Scientists from USC and the IFOM Cancer Institute in Milan have found that a fasting-mimicking diet could be more effective at treating some types of cancer when combined with vitamin C.
In multiple studies on mice, researchers found that the combination delayed tumor progression in multiple mouse models of colorectal cancer; in some mice, it caused disease regression. The results were published in the journal Nature Communications.
“For the first time, we have demonstrated how a completely nontoxic intervention can effectively treat an aggressive cancer,” said Valter Longo, the study’s senior author and the director of the USC Longevity Institute at the USC Leonard Davis School of Gerontology and a professor of biological sciences at the USC Dornsife College of Letters, Arts and Sciences. “We have taken two treatments that are studied extensively as interventions to delay aging — a fasting-mimicking diet and vitamin C — and combined them as a powerful treatment for cancer.”
The researchers said that, while fasting remains a challenging option for cancer patients, a safer, more feasible option is a low-calorie, plant-based diet that causes cells to respond as if the body were fasting. Their findings suggest that a low-toxicity treatment of fasting-mimicking diet plus vitamin C has the potential to replace more toxic treatments.
For the first time, we have demonstrated how a completely nontoxic intervention can effectively treat an aggressive cancer.
Results of prior research on the cancer-fighting potential of vitamin C have been mixed. Recent studies, though, are beginning to show some efficacy, especially in combination with chemotherapy. In this new study, the research team wanted to find out whether a fasting-mimicking diet could enhance the high-dose vitamin C tumor-fighting action by creating an environment that would be unsustainable for cancer cells but still safe for normal cells.
“Our first in vitro experiment showed remarkable effects,” Longo said. “When used alone, fasting-mimicking diet or vitamin C alone reduced cancer cell growth and caused a minor increase in cancer cell death. But when used together, they had a dramatic effect, killing almost all cancerous cells.”
Longo and his colleagues detected this strong effect only in cancer cells that had a mutation regarded as one of the most challenging targets in cancer research. These mutations in the KRAS gene signal that the body is resisting most cancer-fighting treatments, and they reduce a patient’s survival rate. KRAS mutations occur in approximately a quarter of all human cancers and are estimated to occur in up to half of all colorectal cancers.
Why fasting and vitamin C work well in tandem
The study also provided clues about why previous studies of vitamin C as a potential anticancer therapy showed limited efficacy. By itself, a vitamin C treatment appears to trigger the KRAS-mutated cells to protect cancer cells by increasing levels of ferritin, a protein that binds iron. But by reducing levels of ferritin, the scientists managed to increase vitamin C’s toxicity for the cancer cells. Amid this finding, the scientists also discovered that colorectal cancer patients with high levels of the iron-binding protein have a lower chance of survival.
“In this study, we observed how fasting-mimicking diet cycles are able to increase the effect of pharmacological doses of vitamin C against KRAS-mutated cancers,” said Maira Di Tano, a study co-author at the IFOM, FIRC Institute of Molecular Oncology in Milan. “This occurs through the regulation of the levels of iron and of the molecular mechanisms involved in oxidative stress. The results particularly pointed to a gene that regulates iron levels: heme-oxygenase-1.”
The research team’s prior studies showed that fasting and a fasting-mimicking diet slow cancer’s progression and make chemotherapy more effective in tumor cells while protecting normal cells from chemotherapy-associated side effects. The combination enhances the immune system’s anti-tumor response in breast cancer and melanoma mouse models.
The scientists believe cancer will eventually be treated with low-toxicity drugs in a manner similar to how antibiotics are used to treat infections that kill particular bacteria but can be replaced by other drugs if they prove ineffective.
To move toward that goal, they needed to first test two hypotheses: that their nontoxic combination interventions would work in mice, and that results would look promising for human clinical trials. In this new study, they said they’ve demonstrated both.
At least five clinical trials — including one at USC on breast cancer and prostate patients — are now investigating the effects of fasting-mimicking diets in combination with different cancer-fighting drugs.
Additional authors include Franca Raucci and Claudio Vernieri of IFOM, FIRC Institute of Molecular Oncology, Milan; Irene Caffa and Alessio Nencioni of the Department of Internal Medicine, University of Genoa and IRCCS Ospedale Policlinico San Martino, Genoa, Italy; Roberta Buono, Maura Fanti and Sebastian Brandhorst of the Longevity Institute, USC Leonard Davis School of Gerontology and Department of Biological Sciences; Giuseppe Curigliano of the University of Milan, Department of Oncology and Hemato-Oncology and Division of Early Drug Development, European Institute of Oncology, IRCCS, Milan; Filippo De Braud of the University of Milan, Department of Oncology and Hemato-Oncology, and Medical Oncology Department, Fondazione IRCCS Istituto Nazionale Tumori, Milan.
The study was funded by Associazione Italiana Ricerca sul Cancro grant number 21820 and by NIA/NIH Grant # PO1 AG055369.
Longo is the founder of and has an ownership interest in L-Nutra; the company’s food products are used in studies of the fasting-mimicking diet. Longo’s interest in L-Nutra was disclosed and managed per USC’s conflicts-of-interest policies. USC has an ownership interest in L-Nutra and the potential to receive royalty payments from L-Nutra. USC’s financial interest in the company has been disclosed and managed under USC’s institutional conflict of interest policies.