Gene expression profiling reveals differences in microenvironment interaction between patients with chronic lymphocytic leukemia expressing high versus low ZAP70 mRNA

被引:28
作者
Stamatopoulos, Basile [1 ]
Haibe-Kains, Benjamin [2 ,3 ]
Equeter, Carole [2 ]
Meuleman, Nathalie
Soree, Anne
De Bruyn, Cecile
Hanosset, Delphine
Bron, Dominique
Martiat, Philippe
Lagneaux, Laurence
机构
[1] Univ Libre Bruxelles, Inst Jules Bordet, Lab Hematol Expt, Fac Med, B-1000 Brussels, Belgium
[2] Univ Libre Bruxelles, Inst Jules Bordet, Funct Genom & Translat Res Unit, Fac Med, B-1000 Brussels, Belgium
[3] Univ Libre Bruxelles, Fac Sci, Machine Learning Grp, B-1000 Brussels, Belgium
来源
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL | 2009年 / 94卷 / 06期
关键词
chronic lymphocytic leukemia; ZAP70; microarrays; microenvironment; prognosis; ZAP-70; EXPRESSION; LIPOPROTEIN-LIPASE; CD38; MUTATION STATUS; GENOMIC ABERRATIONS; DISEASE PROGRESSION; PROTEIN EXPRESSION; PROGNOSTIC-FACTOR; B-CELLS; SURVIVAL;
D O I
10.3324/haematol.2008.002626
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Zeta-associated protein 70 (ZAP70) is a widely recognized prognostic factor in chronic lymphocytic leukemia, but mechanisms by which its higher expression leads to a poor outcome must still be fully explained. Design and Methods In an attempt to unveil unfavorable cellular properties linked to high ZAP70 expression, we used gene expression profiling to identify genes associated with disparities in B cells from chronic lymphocytic leukemia patients expressing high versus low ZAP70 mRNA, measured by quantitative real-time PCR. Two groups of 7 patients were compared, selected on the basis of either high or low ZAP70 mRNA expression. Results Twenty-seven genes were differentially expressed with an FDR<10%, and several genes were significant predictors of treatment-free survival (TFS) and/or overall survival; PDE8A and FCRL family genes (down-regulated in ZAP70(+) patients) could predict TFS and overall survival; ITGA4 mRNA (up-regulated in ZAP70(+) patients) could significantly predict overall survival. Importantly, gene set enrichment analysis revealed overrepresentation of adhesion/migration genes. We therefore investigated in vitro adhesion/migration capacity of chronic lymphocytic leukemia cells into a stromal microenvironment or in response to conditioned medium. We showed that ZAP70(+) cells had better adhesion/migration capacities and only ZAP70(+) patient cells responded to microenvironment contact by CXCR4 downregulation. Conclusions We concluded that several prognostic factors are the reflection of micro environment interactions and that the increased adhesion/migratory capacity of ZAP70(+) cells in their microenvironment can explain their better survival and thus the aggressiveness of the disease.
引用
收藏
页码:790 / 799
页数:10
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