Programmed cell death protein 4 suppresses CDK1/cdc2 via induction of p21Waf1/Cip1

被引:123
作者
Göke, R
Barth, P
Schmidt, A
Samans, B
Lankat-Buttgereit, B
机构
[1] Univ Marburg, Clin Res Unit Gastrointestinal Endocrinol, D-35033 Marburg, Germany
[2] Univ Marburg, Inst Pathol, D-35033 Marburg, Germany
[3] Univ Marburg, Inst Med Biometry & Epidemiol, D-35033 Marburg, Germany
来源
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY | 2004年 / 287卷 / 06期
关键词
tumor growth; cell cycle; tumor suppressor gene;
D O I
10.1152/ajpcell.00025.2004
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
We show that the recently discovered tumor suppressor pdcd4 represses the transcription of the mitosis-promoting factor cyclin-dependent kinase (CDK) 1/cdc2 via upregulation of p21(Waf1)/ Cip1. p21(Waf1/Cip1) inhibits CDK4/6 and CDK2. Decrease of CDK4/6 and CDK2 enhances the binding of pRb to E2F/DP, which in turn together bind to and repress the cdc2 promoter. Upregulation of CDK1/cdc2 accompanied by a malignant change was previously reported in colon cancer. We show that expression of pdcd4 as an indirect suppressor of CDK1/cdc2 is lost in progressed carcinomas of lung, breast, colon, and prostate. Furthermore, it seems that localization and expression of pdcd4 directly correlate with tumor progression. Finally, the CDK1/cdc2 inhibitor roscovitine reduces the proliferation of several tumor cell lines, suggesting that inhibition of CDK1/cdc2 may be a useful strategy against malignant transformation. Therefore, pdcd4 might serve as a novel target for antineoplastic therapies.
引用
收藏
页码:C1541 / C1546
页数:6
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