Sesame seeds and Oil / NO Cancer Research Results

Sesame, Sesame seeds and Oil: Click to Expand ⟱
Features:
Sesame (particularly sesame seeds and sesame oil) has been studied for its potential neuroprotective effects, including relevance to Alzheimer’s disease (AD)

Sesame (seeds/oil) — AD relevance: Preclinical literature (sesamin/sesamolin/sesamol and sesame oil) supports neuroprotection via antioxidant + anti-inflammatory mechanisms, with reported effects on amyloid toxicity/aggregation in models. Human AD-specific clinical evidence is limited.

Primary mechanisms (conceptual rank):
1) ↓ Oxidative stress (ROS ↓; lipid peroxidation ↓)
2) ↓ Neuroinflammation (NF-κB ↓; p38MAPK tone ↓; microglial activation ↓)
3) ↑ Neurotrophic/synaptic support (BDNF ↑ in some models; network resilience)
4) Aβ toxicity/aggregation ↓ (preclinical; model-dependent)

Bioavailability / PK relevance: Effects are typically chronic (weeks) and metabolite/remodeling driven.

Clinical evidence status: Predominantly preclinical for AD mechanisms; not established as disease-modifying in humans.

-Sesame seeds are rich in sesamin, sesamol, and sesaminol, lignans with strong antioxidant properties.
-Sesamol has been shown to inhibit pro-inflammatory cytokines like TNF-α, IL-1β, and IL-6, and suppress NF-κB signaling
-may inhibit acetylcholinesterase (AChE)
-Sesamol may help inhibit Aβ aggregation
Mechanism	                Effect
↓ ROS (Oxidative stress)	Protects neurons from oxidative damage
↓ NF-κB	                        Reduces neuroinflammation
↓ AChE	                        Increases acetylcholine levels
↓ Aβ aggregation	        Limits amyloid plaque formation
↑ BDNF	                        Supports neurogenesis

Nutritional Richness
-Healthy fats: High in monounsaturated and polyunsaturated fats (especially omega-6)
-Protein: A good plant-based protein source
-Minerals: Rich in calcium, magnesium, iron, zinc, selenium, and copper
-Vitamins: Contains B vitamins (especially B1, B3, B6), vitamin E

-High in calories and fats—consume in moderation

Sesame Seeds / Sesame Oil — AD / Neurodegeneration Pathway Map

RankPathway / AxisCellsTSFPrimary EffectNotes / Interpretation
1ROS / lipid peroxidation ↓P/R Reduced oxidative burden Core neuroprotective mechanism across sesamin/sesamol studies (oxidative injury models).
2Neuroinflammation (NF-κB; microglial activation) ↓R/G Lower inflammatory stress Microglial inhibition and reduced inflammatory signaling reported in neurodegeneration models.
3p38MAPK stress signaling ↓ (model-dependent)R/G Reduced stress-activated damage signaling Highlighted in sesame-oil AD rodent work as part of NF-κB/p38 coupling.
4BDNF / synaptic support ↑ (model-dependent)G Plasticity / resilience support Often presented as downstream of reduced inflammation/oxidative stress; typically requires sustained exposure.
5Aβ toxicity / aggregation ↓ (preclinical)G Reduced amyloid-associated injury Sesamin has reported anti-Aβ aggregation/toxicity effects in models; human biomarker confirmation limited.
6NRF2 axis ↔ / ↑ (context-dependent)R/G Stress-defense regulation Often inferred/secondary to antioxidant enzyme induction; not always directly measured.
7Ca²⁺ homeostasis / excitotoxic vulnerability ↔ / stabilized (indirect)P/R Excitotoxic buffering (supportive) Secondary to mitochondrial/redox support; treat as secondary unless explicit Ca²⁺ endpoints exist.
8Clinical Translation Constraint ↓ (constraint)— Preclinical-dominant evidence AD evidence is largely animal/cell-model based; dosing forms (oil vs isolated lignans) and human endpoints remain insufficient for disease-modifying claims.

TSF legend: P: 0–30 min; R: 30 min–3 hr; G: >3 hr
NO, Nitric Oxide: Click to Expand ⟱
Source:
Type:
Once the cancer has begun, NO seems to play a protumoral role rather than antitumoral one as the concentration required to cause tumor cell cytotoxicity cannot be achieved by cancer cells.
The mechanistic roles of nitric oxide (NO) during cancer progression have been important considerations since its discovery as an endogenously generated free radical. Nonetheless, the impacts of this signaling molecule can be seemingly contradictory, being both pro-and antitumorigenic, which complicates the development of cancer treatments based on the modulation of NO fluxes in tumors. At a fundamental level, low levels of NO drive oncogenic pathways, immunosuppression, metastasis, and angiogenesis, while higher levels lead to apoptosis and reduced hypoxia and also sensitize tumors to conventional therapies. However, clinical outcome depends on the type and stage of the tumor as well as the tumor microenvironment.
Nitric oxide is generated by three main nitric oxide synthase isoforms: neuronal (nNOS), endothelial (eNOS), and inducible (iNOS).

– In many cancers, especially under inflammatory conditions, iNOS expression is upregulated. In contrast, eNOS levels may also be altered in cancers such as breast or prostate cancer.

• Expression Patterns in Tumors:
– Elevated iNOS expression is commonly observed in various tumor types (e.g., colon, breast, lung, and melanoma) and is often associated with an inflammatory microenvironment.

– Changes in eNOS and nNOS expression have also been reported and may contribute to angiogenesis and tumor blood flow regulation.
Scientific Papers found: Click to Expand⟱
4190- Sesame,    Sesame Seeds: A Nutrient-Rich Superfood
- Review, NA, NA
*antiOx↑, *LDL↓, *Aβ↓, *TNF-α↓, *SOD↑, *SIRT1↑, *Catalase↑, *GSH↑, *MDA↓, *GSTs↑, *IL4↑, *GPx↑, *COX2↓, *PGE2↓, *NO↓, CDK2↑, COX2↑, MMP9↑, ICAM-1↓, *BDNF↑, *PPARγ↑, *AChE↓, *Inflam↓, *HO-1↑, *NF-kB↓, *ROS↓,

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:


Cell Cycle & Senescence ⓘ

CDK2↑, 1,  

Migration ⓘ

MMP9↑, 1,  

Immune & Inflammatory Signaling ⓘ

COX2↑, 1,   ICAM-1↓, 1,  
Total Targets: 4

Pathway results for Effect on Normal Cells:


Redox & Oxidative Stress ⓘ

antiOx↑, 1,   Catalase↑, 1,   GPx↑, 1,   GSH↑, 1,   GSTs↑, 1,   HO-1↑, 1,   MDA↓, 1,   ROS↓, 1,   SOD↑, 1,  

Core Metabolism/Glycolysis ⓘ

LDL↓, 1,   PPARγ↑, 1,   SIRT1↑, 1,  

Angiogenesis & Vasculature ⓘ

NO↓, 1,  

Immune & Inflammatory Signaling ⓘ

COX2↓, 1,   IL4↑, 1,   Inflam↓, 1,   NF-kB↓, 1,   PGE2↓, 1,   TNF-α↓, 1,  

Synaptic & Neurotransmission ⓘ

AChE↓, 1,   BDNF↑, 1,  

Protein Aggregation ⓘ

Aβ↓, 1,  
Total Targets: 22

Scientific Paper Hit Count for: NO, Nitric Oxide
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#:365  Target#:563  State#:%  Dir#:%
  wNotes=0  sortOrder:rid,rpid

 

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