cdc25A and the splicing variant cdc25B2, but not cdc25B1, -B3 or -C, are over-expressed in aggressive human non-Hodgkin's lymphomas

cdc25 is a Family of phosphatases that activate the cyclin-dependent kinase s at different points of the cell cycle. cdc25A and -B, but not -C, have be en shown to have oncogenic potential, Three different splicing variants of the cdc25B gene, cdc25B1, -B2 and -B3, have also been identified. Experimen tal studies suggest that cdc25B2 may be more active in vivo than cdc25B3 an d -B1, but the relative expression of these splicing variants in human tumo rs is not. known. In this study, we have analyzed the expression of cdc25A, -B1, -B2, -B3 and -C mRNA in 9 non-neoplastic lymphoid samples, 89 non-Hod gkin's lymphomas and 9 hematological cancer cell lines by semi-quantitative RT-PCR, cdc25A, -B and -C protein expression was examined by Western blot. Normal peripheral blood lymphocytes and reactive tissues expressed cdc25B1 and -B3 mRNA and very low or undetectable levels of cdc25A, -B2 and -C, Hi gh levels of cdc25A and cdc25B2 were found in 35% and 39% of the tumors, re spectively, and they were more frequently observed in aggressive than in in dolent lymphomas, cdc25B1 and -B3 splice variants were detected in virtuall y all tumors, and no significant differences were found between high- and l ow-grade lymphomas, cdc25A and -B protein expression was also higher in agg ressive than in indolent lymphomas, cdc25C expression was relatively low in virtually all cases. In conclusion, these findings suggest that cdc25A and -B2, but not cdc25B1, -B3 and -C, are over-expressed in a relatively large number of malignant lymphomas and may participate in the pathogenesis of a ggressive variants. (C) 2000 Wiley-Liss, Inc.