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[DNA损伤反应中p53的研究进展]

[Advances in the study of p53 in response to DNA damage].

作者信息

Wang Ya-Jie, Sun Hua, Liu Geng-Tao, Chen Xiao-Guang

机构信息

Institute of Materia Medica, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing 100050, China.

出版信息

Yao Xue Xue Bao. 2011 Dec;46(12):1413-9.

PMID:22375412
Abstract

p53 (encoded by TP53) is undoubtedly one of the most extensively studied genes and proteins. It is a highly potent transcription factor which, under normal circumstances, is maintained at low level. Both genotoxic and non-genotoxic stresses can induce p53 stabilized leading to changes in the expression of p53-responsive genes. The biological outcome inducing this pathway can be either growth arrest and apoptosis or senescence to maintain the integrity of the genome or to delete the damaged cells. The biochemical activity of p53 itself and the cellular environment govern the choice between these outcomes in a cell type- and stress-specific manner. So, p53 is a pivotal tumour suppressor and a mainstay of our body's natural anticancer defence. This review could provide some useful information for further study on the mechanisms of tumorigenesis and its progression, and also could contribute to the discovery of antitumor agents.

摘要

p53(由TP53编码)无疑是研究最为广泛的基因和蛋白质之一。它是一种高效的转录因子,在正常情况下维持在低水平。基因毒性和非基因毒性应激均可诱导p53稳定,导致p53反应性基因表达发生变化。诱导该途径的生物学结果可以是生长停滞、凋亡或衰老,以维持基因组的完整性或清除受损细胞。p53自身的生化活性和细胞环境以细胞类型和应激特异性方式决定这些结果之间的选择。因此,p53是关键的肿瘤抑制因子,也是人体天然抗癌防御的中流砥柱。本综述可为进一步研究肿瘤发生及其进展机制提供一些有用信息,也有助于发现抗肿瘤药物。

相似文献

1
[Advances in the study of p53 in response to DNA damage].[DNA损伤反应中p53的研究进展]
Yao Xue Xue Bao. 2011 Dec;46(12):1413-9.
2
The p53 response to DNA damage.p53对DNA损伤的反应。
DNA Repair (Amst). 2004 Aug-Sep;3(8-9):1049-56. doi: 10.1016/j.dnarep.2004.03.027.
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UBTD1 induces cellular senescence through an UBTD1-Mdm2/p53 positive feedback loop.UBTD1通过UBTD1-Mdm2/p53正反馈环诱导细胞衰老。
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Death squads enlisted by the tumour suppressor p53.由肿瘤抑制因子p53招募的死亡小队。
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Regulation of p53 by hypoxia: dissociation of transcriptional repression and apoptosis from p53-dependent transactivation.缺氧对p53的调控:转录抑制及凋亡与p53依赖性反式激活的解离
Mol Cell Biol. 2001 Feb;21(4):1297-310. doi: 10.1128/MCB.21.4.1297-1310.2001.
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Activation and activities of the p53 tumour suppressor protein.p53肿瘤抑制蛋白的激活与活性
Br J Cancer. 2001 Dec 14;85(12):1813-23. doi: 10.1054/bjoc.2001.2128.
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Indole-3-carbinol activates the ATM signaling pathway independent of DNA damage to stabilize p53 and induce G1 arrest of human mammary epithelial cells.吲哚 - 3 - 甲醇可独立于DNA损伤激活ATM信号通路,以稳定p53并诱导人乳腺上皮细胞的G1期阻滞。
Int J Cancer. 2006 Feb 15;118(4):857-68. doi: 10.1002/ijc.21445.
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Restoration of p53 pathway by nutlin-3 induces cell cycle arrest and apoptosis in human rhabdomyosarcoma cells.Nutlin-3恢复p53信号通路可诱导人横纹肌肉瘤细胞的细胞周期停滞和凋亡。
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The p53 tumor suppressor protein is a critical regulator of hematopoietic stem cell behavior.p53 肿瘤抑制蛋白是造血干细胞行为的关键调节因子。
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The p53 mRNA-Mdm2 interaction controls Mdm2 nuclear trafficking and is required for p53 activation following DNA damage.p53mRNA-Mdm2 相互作用控制 Mdm2 的核转运,并且是 DNA 损伤后 p53 激活所必需的。
Cancer Cell. 2012 Jan 17;21(1):25-35. doi: 10.1016/j.ccr.2011.11.016.

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