Multiple functions of p21 in cell cycle, apoptosis and transcriptional regulation after DNA damage

被引:871
作者
Karimian, Ansar [1 ,2 ,3 ]
Ahmadi, Yasin [2 ,3 ]
Yousefi, Bahman [2 ,3 ,4 ]
机构
[1] Tabriz Univ Med Sci, Immunol Res Ctr, Tabriz, Iran
[2] Tabriz Univ Med Sci, Fac Med, Dept Clin Biochem & Lab Med, Tabriz, Iran
[3] Tabriz Univ Med Sci, Student Res Comm, Tabriz, Iran
[4] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
关键词
Apoptosis; Cell cycle; DNA damage; p21; TUMOR-SUPPRESSOR GENE; PROTEIN-KINASE B/AKT; SIGNALING PATHWAY; ARSENIC TRIOXIDE; DIFFERENTIAL REGULATION; P21(WAF1/CIP1) EXPRESSION; HUMAN FIBROBLASTS; SELENOPROTEIN-W; CANCER-CELLS; TARGET GENE;
D O I
10.1016/j.dnarep.2016.04.008
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
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. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 71
页数:9
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