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组蛋白去乙酰化酶对细胞周期调节因子的调控

Modulation of cell cycle regulators by HDACs.

作者信息

Telles Elphine, Seto Edward

机构信息

Department of Molecular Oncology, H Lee Moffitt Cancer Center and Research Institute, Tampa, FL 33612, USA.

出版信息

Front Biosci (Schol Ed). 2012 Jan 1;4(3):831-9. doi: 10.2741/s303.

DOI:10.2741/s303
PMID:22202094
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3990255/
Abstract

Histone deacetylases (HDACs) catalyze the deacetylation of lysine residues on histones and non-histone proteins. HDACs have been shown to control the functions of key cell cycle proteins. Consistent with this, the overexpression of HDACs has been observed in multiple cancers, resulting in deregulation of the cell cycle and uncontrolled proliferation. This review focuses on the impact that HDACs have on cell cycle control through the deacetylation of proteins.

摘要

组蛋白脱乙酰酶(HDACs)催化组蛋白和非组蛋白上赖氨酸残基的脱乙酰化反应。研究表明,HDACs可调控关键细胞周期蛋白的功能。与此相符的是,在多种癌症中均观察到HDACs的过表达,这导致细胞周期失调和细胞增殖失控。本综述聚焦于HDACs通过蛋白质脱乙酰化作用对细胞周期调控的影响。

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本文引用的文献

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J Biomed Biotechnol. 2011;2011:371832. doi: 10.1155/2011/371832. Epub 2010 Dec 5.
2
The clinical development of histone deacetylase inhibitors as targeted anticancer drugs.组蛋白去乙酰化酶抑制剂作为靶向抗癌药物的临床开发。
Expert Opin Investig Drugs. 2010 Sep;19(9):1049-66. doi: 10.1517/13543784.2010.510514.
3
Overlapping functions of Hdac1 and Hdac2 in cell cycle regulation and haematopoiesis.Hdac1 和 Hdac2 在细胞周期调控和造血中的重叠功能。
EMBO J. 2010 Aug 4;29(15):2586-97. doi: 10.1038/emboj.2010.136. Epub 2010 Jun 22.
4
p53-induced growth arrest is regulated by the mitochondrial SirT3 deacetylase.p53 诱导的生长停滞受线粒体 SirT3 去乙酰化酶的调节。
PLoS One. 2010 May 5;5(5):e10486. doi: 10.1371/journal.pone.0010486.
5
Aging and disease: connections to sirtuins.衰老与疾病:与 Sirtuins 的关联。
Aging Cell. 2010 Apr;9(2):285-90. doi: 10.1111/j.1474-9726.2010.00548.x.
6
Histone deacetylase 7 controls endothelial cell growth through modulation of beta-catenin.组蛋白去乙酰化酶 7 通过调节β-连环蛋白控制血管内皮细胞的生长。
Circ Res. 2010 Apr 16;106(7):1202-11. doi: 10.1161/CIRCRESAHA.109.213165. Epub 2010 Mar 11.
7
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Mol Cell Biol. 2010 Mar;30(5):1171-81. doi: 10.1128/MCB.01500-09. Epub 2009 Dec 22.
8
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9
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Lysine acetylation targets protein complexes and co-regulates major cellular functions.赖氨酸乙酰化作用于蛋白质复合物,并共同调节主要的细胞功能。
Science. 2009 Aug 14;325(5942):834-40. doi: 10.1126/science.1175371. Epub 2009 Jul 16.