p21waf1 control of epithelial cell cycle and cell fate

被引:130
作者
Weinberg, WC
Denning, MF
机构
[1] US FDA, CBER, DMA, Immunobiol Lab, Bethesda, MD 20892 USA
[2] Loyola Univ, Med Ctr, Dept Pathol, Maywood, IL 60153 USA
[3] Loyola Univ, Med Ctr, Cardinal Bernardin Canc Ctr, Maywood, IL 60153 USA
关键词
p21(WAF1); cell cycle; keratinocytes; cyclin-dependent kinase; cell transformation;
D O I
10.1177/154411130201300603
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
As a broad-acting cyclin-dependent kinase inhibitor, p21(WAF1) occupies a central position in the cell cycle regulation of self-renewing tissues such as oral mucosa and skin. In addition to regulating normal cell cycle progression decisions, p21(WAF1) integrates genotoxic insults into growth arrest and apoptotic signaling pathways that ultimately determine cell fate. As a result of its complex interactions with cell cycle machinery and response to mutagenic agents, p21(WAF1) also has stage-specific roles in epithelial carcinogenesis. Finally, a view is emerging of p21(WAF1) as not merely a cyclin-dependent kinase inhibitor, but also as a direct participant in regulating genes involved in growth arrest, senescence, and aging, thus providing an additional layer of control over matters of the cell cycle. This review discusses these various roles played by p21(WAF1) in cell cycle control, and attempts to relate these to epithelial cell biology, with special emphasis on keratinocytes. (Abbreviations used include the following: Brdu, 5-Bromo-2'-deoxyuridine; cdk, cyclin-dependent kinase; EGF, epidermal growth factor; KIP, kinase inhibitor protein; PCNA, proliferating cell nuclear antigen; and TPA, 12-O-tetradecanoylphorbol-13-acetate.)
引用
收藏
页码:453 / 464
页数:12
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