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CircRNA in ocular neovascular diseases: Fundamental mechanism and clinical potential.
- Source :
-
Pharmacological Research . Nov2023, Vol. 197, pN.PAG-N.PAG. 1p. - Publication Year :
- 2023
-
Abstract
- Ocular neovascular disease (OND), characterized by the aberrant formation of immature blood vessels, is the leading cause of vision impairment and blindness. It is important to find effective ways to diagnose and treat these diseases. Circular RNA (circRNA) is a group of endogenous non-coding RNA that play a crucial role in regulating different biological processes. Due to their close association with ocular disease and angiogenesis, circRNAs have become a hotspot in OND research. In this review, we intensively investigate the possibility of using circRNAs in the management of ONDs. In general, angiogenesis is divided into five phases. On the basis of these five steps, we describe the potential of using circRNAs by introducing how they regulate angiogenesis. Subsequently, the interactions between circRNAs and ONDs, including pterygium, corneal neovascularization, age-related macular degeneration, diabetic retinopathy, and retinopathy of prematurity, are analyzed in detail. We also introduce the potential use of circRNAs as OND diagnostic biomarkers. Finally, we summarize the prospects of using circRNAs as a potential strategy in OND management. The gaps in recent research are also pointed out with the purpose of promoting the introduction of circRNAs into clinical applications. [Display omitted] ● CircRNA influences neovascularization by regulating the five phases of angiogenesis. ● CircRNA affects ocular neovascular diseases mainly by regulating neovascularization. ● CircRNA is promising for diagnosis and treatment of ocular neovascular diseases. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 10436618
- Volume :
- 197
- Database :
- Academic Search Index
- Journal :
- Pharmacological Research
- Publication Type :
- Academic Journal
- Accession number :
- 173701273
- Full Text :
- https://doi.org/10.1016/j.phrs.2023.106946