Kaempferol
Flavonoid: Anti-angiogenic (VEGF/HIF-1α ↓), pro-apoptotic, PI3K/Akt inhibitor; preclinical adjunct for solid tumors.
Forms: Dietary (e.g., in kale, tea, berries) · Standardized supplement (50-100 mg capsules)
Key Takeaway
Dietary flavonoid that lowers HIF-1α/VEGF signaling (anti-angiogenic), nudges PI3K/Akt and ERK down, and triggers caspase-mediated apoptosis with G2/M arrest in multiple tumor models. Promising as an adjunct; human oncology trials remain limited.
Evidence at a glance
Strong mechanistic preclinical support across models; synergies noted with chemo; human PK/safety established but oncology efficacy unproven.
How it may work
Kaempferol suppresses VEGF and HIF-1α under hypoxia, inhibiting angiogenesis; modulates Bcl-2/Bax with caspase-3/9 activation to induce apoptosis; arrests cells at G2/M via JNK/p38; and inhibits PI3K/Akt and ERK signaling to reduce proliferation and migration. Preclinical efficacy spans colon, breast, lung, and ovarian cancers.
Targets & pathways
Curated mechanistic targets reported for this agent — how it may act on cells, not proof of a clinical effect.
Often studied / combined with
Combinations reported in the literature, not a protocol or a recommendation.
- Cisplatin: Amplified caspase activation and G2/M arrest in ovarian cancer.
- Quercetin: Complementary flavonoid effects on apoptosis/cytostasis in breast/colon.
- Curcumin: Enhanced VEGF inhibition and anti-proliferative synergy in colorectal models.
- Resveratrol: Cooperative apoptosis induction via shared pathways in breast cancer.
Overlapping mechanisms
- PI3K/Akt: Redundant with other natural PI3K modulators (e.g., EGCG); prioritize based on bioavailability.
- Apoptosis: Multiple pro-apoptotic naturals may saturate caspases without added benefit.
Safety & interactions
Severity and how well-established each signal is are shown separately. Verify everything with your oncologist or pharmacist — absence here does not mean safe.
Timing
- With-meal: Improves absorption of fat-soluble flavonoid.
- AM/PM: Divided doses for steady exposure.
References
- DOI 10.1186/s13765-025-00992-0: Kaempferol anti-cancer review
- PMC2770884: Kaempferol inhibits VEGF/HIF-1α in colon cancer
- PMC10854650: Apoptosis induction via JNK/p38 in breast cancer
- DOI 10.1016/j.bbrc.2010.06.094: PI3K/Akt inhibition in ovarian cancer
- DOI 10.3390/nu12061619: Synergy with cisplatin in ovarian models
- PMC10221542: Combination with quercetin in colon cancer
Research
No published studies for Kaempferol yet
New studies appear here once they’ve been reviewed. Browse all studies.
Dose: as studied, not a recommendation
Ranges seen in adjunct / practice use: 10–100 mg/day (po) divided with meals; dietary sources preferred, Preclinical doses 20-100 µM in vitro; human anti-cancer dosing extrapolated ~50 mg/day; bioavailability low—consider liposomal forms..
Trials studying Kaempferol
No actively-recruiting trials matched right now. Recruiting is not the same as proven. Search ClinicalTrials.gov →