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10.20455/ros.2016.829

http://scihub22266oqcxt.onion/10.20455/ros.2016.829
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C5959041!5959041!29780883
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suck abstract from ncbi


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pmid29780883      React+Oxyg+Species+(Apex) 2016 ; 1 (2): 141-56
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  • Vitamin C, a Multi-Tasking Molecule, Finds a Molecular Target in Killing Cancer Cells #MMPMID29780883
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  • React Oxyg Species (Apex) 2016[Mar]; 1 (2): 141-56 PMID29780883show ga
  • Early work in the 1970s by Linus Pauling, a twice-honored Nobel laureate, led to his proposal of using high-dose vitamin C to treat cancer patients. Over the past several decades, a number of studies in animal models as well as several small-scale clinical studies have provided substantial support of Linus Pauling?s early proposal. Production of reactive oxygen species (ROS) via oxidation of vitamin C appears to be a major underlying event, leading to the selective killing of cancer cells. However, it remains unclear how vitamin C selectively kills cancer cells while sparing normal cells and what the molecular targets of high-dose vitamin C are. In a recent article published in Science (2015 December 11; 350(6266):1391?6. doi: 10.1126/science.aaa5004), Yun et al. reported that vitamin C selectively kills KRAS and BRAF mutant colorectal cancer cells by targeting glyceraldehyde 3-phosphate dehydrogenase (GAPDH) through an ROS-dependent mechanism. This work by Yun et al. along with other findings advances our current understanding of the molecular basis of high-dose vitamin C-mediated cancer cell killing, which will likely give an impetus to the continued research efforts aiming to further decipher the novel biochemistry of vitamin C and its unique role in cancer therapy.
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