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Necroptosis Signaling Pathways in Stroke: From Mechanisms to Therapies
- Source :
- Current Neuropharmacology
- Publication Year :
- 2018
- Publisher :
- Bentham Science Publishers, 2018.
-
Abstract
- It has been confirmed that apoptosis, autophagy and necrosis are the three major modes of cell death. For a long time, necrosis is regarded as a deranged or accidental cell demise. In recent years, there is evidence showing that necrotic cell death can be a well regulated and orchestrated event, which is also known as programmed cell death or "necroptosis". Necroptosis can be triggered by a variety of external stimuli and regulated by a caspase-independent pathway. It plays a key role in the pathogenesis of some diseases including neurological diseases. In the past two decades, a variety of studies have revealed that the necroptosis related pathway is activated in stroke, and plays a crucial role in the pathogenesis of stroke. Moreover, necroptosis may serve as a potential target in the therapy of stroke because genetic or pharmacological inhibition of necroptosis has been shown to be neuroprotective in stroke in vitro and in vivo. In this review, we briefly summarize recent advances in necroptosis, introduce the mechanism and strategies targeting necroptosis in stroke, and finally propose some issues in the treatment of stroke by targeting necroptosis.
- Subjects :
- 0301 basic medicine
Programmed cell death
Necroptosis
Cell
necroptosis
Neuroprotection
Article
Nec-1
03 medical and health sciences
Necrosis
Medicine
Animals
Humans
Pharmacology (medical)
RIP1
RIP3
Stroke
Pharmacology
business.industry
Mechanism (biology)
Autophagy
General Medicine
medicine.disease
Psychiatry and Mental health
030104 developmental biology
medicine.anatomical_structure
Neurology
Apoptosis
Neurology (clinical)
business
Neuroscience
MLKL
Signal Transduction
Subjects
Details
- Language :
- English
- ISSN :
- 18756190 and 1570159X
- Volume :
- 16
- Issue :
- 9
- Database :
- OpenAIRE
- Journal :
- Current Neuropharmacology
- Accession number :
- edsair.doi.dedup.....8058587f13a40ac2a9c13bf687839ff3