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Altered Antioxidant System Stimulates Dielectric Barrier Discharge Plasma-Induced Cell Death for Solid Tumor Cell Treatment

机译:改变的抗氧化剂系统刺激介电屏障放电血浆诱导的固体肿瘤细胞治疗细胞死亡。

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摘要

This study reports the experimental findings and plasma delivery approach developed at the Plasma Bioscience Research Center, Korea for the assessment of antitumor activity of dielectric barrier discharge (DBD) for cancer treatment. Detailed investigation of biological effects occurring after atmospheric pressure non-thermal (APNT) plasma application during in vitro experiments revealed the role of reactive oxygen species (ROS) in modulation of the antioxidant defense system, cellular metabolic activity, and apoptosis induction in cancer cells. To understand basic cellular mechanisms, we investigated the effects of APNT DBD plasma on antioxidant defense against oxidative stress in various malignant cells as well as normal cells. T98G glioblastoma, SNU80 thyroid carcinoma, KB oral carcinoma and a non-malignant HEK293 embryonic human cell lines were treated with APNT DBD plasma and cellular effects due to reactive oxygen species were observed. Plasma significantly decreased the metabolic viability and clonogenicity of T98G, SNU80, KB and HEK293 cell lines. Enhanced ROS in the cells led to death via alteration of total antioxidant activity, and NADP+/NADPH and GSH/GSSG ratios 24 hours (h) post plasma treatment. This effect was confirmed by annexin V-FITC and propidium iodide staining. These consequences suggested that the failure of antioxidant defense machinery, with compromised redox status, might have led to sensitization of the malignant cells. These findings suggest a promising approach for solid tumor therapy by delivering a lethal dose of APNT plasma to tumor cells while sparing normal healthy tissues.
机译:这项研究报告了韩国等离子生物科学研究中心开发的实验结果和血浆输送方法,用于评估介电屏障放电(DBD)的抗肿瘤活性以治疗癌症。在体外实验中大气压非热(APNT)等离子体施加后发生的生物学效应的详细研究揭示了活性氧(ROS)在调节抗氧化剂防御系统,细胞代谢活性和诱导癌细胞凋亡中的作用。为了了解基本的细胞机制,我们研究了APNT DBD血浆对各种恶性细胞以及正常细胞中抗氧化应激的抗氧化剂防御作用。用APNT DBD血浆处理T98G胶质母细胞瘤,SNU80甲状腺癌,KB口腔癌和非恶性HEK293胚胎人类细胞系,并观察到由于活性氧引起的细胞作用。血浆显着降低了T98G,SNU80,KB和HEK293细胞系的代谢活力和克隆形成能力。血浆处理后24小时(h),细胞中活性氧(ROS)的增加通过总抗氧化剂活性的改变以及NADP + / NADPH和GSH / GSSG比的改变而导致死亡。膜联蛋白V-FITC和碘化丙啶染色证实了该作用。这些结果表明,抗氧化防御机制的失败以及氧化还原状态的受损,可能导致了恶性细胞的致敏。这些发现提出了通过向致癌细胞递送致死剂量的APNT血浆同时保留正常健康组织的方法来进行实体瘤治疗的有希望的方法。

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