Constitutive expression of the AP-1 transcription factors c-jun, junD, junB, and c-fos and the marginal zone B-cell transcription factor notch2 in splenic marginal zone lymphoma

被引:37
作者
Troen, G [1 ]
Nygaard, V
Jenssen, TK
Ikonomou, IM
Tierens, A
Matutes, E
Gruszka-Westwood, A
Catovsky, D
Myklebost, O
Lauritzsen, G
Hovig, E
Delabie, J
机构
[1] Univ Oslo, Norwegian Radium Hosp, Dept Pathol, N-0310 Oslo, Norway
[2] Norwegian Radium Hosp, Dept Tumor Biol, N-0310 Oslo, Norway
[3] Norwegian Radium Hosp, Dept Oncol, N-0310 Oslo, Norway
[4] Pubgene Inc, Oslo, Norway
[5] Inst Canc Res, Dept Acad Haematol & Cytogenet, London SW3 6JB, England
[6] Royal Marsden Hosp, London SW3 6JJ, England
关键词
D O I
10.1016/S1525-1578(10)60525-9
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Splenic marginal zone lymphoma (SMZL) is a lymphoma type of putative marginal zone B-cell origin. No specific genetic alterations have yet been demonstrated in SMZL. Clinically, SMZL is a low-grade B-cell non-Hodgkin lymphoma. However, the presence of p53 mutation, 7q22-7q32 deletion or the absence of somatic hypermutations of immunoglobulin genes has been correlated with a worse prognosis. In this study, we analyzed genome-wide gene expression of 24 cases of SMZL using the microarray technique. The AP-1 transcription factors c-jun, junD, junB, and c-fos as well as Notch2 were found to be specifically upregulated. These data were confirmed by real-time PCR and immunohistochemical staining of tissue sections. The absence of concordant high expression of the MAP kinases, the signaling cascade leading to AP-1 up-regulation, suggests autoregulation of the AP-1 transcription factors and an important role in SMZL oncogenesis. High expression of Notch2, a transcription factor that induces marginal zone B-cell differentiation, is highly suggestive for a marginal zone B-cell origin of SMZL. In addition, SMZL with the 7q deletion showed high expression of TGF-beta1 and low expression of the DNA helicase XPB, a crucial part of the nucleotide excision repair complex, possibly explaining the more aggressive clinical course of those cases.
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页码:297 / 307
页数:11
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