Acer okamotoanum / PSEN2/PS-2 Cancer Research Results

AO, Acer okamotoanum: Click to Expand ⟱
Features:

Acer okamotoanum - Acer okamotoanum Extract

Alternative Names: Acer okamotoanum, Ulleungdo maple

Type: Botanical extract / flavonoid-rich plant product

Source: Acer okamotoanum is a maple species native to Korea, particularly Ulleung Island. Experimental studies have used leaf extracts and solvent fractions, including flavonoid-rich ethyl acetate fractions.

Active Constituents: Reported constituents include isoquercitrin, quercitrin, afzelin, and other phenolic and flavonoid compounds.

Function: Acer okamotoanum extracts exhibit antioxidant, anti-inflammatory, cytoprotective, and neuroprotective activities. Experimental studies show reductions in reactive oxygen species, lipid peroxidation, inflammatory signaling, and apoptotic damage, together with preservation of neuronal viability and cellular stress resistance.

Alzheimer's Disease: Preclinical evidence suggests potential neuroprotective and cognition-preserving effects. Acer okamotoanum extract has improved learning and memory and reduced oxidative stress in experimental models involving amyloid-β and metabolic stress. Constituents including isoquercitrin, quercitrin, and afzelin may contribute to these effects through antioxidant, anti-inflammatory, and amyloid-related mechanisms. Clinical efficacy for Alzheimer's disease has not been established.



PSEN2/PS-2, Presenilin 2: Click to Expand ⟱
Source:
Type:

PSEN2 - Presenilin 2

Type: Intramembrane aspartyl protease / catalytic γ-secretase complex subunit

Function: PSEN2 is a catalytic component of the γ-secretase complex, together with nicastrin, APH1, and PEN2. The complex performs intramembrane proteolysis of multiple substrates including amyloid precursor protein (APP) and Notch receptors. γ-Secretase cleavage of APP generates amyloid-β peptides including Aβ40 and Aβ42. PSEN2 also participates in endolysosomal, calcium, mitochondrial, and cellular signaling functions.

Alzheimer's Disease: ↕ Altered function. Pathogenic PSEN2 mutations cause rare autosomal-dominant familial Alzheimer's disease by altering γ-secretase processing of APP. Many disease-associated mutations increase the relative production of aggregation-prone Aβ42, producing an increased Aβ42/Aβ40 ratio. The primary Alzheimer's mechanism therefore reflects altered PSEN2/γ-secretase activity rather than a consistent increase or decrease in PSEN2 expression.



Scientific Papers found: Click to Expand⟱
7839- AO,  ISQ,    The Protective Effects of Acer okamotoanum and Isoquercitrin on Obesity and Amyloidosis in a Mouse Model
- in-vivo, AD, NA - in-vivo, Obesity, NA
*Dose↝, *Obesity↓, *Leptin↓, *adiP↑, *hepatoP↑, *PSEN1/PS1↓, *PSEN2/PS-2↓, *BACE/β-secretase↓, *eff↑,

Showing Research Papers: 1 to 1 of 1

* indicates research on normal cells as opposed to diseased cells
Total Research Paper Matches: 1

Pathway results for Effect on Cancer / Diseased Cells:


Total Targets: 0

Pathway results for Effect on Normal Cells:


NA, unassigned(tgid=0)

PSEN1/PS1↓, 1,   PSEN2/PS-2↓, 1,  

Core Metabolism/Glycolysis(tgid=4)

adiP↑, 1,  

Protein Aggregation(tgid=19)

BACE/β-secretase↓, 1,  

Hormonal & Nuclear Receptors(tgid=20)

Leptin↓, 1,  

Drug Metabolism & Resistance(tgid=21)

Dose↝, 1,   eff↑, 1,  

Functional Outcomes(tgid=23)

hepatoP↑, 1,   Obesity↓, 1,  
Total Targets: 9

Scientific Paper Hit Count for: PSEN2/PS-2, Presenilin 2
Query results interpretion may depend on "conditions" listed in the research papers.
Such Conditions may include : 
  -low or high Dose
  -format for product, such as nano of lipid formations
  -different cell line effects
  -synergies with other products 
  -if effect was for normal or cancerous cells
Filter Conditions: Pro/AntiFlg:%  IllCat:%  CanType:%  Cells:%  prod#:466  Target#:1699  State#:%  Dir#:1
wNotes=0 sortOrder:rid,rpid

 

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