关于维生素C(抗坏血酸钠)和K3(美萘醌)联合作为癌症辅助疗法潜在应用的新见解

J. Verrax, S. Bollen, M. Delvaux, H. Taper, P. Calderon
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引用次数: 3

摘要

癌症的特征是细胞周期失调、细胞分化逐渐丧失和生长失控。由于癌细胞对氧化应激特别敏感,我们利用这种较差的抗氧化状态,开发了一种实验方法,选择性地将癌细胞暴露于维生素C和K3 (CK3)相关诱导的氧化损伤中。无论在体内还是体外条件下,我们获得的结果都强化了氧化应激作为CK3杀伤细胞的主要机制的主要作用。这种抗肿瘤活性归因于维生素的氧化还原循环以及可能产生的过氧化物和其他活性氧。我们在此报告抗坏血酸与几种醌衍生物(具有不同的还原电位)的关联导致细胞死亡的能力。最后,我们确定CK3导致的细胞死亡与MAP激酶通路的激活无关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
New insights about the potential application of the association of vitamins C (sodium ascorbate) and K3 (menadione) as auxiliary therapy in cancer treatment
Cancer is characterized by cell cycle deregulation, progressive loss of cell differentiation and uncontrolled growth. Since cancer cells are particulary sensitive to oxidative stress, we took advantage of this poor antioxidant status to develop an experimental approach to selectively expose cancer cells to an oxidant insult induced by the association of vitamins C and K3 (CK3). The results we obtained reinforce the major role of oxidative stress as the main mechanism involved in cell killing by CK3, either under in vivo or in vitro conditions. such an antitumor activity has been attributed to redox cycling of the vitamins and the possible generation of peroxides and other reactive oxygen species. We report herein, on the ability of the association of ascorbate with several quinone derivatives (having differentredox potentials) to cause cell death. Finally, we determined that cell death by CK3 is not related to the activation of MAP kinases pathways.
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