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表观遗传学与常见眼科疾病

Epigenetics and Common Ophthalmic Diseases.

作者信息

Li Wendy, Liu Ji, Galvin Jennifer A

机构信息

Department of Ophthalmology and Visual Science, Yale School of Medicine, New Haven, CT.

出版信息

Yale J Biol Med. 2016 Dec 23;89(4):597-600. eCollection 2016 Dec.

PMID:28018148
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5168835/
Abstract

The study of ocular diseases and epigenetic dysregulation is an emerging area of research. The knowledge from the epigenetic mechanisms of DNA methylation, histone modifications, chromatin remodeling, and non-coding RNAs regarding the pathogenesis of ocular diseases will be helpful for improved treatment modalities for our patients. In particular, we focus upon the how epigenetic regulatory mechanisms impact five common ocular diseases: age related macular degeneration, age-related cataract, pterygium, retinoblastoma, and uveal melanoma. Hence, the foundation of this research paves the way for future specific therapeutic targets to treat and prevent vision loss.

摘要

眼部疾病与表观遗传失调的研究是一个新兴的研究领域。从DNA甲基化、组蛋白修饰、染色质重塑和非编码RNA的表观遗传机制中获得的关于眼部疾病发病机制的知识,将有助于改善我们对患者的治疗方式。特别是,我们关注表观遗传调控机制如何影响五种常见的眼部疾病:年龄相关性黄斑变性、年龄相关性白内障、翼状胬肉、视网膜母细胞瘤和葡萄膜黑色素瘤。因此,这项研究的基础为未来治疗和预防视力丧失的特定治疗靶点铺平了道路。

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本文引用的文献

1
Epigenetics and ocular diseases: from basic biology to clinical study.表观遗传学与眼病:从基础生物学到临床研究。
J Cell Physiol. 2014 Jul;229(7):825-33. doi: 10.1002/jcp.24522.
2
Epigenetics in ocular diseases.眼疾的表观遗传学。
Curr Genomics. 2013 May;14(3):166-72. doi: 10.2174/1389202911314030002.
3
Correlation between microRNA-34a levels and lens opacity severity in age-related cataracts.miRNA-34a 水平与年龄相关性白内障晶状体混浊严重程度的相关性。
Eye (Lond). 2013 Jul;27(7):883-8. doi: 10.1038/eye.2013.90. Epub 2013 May 10.
4
MiR-365b-3p, down-regulated in retinoblastoma, regulates cell cycle progression and apoptosis of human retinoblastoma cells by targeting PAX6.miR-365b-3p 在视网膜母细胞瘤中下调,通过靶向 PAX6 调节人视网膜母细胞瘤细胞的细胞周期进程和细胞凋亡。
FEBS Lett. 2013 Jun 19;587(12):1779-86. doi: 10.1016/j.febslet.2013.04.029. Epub 2013 May 6.
5
Hypomethylation of the IL17RC promoter associates with age-related macular degeneration.IL17RC 启动子的低甲基化与年龄相关性黄斑变性有关。
Cell Rep. 2012 Nov 29;2(5):1151-8. doi: 10.1016/j.celrep.2012.10.013. Epub 2012 Nov 21.
6
5-Methylcytosine DNA demethylation: more than losing a methyl group.5- 甲基胞嘧啶 DNA 去甲基化:不只是失去一个甲基。
Annu Rev Genet. 2012;46:419-41. doi: 10.1146/annurev-genet-110711-155451. Epub 2012 Sep 4.
7
Down-regulation and CpG island hypermethylation of CRYAA in age-related nuclear cataract.CRYAA 在年龄相关性核性白内障中的下调和 CpG 岛甲基化。
FASEB J. 2012 Dec;26(12):4897-902. doi: 10.1096/fj.12-213702. Epub 2012 Aug 13.
8
DNA methylation is associated with altered gene expression in AMD.DNA 甲基化与 AMD 中基因表达的改变有关。
Invest Ophthalmol Vis Sci. 2012 Apr 24;53(4):2089-105. doi: 10.1167/iovs.11-8449.
9
Chromatin replication and epigenome maintenance.染色质复制和表观基因组维护。
Nat Rev Mol Cell Biol. 2012 Feb 23;13(3):153-67. doi: 10.1038/nrm3288.
10
Epigenetic and copy number variation analysis in retinoblastoma by MS-MLPA.应用 MS-MLPA 技术对视网膜母细胞瘤进行表观遗传学和拷贝数变异分析。
Pathol Oncol Res. 2012 Jul;18(3):703-12. doi: 10.1007/s12253-012-9498-8. Epub 2012 Jan 26.