Alzheimer
Pathway ID: SIGNOR-ADView in NDEx
Description: Alzheimer's disease (AD) is one of the major causes of dementia, AD is a brain disorder affecting the elderly and is characterized by the formation of two main protein aggregates: senile plaques and neurofibrillary tangles, which are involved in the process leading to progressive neuronal degeneration and death. The senile plaques are generated by a deposition in the human brain of fibrils of the beta-amyloid peptide (Abeta), a fragment derived from the proteolytic processing of the amyloid precursor protein (APP). Tau protein is the major component of paired helical filaments (PHFs), which form a compact filamentous network described as neurofibrillary tangles (NFTs).Two main protein kinases have been shown to be involved in anomalous tau phosphorylations: the cyclin-dependent kinase Cdk5 and glycogen synthase kinase GSK3beta. Several different studies have provided evidence implicating oxidative stress, calcium balance and mitochondrial apoptotic pathways a as major pathogenic mechanism in AD.
Curated by: Livia Perfetto
Description: Alzheimer's disease (AD) is one of the major causes of dementia, AD is a brain disorder affecting the elderly and is characterized by the formation of two main protein aggregates: senile plaques and neurofibrillary tangles, which are involved in the process leading to progressive neuronal degeneration and death. The senile plaques are generated by a deposition in the human brain of fibrils of the beta-amyloid peptide (Abeta), a fragment derived from the proteolytic processing of the amyloid precursor protein (APP). Tau protein is the major component of paired helical filaments (PHFs), which form a compact filamentous network described as neurofibrillary tangles (NFTs).Two main protein kinases have been shown to be involved in anomalous tau phosphorylations: the cyclin-dependent kinase Cdk5 and glycogen synthase kinase GSK3beta. Several different studies have provided evidence implicating oxidative stress, calcium balance and mitochondrial apoptotic pathways a as major pathogenic mechanism in AD.
Curated by: Livia Perfetto
28 Seed Entities
Organism: | Name | Primary ID |
---|---|
BCL2 | P10415 |
CDK5R1 | Q15078 |
BAX | Q07812 |
Apoptosome | SIGNOR-C230 |
TNF | P01375 |
NAE1 | Q13564 |
MAPT | P10636 |
TNFRSF1A | P19438 |
CAST | P20810 |
CASP8 | Q14790 |
CASP3 | P42574 |
PSEN2 | P49810 |
GSK3A | P49840 |
CAPN1 | P07384 |
CYCS | P99999 |
CDK5/CDK5R1 | SIGNOR-C144 |
APP | P05067 |
gamma-secretase | SIGNOR-C98 |
Apoptosis | SIGNOR-PH2 |
PSEN1 | P49768 |
Neurofibrillary tangle formation | SIGNOR-PH58 |
NCSTN | Q92542 |
APAF1 | O14727 |
FADD | Q13158 |
TRADD | Q15628 |
BID | P55957 |
Amyloid_fibril_formation | SIGNOR-PH59 |
GSK3B | P49841 |