STUDY: Vitamin C + Grape Seed Extract Outperforms Chemotherapy for Tumor Reduction in Mice
Natural combo cut cancerous tumor volume by 76.61%, surpassing the “red devil” doxorubicin (68.82%) in a head-to-head preclinical study.
This article originally appeared on Focal Points and was republished with permission.
Guest post by Nicolas Hulscher, MPH
A recent preclinical cancer study produced a striking result: in a mouse solid tumor model (Ehrlich carcinoma), a combination of Grape Seed Extract (GSE) + Vitamin C reduced tumor volume more than chemotherapy.
Researchers compared multiple treatment arms—including doxorubicin (DOX, nicknamed the “red devil”) as the chemo comparator—and found that the GSE + Vitamin C group showed the greatest mean tumor volume reduction, outperforming DOX in this experiment.
Greater tumor reduction than chemotherapy
Untreated tumor controls (SEC): 0% reduction (mean tumor volume: 735.40 mm³ ± 11.89)
Vitamin C alone (AA): 56.94% reduction (316.69 mm³ ± 8.74)
Grape Seed Extract alone (GSE): 63.40% reduction (269.14 mm³ ± 13.69)
Chemotherapy (doxorubicin): 68.82% reduction (229.27 mm³ ± 6.898)
GSE + Vitamin C (GSE + AA): 76.61% reduction (171.977 mm³ ± 4.151)
In other words, within this model, the GSE + Vitamin C combination produced the greatest mean tumor shrinkage, exceeding the reduction seen with doxorubicin chemotherapy.
GSE + Vitamin C rewired tumor biology and flipped the immune microenvironment
Beyond simply reducing tumor size, the GSE + Vitamin C combination produced marker changes consistent with a real mechanistic anti-cancer effect—suppressing tumor growth signals while activating tumor cell death and immune pressure:
↓ Ki-67 (reduced tumor proliferation)
↑ caspase-3 (increased apoptosis / programmed tumor cell death)
↓ FOXP3+ Tregs (immunosuppressive regulatory cells tumors exploit to evade immune clearance)
↑ CD8+ cytotoxic T-cells and ↑ CD4+ T-cells infiltrating tumor tissue
Taken together, these findings suggest the combo wasn’t just slowing growth—it was pushing tumors toward cell death while making the tumor environment less immune-protected and more vulnerable to immune attack.
Conclusion
This is a compelling head-to-head preclinical comparison—but it remains a mouse study. Still, the effect size, the chemo comparator, and the immune remodeling signals make it a result worth serious attention and follow-up.
In this mouse tumor model, GSE + Vitamin C outperformed the “red devil” chemotherapy, achieving 76.61% vs. 68.82% mean tumor volume reduction, while also showing tumor marker and immune-environment changes consistent with true anti-cancer activity. And this isn’t surprising—a large body of research has documented anti-cancer mechanisms of vitamin C across multiple tumor systems, especially through oxidative stress–mediated tumor injury and immune support.
These findings strengthen the case that low-cost, biologically coherent combinations deserve serious clinical investigation.
Epidemiologist and Foundation Administrator, McCullough Foundation
www.mcculloughfnd.org
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