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环状RNA在糖尿病视网膜病变中的新兴作用

Emerging role of circular RNAs in diabetic retinopathy.

作者信息

Kim Hyunjong, Ryu Juhee

机构信息

Vessel-Organ Interaction Research Center, College of Pharmacy, Kyungpook National University, Daegu 41566, Korea.

College of Pharmacy and Research Institute of Pharmaceutical Sciences, Kyungpook National University, Daegu 41566, Korea.

出版信息

Korean J Physiol Pharmacol. 2025 Jul 1;29(4):385-397. doi: 10.4196/kjpp.24.389. Epub 2025 May 15.

DOI:10.4196/kjpp.24.389
PMID:40368849
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12198446/
Abstract

Diabetic retinopathy (DR), a significant complication that affects the retina of individuals with diabetes, poses a severe threat to their visual health. DR is classified into stages ranging from non-proliferative to proliferative forms. As the disease progresses, pathological neovascularization and hemorrhage in the retina or vitreous can occur, potentially leading to vision impairment or blindness. Current treatments for DR include intravitreal injections of anti-vascular endothelial growth factor drugs and surgical interventions such as laser photocoagulation. However, these treatments are associated with various complications and side effects. Therefore, cellular and epigenetic studies are necessary to better understand the pathogenesis of DR, which may lead to the development of novel therapeutic strategies. Several studies have demonstrated the role of circular RNAs (circRNAs) in the pathogenesis and progression of DR. CircRNAs have been shown to regulate the expression of genes involved in the proliferation, differentiation, or angiogenesis of different retinal cells, thereby influencing their function. Therefore, this review aims to investigate the role of circRNAs in different retinal cell types in DR and evaluate their potential as diagnostic and therapeutic targets for the disease.

摘要

糖尿病性视网膜病变(DR)是一种影响糖尿病患者视网膜的严重并发症,对其视觉健康构成严重威胁。DR分为从非增殖性到增殖性的不同阶段。随着疾病进展,视网膜或玻璃体中可出现病理性新生血管形成和出血,可能导致视力损害或失明。DR的当前治疗方法包括玻璃体内注射抗血管内皮生长因子药物以及激光光凝等手术干预。然而,这些治疗与各种并发症和副作用相关。因此,细胞和表观遗传学研究对于更好地理解DR的发病机制是必要的,这可能会导致新治疗策略的开发。多项研究已证明环状RNA(circRNA)在DR的发病机制和进展中的作用。CircRNA已被证明可调节参与不同视网膜细胞增殖、分化或血管生成的基因表达,从而影响其功能。因此,本综述旨在研究circRNA在DR不同视网膜细胞类型中的作用,并评估它们作为该疾病诊断和治疗靶点的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9705/12198446/8a8001b9a6a0/kjpp-29-4-385-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9705/12198446/3765445423f0/kjpp-29-4-385-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9705/12198446/8a8001b9a6a0/kjpp-29-4-385-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9705/12198446/3765445423f0/kjpp-29-4-385-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9705/12198446/8a8001b9a6a0/kjpp-29-4-385-f2.jpg

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本文引用的文献

1
Systematic identification and characterization of exon-intron circRNAs.外显子-内含子环状RNA的系统鉴定与表征
Genome Res. 2024 Apr 25;34(3):376-393. doi: 10.1101/gr.278590.123.
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Encapsulation and assessment of therapeutic cargo in engineered exosomes: a systematic review.工程化外泌体中治疗性货物的包封和评估:系统评价。
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eIF4A3-mediated circEHMT1 regulation in retinal microvascular endothelial dysfunction in diabetic retinopathy.eIF4A3 介导的环状 EHMT1 在糖尿病性视网膜病变中的视网膜微血管内皮功能障碍中的调控作用。
Microvasc Res. 2024 Jan;151:104612. doi: 10.1016/j.mvr.2023.104612. Epub 2023 Oct 13.
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Targeting materials and strategies for RNA delivery.靶向 RNA 递送的材料和策略。
Theranostics. 2023 Aug 21;13(13):4667-4693. doi: 10.7150/thno.87316. eCollection 2023.
5
The hsa_circ_0004805/hsa_miR-149-5p/TGFB2 axis plays critical roles in the pathophysiology of diabetic retinopathy in vitro and in vivo.hsa_circ_0004805/hsa_miR-149-5p/TGFB2 轴在糖尿病视网膜病变的体外和体内病理生理学中发挥关键作用。
Mol Cell Endocrinol. 2023 Oct 1;576:112042. doi: 10.1016/j.mce.2023.112042. Epub 2023 Aug 10.
6
The circRNA MKLN1 regulates autophagy in the development of diabetic retinopathy.环状 RNA MKLN1 在糖尿病性视网膜病变的发展过程中调控自噬。
Biochim Biophys Acta Mol Basis Dis. 2023 Dec;1869(8):166839. doi: 10.1016/j.bbadis.2023.166839. Epub 2023 Aug 6.
7
Prevalence of diabetic retinopathy and vision-threatening diabetic retinopathy in adults with diabetes in China.中国成人糖尿病患者中糖尿病视网膜病变及威胁视力的糖尿病视网膜病变的患病率。
Nat Commun. 2023 Jul 18;14(1):4296. doi: 10.1038/s41467-023-39864-w.
8
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Commun Biol. 2023 Jul 13;6(1):719. doi: 10.1038/s42003-023-05064-x.
9
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