Chen Y, Cipriano S, Sarkar F, Ware J, Arenkiel J
VIRGINIA COMMONWEALTH UNIV,MED COLL VIRGINIA,DEPT PATHOL,RICHMOND,VA 23298.
Int J Oncol. 1995 Oct;7(4):889-93. doi: 10.3892/ijo.7.4.889.
The p21(WAF1) gene encodes a cyclin-dependent kinase inhibitor and plays an important role in controlling the cell cycle. Its expression can be induced through wild-type p53-dependent or -independent pathways. Since the p53-dependent pathway is disrupted in more than 50% of human tumors, we wondered whether the p53-independent pathway is also altered during tumor progression. In the present study, we have determined p21(WAF1) induction by mitogenic stimuli, which is known to be a p53-independent process. p21(WAF1) is induced by mitogenic stimuli in all cell lines tested regardless of the status of p53, i.e. wild-type, wild-type inactivated by SV40T or mutant, and the transformation of cells from immortal to tumorigenic and to metastatic. These results indicate that the p53-independent induction of p21(WAF1) pathway is preserved during tumor progression.
p21(WAF1)基因编码一种细胞周期蛋白依赖性激酶抑制剂,在控制细胞周期中起重要作用。其表达可通过野生型p53依赖性或非依赖性途径诱导。由于超过50%的人类肿瘤中p53依赖性途径被破坏,我们想知道在肿瘤进展过程中p53非依赖性途径是否也发生改变。在本研究中,我们确定了有丝分裂原刺激诱导p21(WAF1)的情况,已知这是一个p53非依赖性过程。无论p53状态如何,即野生型、被SV40T灭活的野生型或突变型,以及细胞从永生化转变为致瘤性和转移性,有丝分裂原刺激均可在所有测试的细胞系中诱导p21(WAF1)。这些结果表明,在肿瘤进展过程中,p21(WAF1)途径的p53非依赖性诱导得以保留。