多任务分子维生素C发现杀死癌细胞的分子靶标

Robert Li
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引用次数: 11

摘要

两次诺贝尔奖得主莱纳斯·鲍林(Linus Pauling)在20世纪70年代的早期工作中,提出了使用大剂量维生素C治疗癌症患者的建议。在过去的几十年里,大量的动物模型研究以及一些小规模的临床研究为Linus Pauling的早期建议提供了大量的支持。通过维生素C的氧化产生活性氧(ROS)似乎是一个主要的潜在事件,导致选择性杀死癌细胞。然而,目前尚不清楚维生素C是如何选择性地杀死癌细胞而不伤害正常细胞的,以及高剂量维生素C的分子靶点是什么。在最近发表于《科学》杂志(2015年12月11日)的一篇文章中;350(6266): 1391 - 6。doi: 10.1126/science.aaa5004), Yun等报道维生素C通过ros依赖机制靶向甘油醛3-磷酸脱氢酶(GAPDH)选择性杀死KRAS和BRAF突变型结直肠癌细胞。Yun等人的这项工作以及其他发现推进了我们目前对高剂量维生素C介导的癌细胞杀伤的分子基础的理解,这可能会推动持续的研究努力,旨在进一步破译维生素C的新生物化学及其在癌症治疗中的独特作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Vitamin C, a Multi-Tasking Molecule, Finds a Molecular Target in Killing Cancer Cells.

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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