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Cold Atmospheric Plasma Treatment Induces Anti-Proliferative Effects in Prostate Cancer Cells by Redox and Apoptotic Signaling Pathways

机译:冷大气等离子体处理通过氧化还原和凋亡信号通路诱导前列腺癌细胞的抗增殖作用。

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摘要

One of the promising possibilities of the clinical application of cold plasma, so-called cold atmospheric plasma (CAP), is its application on malignant cells and cancer tissue using its anti-neoplastic effects, primarily through the delivery of reactive oxygen and nitrogen species (ROS, RNS). In this study, we investigated the impact of CAP on cellular proliferation and consecutive molecular response mechanisms in established prostate cancer (PC) cell lines. PC cells showed a significantly reduced cell growth following CAP treatment as a result of both an immediate increase of intracellular peroxide levels and through the induction of apoptosis indicated by annexin V assay, TUNEL assay, and the evaluation of changes in nuclear morphology. Notably, co-administration of N-acetylcysteine (NAC) completely neutralized CAP effects by NAC uptake and rapid conversion to glutathione (GSH). Vitamin C could not counteract the CAP induced effects on cell growth. In summary, relatively short treatments with CAP of 10 seconds were sufficient to induce a significant inhibition of cancer proliferation, as observed for the first time in urogenital cancer. Therefore, it is important to understand the mode of CAP related cell death and clarify and optimize CAP as cancer therapy. Increased levels of peroxides can alter redox-regulated signaling pathways and can lead to growth arrest and apoptosis. We assume that the general intracellular redox homeostasis, especially the levels of cellular GSH and peroxidases such as peroxiredoxins affect the outcome of the CAP treatment.
机译:冷血浆(所谓的冷大气血浆(CAP))的临床应用的有前途的可能性之一是其抗肿瘤作用主要通过释放活性氧和氮来实现其在恶性细胞和癌组织上的应用( ROS,RNS)。在这项研究中,我们调查了CAP对已建立的前列腺癌(PC)细胞系中细胞增殖和连续分子应答机制的影响。由于细胞内过氧化物水平的立即增加以及膜联蛋白V测定法,TUNEL测定法和评估核形态变化所指示的凋亡诱导,PC细胞在CAP处理后显示出明显减少的细胞生长。值得注意的是,N-乙酰半胱氨酸(NAC)的共同给药通过NAC吸收和快速转化为谷胱甘肽(GSH)完全中和了CAP的作用。维生素C不能抵消CAP诱导的细胞生长。总之,如在泌尿生殖道癌症中首次观察到的,用10秒的CAP进行相对短的治疗就足以诱导对癌症增殖的显着抑制。因此,重要的是要了解CAP相关的细胞死亡方式,并阐明和优化CAP作为癌症的治疗方法。过氧化物水平的增加可以改变氧化还原调节的信号通路,并可能导致生长停滞和细胞凋亡。我们假设一般的细胞内氧化还原稳态,尤其是细胞GSH和过氧化物酶(例如过氧化物氧还蛋白)的水平会影响CAP治疗的结果。

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