Research Radartracking 2 published studies · 1 clinical trials · 2 cancer pages · updated Jun 2026Open the Research Map →

Resveratrol

Stilbenoid: SIRT1 ↑, NF-κB/apoptosis mod; moderate adjunct in breast/prostate/colorectal/lung.

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Human-reviewed · How we review →

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👥⭐⭐⭐ Moderate — Early human studies plus extensive preclinical data; definitive oncology RCTs remain limited.RSVTrans-resveratrol3,5,4'-Trihydroxy-trans-stilbene

Forms: Micronized capsules (250-500 mg trans-resveratrol) · Liposomal or cyclodextrin-complexed for bioavailability

Educational only, not medical advice. OncoForge makes no claim that Resveratrol treats, prevents, or cures any condition, beyond what the linked studies show. Evidence levels vary; effects may not translate to people, and some compounds can cause harm. Always coordinate with your oncology team.

Key Takeaway

Pleiotropic polyphenol that activates SIRT1, suppresses NF-κB–driven inflammation, and promotes apoptosis; adjunct potential with mixed but encouraging human signals.

Evidence at a glance

Tier 2 · animalBreastProstateColorectalLung

Preclinical SIRT/NF-κB dominance; phase II PSA signals in prostate; meta-QoL modest; ongoing combos in CRC/breast; bioavailability hurdle noted.

How it may work

Resveratrol (RSV) activates SIRT1→FOXO/PGC-1α deacetylation, enhancing DNA repair/mitochondrial efficiency and reducing senescence signaling. It inhibits NF-κB (IKK/p65), lowering COX-2/IL-6/TNF and angiogenic VEGF. RSV primes intrinsic apoptosis (Bax↑/Bcl-2↓, caspase-3/9) and can modulate ER/AR signaling in hormone-responsive tumors. Synergistic effects with chemo/radiation are reported preclinically and in small trials.

Targets & pathways

Curated mechanistic targets reported for this agent — how it may act on cells, not proof of a clinical effect.

  • SirtuinSIRT1 activation for DNA repair/mitochondria
  • NF-κBIKK/p65 inhibition, cytokine reduction
  • ApoptosisBax/Bcl-2 modulation, caspase activation
  • VEGFAnti-angiogenic effects
  • ER/ARModHormone signaling modulation
SirtuinNF-κBApoptosis

Often studied / combined with

Combinations reported in the literature, not a protocol or a recommendation.

Overlapping mechanisms

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.

Risk categories
Gi UpsetEstrogenicDrug Interactions
Potential interactions
  • anticoagulantsMonitorModerateTheoreticalPotential platelet inhibition.
  • CYP3A4 substratesMonitorLowTheoreticalInduction may lower levels (e.g., statins).
  • DoxorubicinSynergizeLowTheoreticalApoptosis enhancement in breast.

Timing

References

Research

No published studies for Resveratrol yet

New studies appear here once they’ve been reviewed. Browse all studies.

Dose: as studied, not a recommendation

These are doses as studied or reported, never a recommendation. The right amount of Resveratrol depends on you, your other medicines, and your situation; decide it with your oncology team and pharmacist, not from a web page.

Ranges seen in adjunct / practice use: 250–1000 mg/day (po) divided BID; micronized for absorption, Adjunct 500 mg/day; up to 1 g for preclinical extrapolation; trans-isomer preferred; cycle if GI issues..

Trials studying Resveratrol

No actively-recruiting trials matched right now. Recruiting is not the same as proven. Search ClinicalTrials.gov →

Appears in these protocol claims

Resveratrol is named in these protocols discussed online. Listed for transparency: being part of a protocol is not evidence that it works, and OncoForge does not endorse them.

Inclusion here is not an endorsement. OncoForge makes no claim beyond what the linked studies show. Discuss anything on this page with your oncology team before acting on it.

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