The Journal of molecular diagnostics : JMD · 2004
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.
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Trøen Gunhild, Nygaard Vigdis, Jenssen Tor-Kristian, Ikonomou Ida Münster, Tierens Anne, Matutes Estella, Gruszka-Westwood Alicja, Catovsky Daniel, Myklebost Ola, Lauritzsen Grete, Hovig Eivind, Delabie Jan
Аннотация
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 up-regulated. 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.
Предметные рубрики MeSH
AllelesChromosomes, Human, Pair 7DNADown-RegulationFluorescent DyesGene DeletionGene Expression Regulation, NeoplasticGenes, junGenes, p53HumansImmunohistochemistryLymphoma, B-CellMicrosatellite RepeatsMutationNucleic Acid HybridizationOligonucleotide Array Sequence AnalysisPolymerase Chain ReactionPrognosisProto-Oncogene Proteins c-fosProto-Oncogene Proteins c-junReceptor, Notch2Receptors, Cell SurfaceReverse Transcriptase Polymerase Chain ReactionTranscription Factor AP-1Transcription, GeneticUp-Regulation