DMF (Dimethyl Fumarate) †Rx
DMF activates NRF2 (antioxidant induction) but overloads tumor ROS; inhibits NF-κB/PI3K for apoptosis. Preclinical strong in GBM/breast/CRC; no oncology trials yet—monitor lymphopenia/flushing.
Forms: Oral delayed-release capsules (Rx, 120–240 mg)
Simple Summary
MS drug that turns on the NRF2 defense program while paradoxically pushing over-stressed cancer cells into ROS-driven death. Strong lab support; clinical cancer trials are not yet established.
Evidence at a glance
Preclinical mechanistic/animal robust; human oncology absent (MS data translates safety).
How it may work
DMF alkylates Keap1 to activate NRF2, inducing antioxidant/phase-II enzymes (HO-1, NQO1). Tumor cells, already redox-stressed, can tip into lethal ROS with DMF. DMF also inhibits NF-κB and downshifts PI3K/AKT, promoting apoptosis in multiple preclinical models.
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.
- Temozolomide: Apoptosis enhancement in GBM.
- Radiotherapy: Tumor sensitivity boost in breast.
- Curcumin: ROS/apoptosis in GBM.
- Resveratrol: NRF2/ROS in CRC.
- EGCG: NF-κB/apoptosis in breast.
- Quercetin: ROS/PI3K in GBM.
Overlapping mechanisms
- NRF2 ↑ / ROS ↑: Caution stacking with other NRF2 activators; may desensitize tumors or amplify normal cell protection.
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.
- Aspirin/NSAIDsConsiderBeneficialTheoreticalPre-dose aspirin mitigates flushing.
- Redox agents (e.g., high-dose antioxidants)MonitorModerateTheoreticalMay blunt selective ROS effect in tumors.
- Temozolomide / RadiotherapyConsiderBeneficialTheoreticalSynergistic apoptosis/ROS in GBM/breast.
- Curcumin / Resveratrol / EGCG / QuercetinConsiderBeneficialTheoreticalEnhances ROS/apoptosis/NF-κB/PI3K inhibition.
Timing
- With food: Reduces GI upset.
- BID dosing: Steady-state levels; titrate up over weeks.
- 30 min after aspirin (optional): For flushing prophylaxis.
References
Research
No published studies for DMF (Dimethyl Fumarate) †Rx 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: 120–480 mg (po) Standard MS regimen: 120 mg BID for 1 week, then 240 mg BID (total 480 mg/day). Investigational cancer use: similar starting doses (e.g., 240–360 mg/day) with escalation; no established oncology HED from animals as primarily human-derived data., Rx required. Aspirin 325 mg 30 min prior may reduce flushing. Titrate slowly to minimize GI/flushing. Pulsed or lower-dose schedules explored preclinically for cancer. Strict clinician oversight; monitor CBC/LFTs monthly..
Trials studying DMF (Dimethyl Fumarate) †Rx
No actively-recruiting trials matched right now. Recruiting is not the same as proven. Search ClinicalTrials.gov →