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Induction of Oxidative Stress in Tumor Cells: A New Strategy for Drug Therapy of Malignant Tumors

机译:肿瘤细胞氧化应激的诱导:恶性肿瘤药物治疗的新策略

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Abstract—Tumor cells have a higher basal ROS level than normal cells. This phenomenon may provide grounds for the development of novel antitumor drugs that are capable of selectively inducing oxidative stress in tumor cells. This approach can involve agents that induce ROS production and/or inhibit cellular enzymatic antioxidant systems. Thioredoxin reductase is a key enzyme in such systems. Overexpression of thioredoxin reductase has been shown in several types of tumors of hematopoietic, lymphoid, and other tissues. The results of studies of the antitumor activities of various synthetic and natural substances that are able to inhibit thioredoxin reductase are summarized. It is shown that thioredoxin reductase inhibition results in an increase in ROS level in tumor cells and oxidative damage of cells followed by apoptosis mainly via the mitochondrial pathway.
机译:摘要肿瘤细胞具有比正常细胞更高的基础ROS水平。 这种现象可以提供用于开发能够在肿瘤细胞中选择性地诱导氧化应激的新型抗肿瘤药物的基础。 该方法可以涉及诱导ROS产生和/或抑制细胞酶促抗氧化系统的药剂。 硫昔林还原酶是这种系统中的关键酶。 硫化辛还原酶的过度表达已被显示为造血,淋巴和其他组织的几种类型。 总结了能够抑制硫氧化酶还原酶的各种合成和天然物质的抗肿瘤活性的研究结果。 结果表明,毒素还原酶抑制导致肿瘤细胞中的ROS水平和细胞的氧化损伤,然后主要通过线粒体途径随后进行细胞凋亡。

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