Tschan M P, Peters U R, Cajot J F, Betticher D C, Fey M F, Tobler A
Department of Clinical Research, University of Berne, Switzerland.
Br J Haematol. 1999 Sep;106(3):644-51. doi: 10.1046/j.1365-2141.1999.01617.x.
Cyclin-dependent kinase inhibitors (CKIs) are important for the differentiation of cells in various tissues. In acute myeloid leukaemia (AML) the cells accumulate at particular stages of myeloid maturation. We therefore analysed the expression pattern of different CKIs in fresh samples of AML patients and compared it with that in CD34+ progenitor and normal differentiated myeloid cells. Competitive RT-PCR and Western analysis revealed a significantly higher expression of p18INK4c and p19INK4d in leukaemic and CD34+ progenitor cells than in granulocytes and monocytes. A different pattern was seen for p27Kip1 and p57Kip2 expression being low in leukaemic cells but high in normal immature and differentiated cells. No marked differences were found in p15INK4b and p21Cip1 mRNA expression between leukaemic and CD34+ progenitor or mature myeloid cells. Our findings therefore indicate that high expression of p18INK4c and p19INK4d in haemopoietic progenitor and leukaemic blast cells may contribute to the premature differentiation block seen in AML.
细胞周期蛋白依赖性激酶抑制剂(CKIs)对各种组织中细胞的分化很重要。在急性髓系白血病(AML)中,细胞在髓系成熟的特定阶段积累。因此,我们分析了AML患者新鲜样本中不同CKIs的表达模式,并将其与CD34 +祖细胞和正常分化的髓系细胞中的表达模式进行比较。竞争性逆转录聚合酶链反应(RT-PCR)和蛋白质免疫印迹分析显示,与粒细胞和单核细胞相比,白血病细胞和CD34 +祖细胞中p18INK4c和p19INK4d的表达明显更高。p27Kip1和p57Kip2的表达模式不同,白血病细胞中表达低,而正常未成熟和分化细胞中表达高。白血病细胞与CD34 +祖细胞或成熟髓系细胞之间的p15INK4b和p21Cip1 mRNA表达没有明显差异。因此,我们的研究结果表明,造血祖细胞和白血病母细胞中p18INK4c和p19INK4d的高表达可能导致AML中出现的过早分化阻滞。