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Vitamin C - A new player in regulation of the cancer epigenome

期刊

SEMINARS IN CANCER BIOLOGY
卷 51, 期 -, 页码 59-67

出版社

ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcancer.2017.11.001

关键词

Vitamin C; Epigenetics; Cancer treatment; Hematological malignancies; Ascorbic acid

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资金

  1. Danish Cancer Society
  2. Rigshospitalets Research Foundation
  3. Lundbeck Foundation
  4. Novo Nordisk Foundation
  5. National Institute of Health [R35CA209858]
  6. Van Andel Research Institute through the Van Andel Research Institute Stand Up To Cancer Epigenetics Dream Team
  7. NATIONAL CANCER INSTITUTE [R35CA209859] Funding Source: NIH RePORTER
  8. Lundbeck Foundation [R180-2014-3675] Funding Source: researchfish
  9. Novo Nordisk Fonden [NNF13OC0003435] Funding Source: researchfish
  10. The Danish Cancer Society [R124-A7695] Funding Source: researchfish
  11. Novo Nordisk Foundation Section for Basic Stem Cell Biology [Gr�nb�k group NNF] Funding Source: researchfish

向作者/读者索取更多资源

Over the past few years it has become clear that vitamin C, as a provider of reduced iron, is an essential factor for the function of epigenetic regulators that initiate the demethylation of DNA and histones. Vitamin C deficiency is rare in the general population, but is frequently observed in patients with cancer. Genes encoding epigenetic regulators are often mutated in cancer, underscoring their central roles in carcinogenesis. In hematological cancers, such as acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS), drugs that reverse epigenetic aberrations are now the standard of care. Recent in vitro studies suggest that vitamin C at physiological concentrations, combined with hypomethylating agents may act synergistically to cause DNA demethylation through active and passive mechanisms, respectively. Additionally, several recent studies have renewed interest in the use of pharmacological doses of vitamin C injected intravenously to selectively kill tumor cells. This review will focus on the potential of vitamin C to optimize the outcome of epigenetic therapy in cancer patients and alternatively to act as a therapeutic at high doses.

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