Chromosomal aberrations in bone marrow mesenchymal stroma cells from patients with myelodysplastic syndrome and acute myeloblastic leukemia

被引:133
作者
Blau, Olga
Hofmann, Wolf-Karsten
Baldus, Claudia Dorothea
Thiel, Gundula
Serbent, Verena
Schuemann, Elke
Thiel, Eckhard
Blau, Igor Wolfgang
机构
[1] Univ Sch Med, Charite, Dept Hematol Oncol & Transfus Med, D-12200 Berlin, Germany
[2] Genet Lab, Berlin, Germany
[3] Out Patients Clin, Berlin, Germany
关键词
D O I
10.1016/j.exphem.2006.10.012
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. Bone marrow mesenchymal stroma cells (BMSC) are key components of the hematopoietic microenvironment. The question of whether BMSC from patients with hematological disorders have cytogenetic abnormalities is discussed controversially, some studies indicating that they are cytogenetically normal and others providing evidence of their aberrations. Patients and Methods. We performed standard and molecular cytogenetic analyses of both hematopoietic cells and BMSC from 31 patients with myelodysplastic syndrome (MDS, n = 18) and acute myeloid leukemia (AML, n = 13) and 7 healthy individuals. Mononuclear cells were isolated from fresh bone marrow aspirates at the time of initial diagnosis for cytogenetic analysis of hematopoietic cells (HC) and selection of BMSC. Results. Clonal cytogenetic aberrations were observed in HC from 8 (44%) MDS and 8 (61%) AML patients. Cytogenetic analyses of BMSC were successfully performed in 27 of the 31 cases. Structural chromosomal aberrations, including t(1;7), t(4;7), t(7;9), t(7;10), t(7;19), t(15;17), and others, were detectable in BMSC from 7 of 16 (44%) MDS and 6 of 11 (54%) AML patients. The breakpoints of chromosomes in BMSC were typical for leukemia aberrations. Two patients showed clonal chromosomal markers. Conclusions. BMSC from MDS and AML patients show chromosomal abnormalities. Although the majority of cytogenetic aberrations in BMSC were not clonal and differed from chromosomal markers in HC from the same individual, detection of typical chromosomal changes in BMSC suggests enhanced genetic susceptibility of these cells in MDS/AML. This may indicate potential involvement of BMSC in the pathophysiology of MDS/AML. (c) 2007 International Society for Experimental Hematology. Published by Elsevier Inc.
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页码:221 / 229
页数:9
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