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Distinct gene expression patterns in chronic lymphocytic leukemia defined by usage of specific VH genes
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作者:

Kienle, D
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机构: Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany

Benner, A
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机构: Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany

Kröber, A
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机构: Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany

Winkler, D
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机构: Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany

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Bühler, A
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机构: Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany

Seiler, T
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机构: Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany

Jäger, UJ
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h-index: 0
机构: Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany

Lichter, P
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h-index: 0
机构: Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany

Döhner, H
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h-index: 0
机构: Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany

Stilgenbauer, S
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机构: Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany
机构:
[1] Univ Ulm, Dept Internal Med 3, D-89081 Ulm, Germany
[2] DKFZ, German Canc Res Ctr, Cent Unit Biostat, Heidelberg, Germany
[3] DKFZ, Div Mol Genet, Heidelberg, Germany
[4] Med Univ Vienna, Dept Internal Med 1, Vienna, Austria
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D O I:
10.1182/blood-2005-04-1483
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
The mutation status and usage of specific VH genes such as V3-21 and V1-69 are potentially independent pathogenic and prognostic factors in chronic lymphocytic leukemia (CLL). To investigate the role of antigenic stimulation, we analyzed the expression of genes involved in B-cell receptor (BCR) signaling/activation, cell cycle, and apoptosis control in CLL using these specific VH genes compared to VH mutated (VH-MUT) and VH unmutated (VH-UM) CLL not using these VH genes. V3-21 cases showed characteristic expression differences compared to VH-MUT (up: ZAP70 [or ZAP-70]; down: CCND2, P27) and VH-UM (down: PI3K, CCND2, P27, CDK4, BAX) involving several BCR-related genes. Similarly, there was a marked difference between VH unmutated cases using the V1-69 gene and VH-UM (up: FOS; down: BLNK, SYK, CDK4, TP53). Therefore, usage of specific VH genes appears to have a strong influence on the gene expression pattern pointing to antigen recognition and ongoing BCR stimulation as a pathogenic factor in these CLL subgroups.
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页码:2090 / 2093
页数:4
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