera (PV), and 20 healthy subjects. In 23 MMM patients, CXCR4 gene expression level was also quantitated by real time-RT-PCR in CD34+ cells. Results: The expression of CXCR4 on circulating CD34+ cells was significantly reduced in patients with MMM (P < 0.001) as compared to normal controls and patients with PV (P = 0.01). The levels of CXCR4 mRNA in CD34+ cells were lower in patients with MMM as compared with normal subjects, and were directly correlated with the degree of CXCR4 surface expression, demonstrating that transcriptional defects were the major cause for receptor down-regulation. No statistical association was found between JAK2V617F mutational status and the extent of CXCR4 down-regulation. CXCR4 expression on CD34+ cells inversely correlated with the number of circulating CD34+ cells (R = - 0.55; P < 0.001), and was severely down-regulated in high risk patients and patients with a high "myelodepletion severity index". CXCR4 down-regulation was associated with advanced patient age, the presence of severe anemia, thrombocytopenia, and degree of bone marrow fibrosis. Conclusions: Reduced expression of CXCR4 by CD34+ cells is a characteristic of MMM which is associated with the constitutive mobilization of CD34+ cells and occurs in patients with advanced forms of the disease.
AB - Purpose: We studied the expression of the chemokine receptor CXCR4 on circulating CD34+ cells of patients with myelofibrosis with myeloid metaplasia (MMM), and examined its relationship to the severity of disease. Patients and methods: Surface and intracellular CXCR4 expression were measured flow cytometrically in 84 consecutive MMM patients, 16 patients with polycythemia vera (PV), and 20 healthy subjects. In 23 MMM patients, CXCR4 gene expression level was also quantitated by real time-RT-PCR in CD34+ cells. Results: The expression of CXCR4 on circulating CD34+ cells was significantly reduced in patients with MMM (P < 0.001) as compared to normal controls and patients with PV (P = 0.01). The levels of CXCR4 mRNA in CD34+ cells were lower in patients with MMM as compared with normal subjects, and were directly correlated with the degree of CXCR4 surface expression, demonstrating that transcriptional defects were the major cause for receptor down-regulation. No statistical association was found between JAK2V617F mutational status and the extent of CXCR4 down-regulation. CXCR4 expression on CD34+ cells inversely correlated with the number of circulating CD34+ cells (R = - 0.55; P < 0.001), and was severely down-regulated in high risk patients and patients with a high "myelodepletion severity index". CXCR4 down-regulation was associated with advanced patient age, the presence of severe anemia, thrombocytopenia, and degree of bone marrow fibrosis. Conclusions: Reduced expression of CXCR4 by CD34+ cells is a characteristic of MMM which is associated with the constitutive mobilization of CD34+ cells and occurs in patients with advanced forms of the disease.
KW - CXCR4
KW - Mobilization
KW - Myelofibrosis
KW - SDF-1
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U2 - 10.1016/j.bcmd.2007.01.003
DO - 10.1016/j.bcmd.2007.01.003
M3 - Article
C2 - 17350297
AN - SCOPUS:34047097012
SN - 1079-9796
VL - 38
SP - 280
EP - 286
JO - Blood Cells, Molecules, and Diseases
JF - Blood Cells, Molecules, and Diseases
IS - 3
ER -