Kokunai T, Izawa I, Tamaki N
Department of Neurosurgery, Kobe University School of Medicine, Japan.
Int J Cancer. 1998 Feb 9;75(4):643-8. doi: 10.1002/(sici)1097-0215(19980209)75:4<643::aid-ijc24>3.0.co;2-8.
p21WAF1/CIP1 is a downstream mediator of p53 and mediates growth arrest by inhibiting the action of G1 cyclin-dependent kinases. Since cellular differentiation is frequently characterized by G1 arrest, we examined whether p21WAF1/CIP1 overexpression would induce growth suppression and differentiation in p53-defective human glioma cells. Overexpression of p21WAF1/CIP1 resulted in an accumulation of cells in G1, altered morphology, growth arrest and cell differentiation. The extent of cell differentiation correlated with the level of p21WAF1/CIP1 as well as of proliferating cell nuclear antigen, cyclin E, and cdk 2, which associates with p21WAF1/CIP1. Our data suggest that gene transfer of p21WAF1/CIP1 may arrest glioma cell growth in vivo by committing malignant glioma cells to a pathway of terminal differentiation.
p21WAF1/CIP1是p53的下游介质,通过抑制G1细胞周期蛋白依赖性激酶的作用来介导生长停滞。由于细胞分化通常以G1期停滞为特征,我们研究了p21WAF1/CIP1的过表达是否会在p53缺陷的人胶质瘤细胞中诱导生长抑制和分化。p21WAF1/CIP1的过表达导致细胞在G1期积累、形态改变、生长停滞和细胞分化。细胞分化程度与p21WAF1/CIP1以及增殖细胞核抗原、细胞周期蛋白E和与p21WAF1/CIP1相关的细胞周期蛋白依赖性激酶2的水平相关。我们的数据表明,p21WAF1/CIP1的基因转移可能通过使恶性胶质瘤细胞进入终末分化途径来在体内阻止胶质瘤细胞生长。