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非编码 RNA 是糖尿病视网膜病变有希望的治疗靶点:最新综述 (2017-2022)。

Noncoding RNAs Are Promising Therapeutic Targets for Diabetic Retinopathy: An Updated Review (2017-2022).

机构信息

Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing 100193, China.

Beijing Key Laboratory of Innovative Drug Discovery of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, Beijing 100193, China.

出版信息

Biomolecules. 2022 Nov 28;12(12):1774. doi: 10.3390/biom12121774.


DOI:10.3390/biom12121774
PMID:36551201
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9775338/
Abstract

Diabetic retinopathy (DR) is the most common complication of diabetes. It is also the main cause of blindness caused by multicellular damage involving retinal endothelial cells, ganglial cells, and pigment epithelial cells in adults worldwide. Currently available drugs for DR do not meet the clinical needs; thus, new therapeutic targets are warranted. Noncoding RNAs (ncRNAs), a new type of biomarkers, have attracted increased attention in recent years owing to their crucial role in the occurrence and development of DR. NcRNAs mainly include microRNAs, long noncoding RNAs, and circular RNAs, all of which regulate gene and protein expression, as well as multiple biological processes in DR. NcRNAs, can regulate the damage caused by various retinal cells; abnormal changes in the aqueous humor, exosomes, blood, tears, and the formation of new blood vessels. This study reviews the different sources of the three ncRNAs-microRNAs, long noncoding RNAs, and circular RNAs-involved in the pathogenesis of DR and the related drug development progress. Overall, this review improves our understanding of the role of ncRNAs in various retinal cells and offers therapeutic directions and targets for DR treatment.

摘要

糖尿病性视网膜病变(DR)是糖尿病最常见的并发症。它也是全世界成年人因涉及视网膜内皮细胞、节细胞和色素上皮细胞的多细胞损伤而导致失明的主要原因。目前用于 DR 的药物不能满足临床需求;因此,需要新的治疗靶点。非编码 RNA(ncRNA)作为一种新型的生物标志物,近年来由于其在 DR 的发生和发展中的关键作用而引起了越来越多的关注。ncRNA 主要包括 microRNAs、长非编码 RNA 和环状 RNA,它们都可以调节基因和蛋白质的表达以及 DR 中的多种生物学过程。ncRNA 可以调节各种视网膜细胞的损伤;房水、外泌体、血液、眼泪中的异常变化以及新血管的形成。本研究综述了参与 DR 发病机制的三种 ncRNA(microRNAs、长非编码 RNA 和环状 RNA)的不同来源及其相关药物开发进展。总的来说,这篇综述提高了我们对 ncRNA 在各种视网膜细胞中的作用的理解,并为 DR 的治疗提供了治疗方向和靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789a/9775338/de48ce3aa7e0/biomolecules-12-01774-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789a/9775338/e9486c52bfc2/biomolecules-12-01774-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789a/9775338/986604c5196d/biomolecules-12-01774-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789a/9775338/95091c42d5ba/biomolecules-12-01774-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789a/9775338/de48ce3aa7e0/biomolecules-12-01774-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789a/9775338/e9486c52bfc2/biomolecules-12-01774-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789a/9775338/986604c5196d/biomolecules-12-01774-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789a/9775338/95091c42d5ba/biomolecules-12-01774-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/789a/9775338/de48ce3aa7e0/biomolecules-12-01774-g004.jpg

相似文献

[1]
Noncoding RNAs Are Promising Therapeutic Targets for Diabetic Retinopathy: An Updated Review (2017-2022).

Biomolecules. 2022-11-28

[2]
miRNA, lncRNA and circRNA: Targeted Molecules Full of Therapeutic Prospects in the Development of Diabetic Retinopathy.

Front Endocrinol (Lausanne). 2021

[3]
Mechanistic and therapeutic perspectives of non-coding RNA-modulated apoptotic signaling in diabetic retinopathy.

Cell Biol Toxicol. 2024-7-6

[4]
Roles of noncoding RNAs in diabetic retinopathy: Mechanisms and therapeutic implications.

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[5]
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[6]
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Mol Cell Biochem. 2024-5

[7]
Research Status of Differentially Expressed Noncoding RNAs in Type 2 Diabetes Patients.

Biomed Res Int. 2020

[8]
Non-coding RNAs and exosomal non-coding RNAs in diabetic retinopathy: A narrative review.

Int J Biol Macromol. 2024-2

[9]
Non-coding RNAs in cardiovascular cell biology and atherosclerosis.

Cardiovasc Res. 2019-10-1

[10]
Emerging Roles of miRNA, lncRNA, circRNA, and Their Cross-Talk in Pituitary Adenoma.

Cells. 2022-9-19

引用本文的文献

[1]
Targeting long non-coding RNA RP11-502I4.3 inhibits the trend of angiogenesis in diabetic retinopathy.

PLoS One. 2025-5-14

[2]
Targeting therapy of PI3K/AKT signaling pathway via non-coding RNAs in diabetic retinopathy.

Naunyn Schmiedebergs Arch Pharmacol. 2025-4-1

[3]
Deciphering the role of exosomal derived regulatory noncoding RNAs as potential biomarkers for diabetic retinopathy: a systematic review.

Int J Retina Vitreous. 2024-12-18

[4]
Identification of genes related to fatty acid metabolism in type 2 diabetes mellitus.

Biochem Biophys Rep. 2024-10-22

[5]
Classical and Innovative Evidence for Therapeutic Strategies in Retinal Dysfunctions.

Int J Mol Sci. 2024-2-9

[6]
Exosomal noncoding RNA: A potential therapy for retinal vascular diseases.

Mol Ther Nucleic Acids. 2024-1-24

[7]
Relationship between Biochemical Pathways and Non-Coding RNAs Involved in the Progression of Diabetic Retinopathy.

J Clin Med. 2024-1-4

本文引用的文献

[1]
Reducing Akt2 in retinal pigment epithelial cells causes a compensatory increase in Akt1 and attenuates diabetic retinopathy.

Nat Commun. 2022-10-13

[2]
LncRNA FLG-AS1 Mitigates Diabetic Retinopathy by Regulating Retinal Epithelial Cell Inflammation, Oxidative Stress, and Apoptosis via miR-380-3p/SOCS6 Axis.

Inflammation. 2022-10

[3]
High level of lncRNA NR2F1-AS1 predict the onset and progression of diabetic retinopathy in type 2 diabetes.

Exp Eye Res. 2022-6

[4]
Danhong injection represses diabetic retinopathy and nephropathy advancement in diabetic mice by upregulating microRNA-30d-5p and targeting JAK1.

Bioengineered. 2022-4

[5]
Müller glia-derived exosomal miR-9-3p promotes angiogenesis by restricting sphingosine-1-phosphate receptor S1P in diabetic retinopathy.

Mol Ther Nucleic Acids. 2021-12-17

[6]
miR-125a-5p attenuates macrophage-mediated vascular dysfunction by targeting Ninjurin1.

Cell Death Differ. 2022-6

[7]
MiR-423-5p activated by E2F1 promotes neovascularization in diabetic retinopathy by targeting HIPK2.

Diabetol Metab Syndr. 2021-12-28

[8]
The Aflibercept-Induced MicroRNA Profile in the Vitreous of Proliferative Diabetic Retinopathy Patients Detected by Next-Generation Sequencing.

Front Pharmacol. 2021-12-6

[9]
Downregulation of Circular RNA PSEN1 ameliorates ferroptosis of the high glucose treated retinal pigment epithelial cells via miR-200b-3p/cofilin-2 axis.

Bioengineered. 2021-12

[10]
miRNA, lncRNA and circRNA: Targeted Molecules Full of Therapeutic Prospects in the Development of Diabetic Retinopathy.

Front Endocrinol (Lausanne). 2021

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