生物
细胞周期
细胞生物学
细胞周期蛋白依赖激酶
增殖细胞核抗原
DNA损伤
细胞周期检查点
DNA修复
支票1
限制点
细胞凋亡
转录因子
DNA
癌症研究
基因
遗传学
作者
Ansar Karimian,Yasin Ahmadi,Bahman Yousefi
出处
期刊:DNA Repair
[Elsevier BV]
日期:2016-04-30
卷期号:42: 63-71
被引量:928
标识
DOI:10.1016/j.dnarep.2016.04.008
摘要
An appropriate control over cell cycle progression depends on many factors. Cyclin-dependent kinase (CDK) inhibitor p21 (also known as p21(WAF1/Cip1)) is one of these factors that promote cell cycle arrest in response to a variety of stimuli. The inhibitory effect of P21 on cell cycle progression correlates with its nuclear localization. P21 can be induced by both p53-dependent and p53-independent mechanisms. Some other important functions attributed to p21 include transcriptional regulation, modulation or inhibition of apoptosis. These functions are largely dependent on direct p21/protein interactions and also on p21 subcellular localizations. In addition, p21 can play a role in DNA repair by interacting with proliferating cell nuclear antigen (PCNA). In this review, we will focus on the multiple functions of p21 in cell cycle regulation, apoptosis and gene transcription after DNA damage and briefly discuss the pathways and factors that have critical roles in p21 expression and activity.
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