| Rank |
Pathway / Axis |
Cancer Cells (↑ / ↓ / ↔) |
Normal Cells (↑ / ↓ / ↔) |
TSF |
Primary Effect |
Notes / Interpretation |
| 1 |
PI3K/Akt/mTOR |
↓ proliferation; ↓ survival signaling |
↔ / mild ↓ (cytoprotective context) |
R→G |
Growth suppression |
Core mechanistic axis across multiple tumor models (breast, lung, colon, prostate). |
| 2 |
MAPK (ERK, JNK, p38) |
↑ JNK/p38 (pro-apoptotic); ↓ ERK (proliferative) |
↔ (dose-dependent) |
R |
Apoptosis induction |
Often stress-activated signaling; balance of ERK vs JNK determines outcome. |
| 3 |
NF-κB |
↓ transcription of inflammatory & anti-apoptotic genes |
↓ inflammatory tone |
R→G |
Anti-inflammatory / anti-survival |
Reduces cytokine signaling and tumor microenvironment support pathways. |
| 4 |
ROS |
↑ (high concentration; pro-oxidant apoptosis) |
↔ / ↓ (antioxidant at low conc.) |
P→R |
Mitochondrial stress |
Biphasic: antioxidant at dietary levels; pro-oxidant at higher in-vitro doses. |
| 5 |
NRF2 |
↔ / ↓ (context-dependent) |
↑ cytoprotective response |
G |
Redox adaptation |
May activate antioxidant genes in normal cells; persistent activation in tumors could support resistance. |
| 6 |
Intrinsic apoptosis (Bax/Bcl-2, caspases) |
↑ Bax; ↓ Bcl-2; ↑ caspase-3/9 |
↔ |
R→G |
Mitochondrial apoptosis |
Common downstream convergence of ROS + PI3K suppression. |
| 7 |
Ca2+ signaling |
↑ mitochondrial Ca2+ (subset models) |
↔ |
R |
Apoptotic amplification |
Not universal; observed in certain carcinoma lines. |
| 8 |
HIF-1α / Angiogenesis |
↓ HIF-1α; ↓ VEGF (model-dependent) |
↔ |
G |
Anti-angiogenic potential |
Observed in hypoxia models; translational impact uncertain. |
| 9 |
Ferroptosis |
↔ (indirect; limited data) |
↔ |
R |
Redox-linked sensitivity (theoretical) |
No consistent ferroptosis signature established. |
| 10 |
Clinical Translation Constraint |
Low oral bioavailability; rapid conjugation; in-vitro concentrations commonly exceed systemic exposure; limited human interventional oncology data. |
— |
PK / Evidence |
Dietary intake likely below cytotoxic range; delivery systems (nano-formulations) under investigation. |