Research Radartracking 1,762 published studies · 471 human · 11 safety signals · 58 clinical trials · 44 cancer pages · updated Sep 2026Open the Research Map →
Curcumin / Theracurmin
Turmeric polyphenol inhibiting NF-κB/STAT3, inducing apoptosis, curbing angio/metastasis; strong clinical signals as chemo adjunct with bioavailability focus.
Studies disagree on the reported direction (conflict flagged).
No human studies yet
Findings conflict across studies
No numeric effect sizes reported
Computed deterministically from the studies’ types and reported outcomes — not written by AI, and not a claim that anything works.
🏥⭐⭐⭐⭐ Strong — Supported by multiple RCTs and meta-analyses, especially for colorectal and pancreatic cancers.Turmeric extractDiferuloylmethaneTheracurmin (bioavailable form)
Forms: Curcumin capsules (500–2000 mg, with piperine or Theracurmin)
Educational only, not medical advice. OncoForge makes no claim that Curcumin / Theracurmin 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.
Simple Summary
Well-studied turmeric extract that shuts down NF-κB/STAT3 inflammation, nudges tumor cells into apoptosis, and reduces VEGF/MMPs. Bioavailability is the bottleneck—formulations like Theracurmin improve exposure. Human trials show signals across several cancers and for chemo-sensitization.
Curcumin, a turmeric-derived polyphenol, inhibits NF-κB and STAT3 pathways, reducing inflammation-driven tumor growth and metastasis. It downregulates anti-apoptotic proteins (Bcl-2, Bcl-xL), upregulates pro-apoptotic Bax, and activates caspases, inducing apoptosis. Curcumin resensitizes tumor cells to platinum-based chemotherapy by inhibiting ABC transporters and DNA repair pathways. It also suppresses VEGF, MMP-2, and MMP-9, inhibiting angiogenesis, and modulates PI3K/Akt/mTOR to limit cell proliferation.
Targets & pathways
Curated mechanistic targets reported for this agent — how it may act on cells, not proof of a clinical effect.
NF-κB ↓: Avoid stacking with other strong NF-κB inhibitors without rationale.
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 Upset MildHepatotoxicity Risk MildPregnancy Avoid
Potential interactions
CYP3A4/P-gp substrates (e.g., TKIs, chemo)MonitorModerateTheoreticalMay alter levels; pharmacist review.
What has been studied, and how strong it is, by topic. A dashed cell means no studies were found for that combination — a gap, not evidence of no effect. Open a row to see its studies.
The authors designed a new hybrid molecule called CURSAHA by fusing pharmacophores of vorinostat and curcumin. CURSAHA inhibits histone deacetylases, produces reactive oxygen species when exposed to ultrasound, and downregulates HDACs via ROS-mediated redox reactions. The compound showed antitumor activity in cell-based (in vitro) and animal (in vivo) models of breast cancer.
Studied with: ultrasound.
Key findings
CURSAHA was designed through pharmacophore fusion of Vorinostat and curcumin.
CURSAHA demonstrates broad-spectrum inhibitory activity against HDACs.
CURSAHA effectively suppresses tumor cells with overexpressed HDACs.
CURSAHA generates reactive oxygen species (ROS) under ultrasonic conditions, exhibiting sonodynamic therapeutic activity.
CURSAHA downregulates HDACs through redox reactions involving ROS.
CURSAHA exhibited robust antitumor activity in both in vitro and in vivo models.
Limitations: Study is preclinical (in vitro and in vivo models) with no human data reported in the abstract.; Abstract provides no details on animal species, sample sizes, dosing, controls, or statistical significance.; Safety, toxicity, and pharmacokinetics are not reported in the abstract.; CURSAHA is a novel compound; findings require replication and further development before clinical relevance can be assessed..
AI summary of the abstract, human-reviewed · Sep 2026. Describes what this study reported, not medical advice. View on PubMed
Biomolecules · Nov 2022 · literature review (PubMed search, accessed 18 June 2022)
Curcuminnon-small cell lung cancer (NSCLC)lung carcinomalung neoplasms
This paper is a literature review that collected reports on curcumin and its analogs in non-small cell lung cancer (PubMed search accessed 18 June 2022). The authors summarize reported anti-NSCLC mechanisms, review combinations of curcumin with chemotherapeutic agents, and used Discovery Studio to speculate on interactions with molecular targets. They note that many studies report anticancer effects of curcumin/analogs but that results of clinical trials have been inconsistent. The review concludes that curcumin and its analogs may be promising therapeutic agents or adjuvants for lung carcinoma despite existing challenges.
Studied with: chemotherapeutic agents.
Key findings
Advances in NSCLC therapy (chemoradiotherapy, targeted therapy, immunotherapy) have improved survival but overall recovery and survival rates remain low.
There is an urgent need for novel NSCLC drugs or combination therapies with less toxicity.
Anticancer effectiveness of curcumin and some curcumin analogs has been reported in many studies.
Results from clinical trials of curcumin in NSCLC have been inconsistent.
The authors collected recent reports on anti-NSCLC mechanisms of curcumin/analogs and their combinations with chemotherapeutic agents via PubMed.
The authors used Discovery Studio to speculate on interplay between curcumin and various molecular targets relevant to NSCLC.
Despite challenges, curcumin/curcumin analogs may serve as promising therapeutic agents or adjuvants for lung carcinoma treatment.
Limitations: This article is a literature review rather than original experimental work.; The abstract states that clinical trial results are inconsistent, limiting clinical conclusions.; The interaction analysis using Discovery Studio is speculative/in silico and not experimentally validated in this paper.; Search was limited to PubMed reports accessed up to 18 June 2022 (date-limited review)..
AI summary of the abstract, human-reviewed · Jun 2026. Describes what this study reported, not medical advice. View on PubMed · Full text
This is a review article summarizing research on curcumin (the yellow Indian spice) and its effects in endometrial carcinoma. The review describes investigations of curcumin's potential anti-cancer activity and its roles in pathways involved in carcinogenesis. The abstract does not present original experimental data or quantitative results.
Key findings
Curcumin has been adopted for investigation by the scientific community as a potential anti-cancer agent for endometrial carcinoma.
The review focuses on the effect of curcumin on endometrial cancer and its role in specific pathways involved in carcinogenesis.
No original data or quantitative outcomes are reported in the abstract.
Limitations: Review article; no original experimental data reported in the abstract.; Abstract does not specify which molecular pathways or mechanisms are involved.; No details on methods, study selection, or quantitative results are provided in the abstract..
AI summary of the abstract, human-reviewed · Sep 2026. Describes what this study reported, not medical advice. View on PubMed · Full text
What changed recently
The latest additions to Curcumin / Theracurmin's evidence base, and anything that's been retracted.
Cancers where Curcumin / Theracurmin reported positive results
Where at least one study reported a positive result, shown with the full picture, not just the wins. Positive results are more likely to be published, and most of these are early lab or animal studies that may not translate to people. This reports what studies found, not what works.
Limitations: Study is preclinical (in vitro and in vivo models) with no human data reported in the abstract.; Abstract provides no details on animal species, sample sizes, dosing, controls, or statistical significance.; Safety, toxicity, and pharmacokinetics are not reported in the abstract.; CURSAHA is a novel compound; findings require replication and further development before clinical relevance can be assessed..
Limitations: Review article; no original experimental data reported in the abstract.; Abstract does not specify which molecular pathways or mechanisms are involved.; No details on methods, study selection, or quantitative results are provided in the abstract..
Evidence at a glance: Curcumin / Theracurmin by cancer
A deterministic grade of what published studies report for each: strength of evidence, the reported direction, and the largest credible effect, strongest-evidence first. This summarizes findings; it is not a claim that anything works.
No human studies yet · No numeric effect sizes reported · Based on a single study.
Dose: as studied, not a recommendation
These are doses as studied or reported, never a recommendation. The right amount of Curcumin / Theracurmin 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: 500–8000 mg (po) Divided into 2–3 doses daily. Oncology adjunct: 1000–4000 mg/day (enhanced forms like Theracurmin for better absorption); up to 8000 mg/day in trials., No Rx required. Use bioavailable forms (e.g., with piperine/Theracurmin); take with meals. Clinician oversight for oncology; monitor LFTs at high doses..
Clinical trials studying Curcumin / Theracurmin
0 ongoing · 0 completed · tracked from ClinicalTrials.gov. Recruiting is not the same as proven, and completed is not the same as positive — read the results. Not a recommendation.
Curcumin / Theracurmin 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.