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本文引用的文献

1
EZH2 inhibition as a therapeutic strategy for lymphoma with EZH2-activating mutations.EZH2 抑制作为 EZH2 激活突变淋巴瘤的治疗策略。
Nature. 2012 Dec 6;492(7427):108-12. doi: 10.1038/nature11606. Epub 2012 Oct 10.
2
Development and validation of reagents and assays for EZH2 peptide and nucleosome high-throughput screens.用于EZH2肽和核小体高通量筛选的试剂及检测方法的开发与验证
J Biomol Screen. 2012 Dec;17(10):1279-92. doi: 10.1177/1087057112453765. Epub 2012 Aug 17.
3
Current and emerging treatments in the management of castration-resistant prostate cancer.目前和新兴的治疗方法在去势抵抗性前列腺癌的管理。
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4
ATRA inhibits the proliferation of DU145 prostate cancer cells through reducing the methylation level of HOXB13 gene.维甲酸通过降低 HOXB13 基因的甲基化水平抑制 DU145 前列腺癌细胞的增殖。
PLoS One. 2012;7(7):e40943. doi: 10.1371/journal.pone.0040943. Epub 2012 Jul 13.
5
Polycomb protein EZH2 regulates tumor invasion via the transcriptional repression of the metastasis suppressor RKIP in breast and prostate cancer.多梳蛋白 EZH2 通过转录抑制乳腺癌和前列腺癌中的转移抑制因子 RKIP 来调节肿瘤侵袭。
Cancer Res. 2012 Jun 15;72(12):3091-104. doi: 10.1158/0008-5472.CAN-11-3546. Epub 2012 Apr 13.
6
Loss of let-7 up-regulates EZH2 in prostate cancer consistent with the acquisition of cancer stem cell signatures that are attenuated by BR-DIM.前列腺癌中 let-7 的缺失可上调 EZH2,同时获得癌症干细胞特征,BR-DIM 可减弱这些特征。
PLoS One. 2012;7(3):e33729. doi: 10.1371/journal.pone.0033729. Epub 2012 Mar 19.
7
The role of EZH2 in the regulation of the activity of matrix metalloproteinases in prostate cancer cells.EZH2 在调节前列腺癌细胞基质金属蛋白酶活性中的作用。
PLoS One. 2012;7(1):e30393. doi: 10.1371/journal.pone.0030393. Epub 2012 Jan 17.
8
Cooperation between Polycomb and androgen receptor during oncogenic transformation.多梳抑制复合物和雄激素受体在致癌转化过程中的合作。
Genome Res. 2012 Feb;22(2):322-31. doi: 10.1101/gr.131508.111. Epub 2011 Dec 16.
9
Loading 3-deazaneplanocin A into pegylated unilamellar liposomes by forming transient phenylboronic acid-drug complex and its pharmacokinetic features in Sprague-Dawley rats.通过形成瞬态苯硼酸-药物复合物将 3-去氮氮胞苷载入聚乙二醇化的单层脂质体及其在 Sprague-Dawley 大鼠中的药代动力学特征。
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10
16-hydroxycleroda-3,13-dien-15,16-olide regulates the expression of histone-modifying enzymes PRC2 complex and induces apoptosis in CML K562 cells.16-羟基克氏千里光二萜-15,16-内酯通过调节组蛋白修饰酶 PRC2 复合物的表达诱导 CML K562 细胞凋亡。
Life Sci. 2011 Dec 5;89(23-24):886-95. doi: 10.1016/j.lfs.2011.09.011. Epub 2011 Sep 29.

EZH2,前列腺癌的表观遗传驱动因子。

EZH2, an epigenetic driver of prostate cancer.

机构信息

Division of Hematology/Oncology, Department of Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

出版信息

Protein Cell. 2013 May;4(5):331-41. doi: 10.1007/s13238-013-2093-2. Epub 2013 Apr 30.

DOI:10.1007/s13238-013-2093-2
PMID:23636686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4131440/
Abstract

The histone methyltransferase EZH2 has been in the limelight of the field of cancer epigenetics for a decade now since it was first discovered to exhibit an elevated expression in metastatic prostate cancer. It persists to attract much scientific attention due to its important role in the process of cancer development and its potential of being an effective therapeutic target. Thus here we review the dysregulation of EZH2 in prostate cancer, its function, upstream regulators, downstream effectors, and current status of EZH2-targeting approaches. This review therefore provides a comprehensive overview of EZH2 in the context of prostate cancer.

摘要

组蛋白甲基转移酶 EZH2 自首次发现其在转移性前列腺癌中表达升高以来,已经成为癌症表观遗传学领域的焦点十年。由于其在癌症发展过程中的重要作用及其作为有效治疗靶点的潜力,它仍然吸引着大量的科学关注。因此,我们在这里回顾了 EZH2 在前列腺癌中的失调、它的功能、上游调节剂、下游效应物以及 EZH2 靶向方法的现状。因此,本综述提供了 EZH2 在前列腺癌中的全面概述。