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Leukemia ; 12(8): 1266-71, 1998 Aug.
Article in English | MEDLINE | ID: mdl-9697882

ABSTRACT

Mantle cell lymphomas (MCL) are morphologically and immunophenotypically distinctive lymphoid neoplasms characterised by overexpression of cyclin D1. Recent studies have suggested that co-operating aberrations of cell cycle associated genes may provide a growth advantage to a tumour. To address this issue further, we investigated five typical and three aggressive (blastoid) MCL for alterations in the cell cycle regulating genes p15, p16, CDK4, Rb and p53. In 3/3 aggressive cases with cyclin D1 overexpression we found aberration of at least one additional gene. One case showed diminished expression of the retinoblastoma protein (pRb); one case harboured deletion of both p15 and p16; and one case exhibited both deletion of p16 and point mutation of p53. However, we also identified two typical cases which in addition to cyclin D1 overexpression exhibited diminished pRb expression and p15 and p16 hypermethylation, respectively. Our findings confirm and extend other recent investigations and indicate that co-operating genetic alterations of cell cycle-associated genes may contribute to the pathogenesis of MCL.


Subject(s)
Cell Cycle Proteins , Genes, cdc , Lymphoma, Non-Hodgkin/genetics , Proto-Oncogene Proteins , Tumor Suppressor Proteins , Adult , Aged , Aged, 80 and over , Cyclin D1/metabolism , Cyclin-Dependent Kinase 4 , Cyclin-Dependent Kinase Inhibitor p15 , Cyclin-Dependent Kinase Inhibitor p16/metabolism , Cyclin-Dependent Kinases/metabolism , Female , Genotype , Humans , Male , Middle Aged , Phenotype , Retinoblastoma Protein/metabolism , Transcription Factors/metabolism , Tumor Suppressor Protein p53/metabolism
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