miRNAs as potential therapeutic targets for age-related macular degeneration
Open accessAbstract
Since their recent discovery, miRNAs have been shown to play critical roles in a variety of pathophysiological processes. Such processes include pathological angiogenesis, the oxidative stress response, immune response and inflammation, all of which have been shown to have important and interdependent roles in the pathogenesis and progression of age-related macular degeneration (AMD). Here we present a brief review of the pathological processes involved in AMD and review miRNAs and other noncoding RNAs involved in regulating these processes. Specifically, we discuss several candidate miRNAs that show promise as AMD therapeutic targets due to their direct involvement in choroidal neovascularization or retinal pigment epithelium atrophy. We discuss potential miRNA-based therapeutics and delivery methods for AMD and provide future directions for the field of miRNA research with respect to AMD. We believe the future of miRNAs in AMD therapy is promising.
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Gene Therapy for Retinal Degenerative Diseases: Progress, Challenges, and Future Directions
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- Authors
- Wang, S., Koster, K. M., He, Y., & Zhou, Q.
- Affiliations
- The University of Texas Southwestern Medical Center (US)
- Department of Ophthalmology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX75390, USA
- Corresponding author
- Wang, Shusheng
- Venue
- Future Medicinal Chemistry
- Publisher
- Informa UK Limited
- Published
- 2012-03
- Volume
- 4
- Issue
- 3
- Pages
- 277-287
- ISSN
- 1756-8919 (ISSN-L)
- 1756-8927
- PMC
- PMC3313592
- OpenAlex
- W2151225614
- Cited by
- 67
- References
- 110
- Citations by year
- 2026: 3 · 2025: 2 · 2024: 2 · 2023: 2 · 2022: 4 · 2021: 5 · 2020: 8 · 2019: 5 · 2018: 7 · 2017: 7 · 2016: 7 · 2015: 6 · 2014: 6 · 2013: 2 · 2012: 1
- FWCI
- 0.74
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Future Medicinal Chemistry (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- UT Southwestern Medical Center (EY021862 and EY020799)
- Topics
- Health Sciences › Medicine › Ophthalmology › Retinal Diseases and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › MicroRNA in disease regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinal Development and Disorders
- Keywords
- microRNA, age-related macular degeneration, therapeutic target, choroidal neovascularization, retinal pigment epithelium atrophy, pathological angiogenesis, oxidative stress, inflammation, non-coding RNA, miRNA-based therapy, microRNA delivery
- MeSH terms
- Animals, Humans, Inflammation, Macula Lutea, Macular Degeneration, Oxidative Stress, Choroidal Neovascularization, MicroRNAs, Drug Discovery
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
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