The DOI matches its Crossref record; 101 of the 101 references it cites were found in a registry or an index.
Ocular neovascularization
Open accessAbstract
Retinal and choroidal vascular diseases constitute the most common causes of moderate and severe vision loss in developed countries. They can be divided into retinal vascular diseases, in which there is leakage and/or neovascularization (NV) from retinal vessels, and subretinal NV, in which new vessels grow into the normally avascular outer retina and subretinal space. The first category of diseases includes diabetic retinopathy, retinal vein occlusions, and retinopathy of prematurity, and the second category includes neovascular age-related macular degeneration (AMD), ocular histoplasmosis, pathologic myopia, and other related diseases. Retinal hypoxia is a key feature of the first category of diseases resulting in elevated levels of hypoxia-inducible factor-1 (HIF-1) which stimulates expression of vascular endothelial growth factor (VEGF), platelet-derived growth factor-B (PDGF-B), placental growth factor, stromal-derived growth factor-1 and their receptors, as well as other hypoxia-regulated gene products such as angiopoietin-2. Although hypoxia has not been demonstrated as part of the second category of diseases, HIF-1 is elevated and thus the same group of hypoxia-regulated gene products plays a role. Clinical trials have shown that VEGF antagonists provide major benefits for patients with subretinal NV due to AMD and even greater benefits are seen by combining antagonists of VEGF and PDGF-B. It is likely that addition of antagonists of other agents listed above will be tested in the future. Other appealing strategies are to directly target HIF-1 or to use gene transfer to express endogenous or engineered anti-angiogenic proteins. While substantial progress has been made, the future looks even brighter for patients with retinal and choroidal vascular diseases.
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Ranibizumab for Neovascular Age-Related Macular Degeneration
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Vascular endothelial growth factor induced by hypoxia may mediate hypoxia-initiated angiogenesis
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Self-Healing Injectable Hydrogels for Tissue Regeneration
Bertsch, P., Diba, M., Mooney, D. J., & Leeuwenburgh, S. C. G. (2023) · Chemical Reviews · doi:10.1021/acs.chemrev.2c00179 · Cited by 892
Targeting hypoxia-inducible factors: therapeutic opportunities and challenges
Yuan, X., Ruan, W., Bobrow, B., Carmeliet, P., & Eltzschig, H. K. (2024) · Nature Reviews Drug Discovery · doi:10.1038/s41573-023-00848-6 · Cited by 245
Hypoxia-inducible factor-1α: A promising therapeutic target for vasculopathy in diabetic retinopathy
Li, H.-Y., Yuan, Y., Fu, Y.-H., Wang, Y., & Gao, X.-Y. (2020) · Pharmacological Research · doi:10.1016/j.phrs.2020.104924 · Cited by 88
Gene Therapy Intervention in Neovascular Eye Disease: A Recent Update
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Maugeri, G., Bucolo, C., Drago, F., Rossi, S., Di Rosa, M., Imbesi, R., D’Agata, V., & Giunta, S. (2021) · Frontiers in Pharmacology · doi:10.3389/fphar.2021.684680 · Cited by 47
“The expression of VEGF by RPE cells has been analyzed in different studies, and the results have contributed to our knowledge on the involvement RPE cells in the pathophysiology of DR (Saishin et al., 2003; Campochiaro, 2013).”
Result
Metadata
- Authors
- Campochiaro, P. A.
- Venue
- Journal of Molecular Medicine
- Published
- 2013-01-18
- Volume
- 91
- Issue
- 3
- Pages
- 311-321
- ISSN
- 0946-2716 (ISSN-L)
- 1432-1440
- OpenAlex
- W4232181833
- Cited by
- 386
- References
- 101
- FWCI
- 27.41
- Type
- journal article
- Language
- en
- Open access
- green
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