Cai Chunyang, Meng Chunren, He Shuai, Gu Chufeng, Lhamo Thashi, Draga Deji, Luo Dawei, Qiu Qinghua
Department of Ophthalmology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, People's Republic of China.
National Clinical Research Center for Eye Diseases, Shanghai Key Laboratory of Ocular Fundus Diseases, Shanghai Engineering Center for Visual Science and Photomedicine, Shanghai Engineering Center for Precise Diagnosis and Treatment of Eye Diseases, Shanghai, People's Republic of China.
Cell Biosci. 2022 Nov 17;12(1):186. doi: 10.1186/s13578-022-00927-y.
Diabetic retinopathy (DR), a specific neuron-vascular complication of diabetes, is a major cause of vision loss among middle-aged people worldwide, and the number of DR patients will increase with the increasing incidence of diabetes. At present, it is limited in difficult detection in the early stages, limited treatment and unsatisfactory treatment effects in the advanced stages.
The pathogenesis of DR is complicated and involves epigenetic modifications, oxidative stress, inflammation and neovascularization. These factors influence each other and jointly promote the development of DR. DNA methylation is the most studied epigenetic modification, which has been a key role in the regulation of gene expression and the occurrence and development of DR. Thus, this review investigates the relationship between DNA methylation and other complex pathological processes in the development of DR. From the perspective of DNA methylation, this review provides basic insights into potential biomarkers for diagnosis, preventable risk factors, and novel targets for treatment.
DNA methylation plays an indispensable role in DR and may serve as a prospective biomarker of this blinding disease in its relatively early stages. In combination with inhibitors of DNA methyltransferases can be a potential approach to delay or even prevent patients from getting advanced stages of DR.
糖尿病视网膜病变(DR)是糖尿病一种特定的神经血管并发症,是全球中年人视力丧失的主要原因,且随着糖尿病发病率的上升,DR患者数量也会增加。目前,其在早期难以检测,在晚期治疗手段有限且治疗效果不理想。
DR的发病机制复杂,涉及表观遗传修饰、氧化应激、炎症和新生血管形成。这些因素相互影响,共同促进DR的发展。DNA甲基化是研究最多的表观遗传修饰,在基因表达调控以及DR的发生发展中起关键作用。因此,本综述探讨DNA甲基化与DR发展中其他复杂病理过程之间的关系。从DNA甲基化的角度,本综述为潜在的诊断生物标志物、可预防的危险因素及新的治疗靶点提供了基本见解。
DNA甲基化在DR中起不可或缺的作用,可能作为这种致盲疾病相对早期阶段的一种前瞻性生物标志物。联合DNA甲基转移酶抑制剂可能是延缓甚至预防患者进入DR晚期阶段的一种潜在方法。