Rho-Kinase/ROCK as a Potential Drug Target for Vitreoretinal Diseases.
Muneo YamaguchiShintaro NakaoMitsuru ArimaIori WadaYoshihiro KaizuFeng HaoShigeo YoshidaKoh-Hei SonodaPublished in: Journal of ophthalmology (2017)
Rho-associated kinase (Rho-kinase/ROCK) was originally identified as an effector protein of the G protein Rho. Its involvement in various diseases, particularly cancer and cardiovascular disease, has been elucidated, and ROCK inhibitors have already been applied clinically for cerebral vasospasm and glaucoma. Vitreoretinal diseases including diabetic retinopathy, age-related macular degeneration, and proliferative vitreoretinoapthy are still a major cause of blindness. While anti-VEGF therapy has recently been widely used for vitreoretinal disorders due to its efficacy, attention has been drawn to new unmet needs. The importance of ROCK in pathological vitreoretinal conditions has also been elucidated and is attracting attention as a potential therapeutic target. ROCK is involved in angiogenesis and hyperpermeability and also in the pathogenesis of various pathologies such as inflammation and fibrosis. It has been expected that ROCK inhibitors will become new molecular target drugs for vitreoretinal diseases. This review summarizes the recent progress on the mechanisms of action of ROCK and their applications in disease treatment.
Keyphrases
- protein kinase
- diabetic retinopathy
- cardiovascular disease
- age related macular degeneration
- subarachnoid hemorrhage
- working memory
- smooth muscle
- oxidative stress
- type diabetes
- tyrosine kinase
- endothelial cells
- squamous cell carcinoma
- stem cells
- regulatory t cells
- metabolic syndrome
- cardiovascular events
- dendritic cells
- risk assessment
- mesenchymal stem cells
- small molecule
- binding protein
- smoking cessation
- optic nerve
- cardiovascular risk factors