Novel Programmed Cell Death as Therapeutic Targets in Age-Related Macular Degeneration?
Ming YangKwok-Fai SoWai Ching LamAmy Cheuk Yin LoPublished in: International journal of molecular sciences (2020)
Age-related macular degeneration (AMD) is a leading cause of severe visual loss among the elderly. AMD patients are tormented by progressive central blurring/loss of vision and have limited therapeutic options to date. Drusen accumulation causing retinal pigment epithelial (RPE) cell damage is the hallmark of AMD pathogenesis, in which oxidative stress and inflammation are the well-known molecular mechanisms. However, the underlying mechanisms of how RPE responds when exposed to drusen are still poorly understood. Programmed cell death (PCD) plays an important role in cellular responses to stress and the regulation of homeostasis and diseases. Apart from the classical apoptosis, recent studies also discovered novel PCD pathways such as pyroptosis, necroptosis, and ferroptosis, which may contribute to RPE cell death in AMD. This evidence may yield new treatment targets for AMD. In this review, we summarized and analyzed recent advances on the association between novel PCD and AMD, proposing PCD's role as a therapeutic new target for future AMD treatment.
Keyphrases
- age related macular degeneration
- oxidative stress
- cell death
- end stage renal disease
- cell cycle arrest
- chronic kidney disease
- dna damage
- multiple sclerosis
- single cell
- endoplasmic reticulum stress
- prognostic factors
- peritoneal dialysis
- diabetic rats
- signaling pathway
- current status
- stem cells
- nlrp inflammasome
- heat stress