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表观遗传学与退行性视网膜疾病:新治疗方法的前景。

Epigenetics and Degenerative Retinal Diseases: Prospects for New Therapeutic Approaches.

机构信息

Department of Neural and Behavioral Sciences, Penn State College of Medicine, PA, US.

出版信息

Asia Pac J Ophthalmol (Phila). 2022;11(4):328-334. doi: 10.1097/APO.0000000000000520. Epub 2022 Aug 30.

DOI:10.1097/APO.0000000000000520
PMID:36041147
Abstract

There is growing evidence that retinal degenerative diseases are accompanied by epigenetic changes in both deoxyribonucleic acid methylation and histone modification. Even in the monogenic disease retinitis pigmentosa, there is a cascade of changes in gene expression that correlate with epigenetic changes, suggesting that many of the symptoms, and degenerative changes, may be a result of epigenetic changes downstream from the genetic mutation. This is supported by data from studies of diabetic retinopathy and macular degeneration, 2 diseases where it has been difficult to define a single causative change. Initial studies with modifiers of deoxyribonucleic acid methylation suggest that they can provide therapeutic benefit. A number of drugs are available to inhibit specific epigenetic histone modifier enzymes, and these offer the possibility of new therapeutic approaches to retinal disease. Systemic treatment with inhibitors of histone demethylases and histone deacetylases have arrested rod degeneration in rodent models of retinitis pigmentosa. Some evidence has suggested that similar treatments may provide benefits for patients with diabetic retinopathy. Because differentiation of retinal stem cells is regulated in part by epigenetic mechanisms, it may also be possible to direct stem cell differentiation pathways through the use of selective epigenetic modifiers. This is predicted to provide a valuable avenue to accelerate the introduction of regenerative approaches to retinal disease. Epigenetic modifiers are poised to become a powerful new approach to treat retinal degenerative diseases.

摘要

越来越多的证据表明,视网膜退行性疾病伴随着脱氧核糖核酸甲基化和组蛋白修饰的表观遗传变化。即使在单基因疾病色素性视网膜炎中,也存在一系列与表观遗传变化相关的基因表达变化,这表明许多症状和退行性变化可能是基因突变下游的表观遗传变化的结果。这一观点得到了来自糖尿病性视网膜病变和黄斑变性研究的数据的支持,这两种疾病很难确定单一的致病变化。对脱氧核糖核酸甲基化修饰剂的初步研究表明,它们可以提供治疗益处。有许多药物可用于抑制特定的表观遗传组蛋白修饰酶,这为视网膜疾病的新治疗方法提供了可能性。用组蛋白脱甲基酶和组蛋白去乙酰化酶的抑制剂进行全身治疗已经阻止了色素性视网膜炎的啮齿动物模型中的杆状细胞退化。一些证据表明,类似的治疗可能对糖尿病性视网膜病变患者有益。由于视网膜干细胞的分化部分受表观遗传机制的调节,因此也可以通过使用选择性的表观遗传修饰剂来指导干细胞分化途径。这有望为加速引入视网膜疾病的再生方法提供一条有价值的途径。表观遗传修饰剂有望成为治疗视网膜退行性疾病的一种强大的新方法。

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