Literature DB >> 30967651

Targeting cancer vulnerabilities with high-dose vitamin C.

Bryan Ngo1, Justin M Van Riper2, Lewis C Cantley3, Jihye Yun4.   

Abstract

Over the past century, the notion that vitamin C can be used to treat cancer has generated much controversy. However, new knowledge regarding the pharmacokinetic properties of vitamin C and recent high-profile preclinical studies have revived interest in the utilization of high-dose vitamin C for cancer treatment. Studies have shown that pharmacological vitamin C targets many of the mechanisms that cancer cells utilize for their survival and growth. In this Opinion article, we discuss how vitamin C can target three vulnerabilities many cancer cells share: redox imbalance, epigenetic reprogramming and oxygen-sensing regulation. Although the mechanisms and predictive biomarkers that we discuss need to be validated in well-controlled clinical trials, these new discoveries regarding the anticancer properties of vitamin C are promising to help identify patient populations that may benefit the most from high-dose vitamin C therapy, developing effective combination strategies and improving the overall design of future vitamin C clinical trials for various types of cancer.

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Year:  2019        PMID: 30967651      PMCID: PMC6526932          DOI: 10.1038/s41568-019-0135-7

Source DB:  PubMed          Journal:  Nat Rev Cancer        ISSN: 1474-175X            Impact factor:   60.716


  140 in total

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Review 9.  Human genetic variation influences vitamin C homeostasis by altering vitamin C transport and antioxidant enzyme function.

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Review 7.  Metabolic Classification and Intervention Opportunities for Tumor Energy Dysfunction.

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8.  Clinical Targeting of Altered Metabolism in High-Grade Glioma.

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9.  Drug Repurposing of Pantoprazole and Vitamin C Targeting Tumor Microenvironment Conditions Improves Anticancer Effect in Metastatic Castration-Resistant Prostate Cancer.

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10.  Vitamin C Cytotoxicity and Its Effects in Redox Homeostasis and Energetic Metabolism in Papillary Thyroid Carcinoma Cell Lines.

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