结合冷物理等离子体与脉冲电场治疗癌症

Q1 Medicine
Christina Maria Wolff, Anna Steuer, Jürgen F. Kolb, Sander Bekeschus
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引用次数: 0

摘要

晚期黑色素瘤和乳腺癌患者的缓解是一个挑战。尽管在这些患者中普遍成功地使用了电化疗(ECT),但反应率仍然可以提高。先前的研究证明了纳米秒PEFs (nsPEFs)的抗癌潜力,在不同的设置下,它能够诱导细胞凋亡[1]或纳米孔的形成[2]。同样,冷物理等离子体的抗癌能力已在细胞系和小鼠异种移植肿瘤的各种研究中得到证实[3-7]。冷等离子体的凋亡效应是由多种活性物质释放到细胞上介导的,这些活性物质触发氧化还原信号,在某些情况下导致细胞死亡[8,9]。相比之下,pef的作用机制较少依赖于新产生的反应物质。我们的想法是将这两种治疗方法结合起来,以改善未来的姑息性癌症治疗。我们对恶性悬浮细胞系进行了试验,以证实其具有附加性甚至可能的协同细胞毒作用。改变血浆治疗时间(kINPen)和PEF强度以及脉冲长度,以获取每次治疗的亚致死剂量方案。组合的顺序(首先是等离子体,然后是PEF,反之亦然)也被调制。为了研究这两种疗法的作用方式,研究了许多细胞参数。这包括细胞质和膜室的氧化、硫醇含量、线粒体去极化、半胱天冬酶激活和磷脂酰丝氨酸暴露、代谢活性、细胞膜通透性、细胞生长和形态以及抗氧化剂的保护作用。此外,我们在初步试验中使用致瘤贴壁细胞确定了血浆和pef的协同作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combining cold physical plasma with pulsed electrical fields for cancer treatment

Pallation of end-stage melanoma and breast cancer patients is a challenge. Despite the generally successful use of electrochemotherapy (ECT) in these patients, response rates can still be improved. Previous studies demonstrated the anticancer potential of nano-second PEFs (nsPEFs), which are able to induce apoptosis [1] or nanopore formation when using different settings [2]. Likewise, the anticancer capacity of cold physical plasma has been demonstrated in various studies in cell lines and in xenograft tumors in mice [3-7]. The apoptotic effect of cold plasmas is mediated by a variety of reactive species being released onto the cells, where the species trigger redox signaling, and subsequent cell death in some instances [8, 9]. By contrast, PEFs act by a mechanism much less dependent on the newly generated reactive species. Our idea was to combine both treatments to improve palliative cancer treatment in the future.

Malignant suspension cell lines were tested to investigate the proof of concept of additive or possible even synergistic cytotoxic effects. Plasma treatment time (kINPen) and PEF intensity as well as pulse length were varied to retrieve sublethal dosage regimens for each treatment. The sequence of combination (first plasma, then PEF or vice versa) was also modulated. To investigate the mode of action of both therapies, a number of cellular parameters were investigated. This included oxidation at cytosolic and membrane compartments, thiol content, mitochondrial depolarization, caspase activation and phosphatidylserine exposure, metabolic activity, cell membrane permeabilization, cell growth and morphology, and protection by antioxidants. Furthermore, we identified a synergistic effect of plasma and PEFs using tumorigenic adherent cells in preliminary tests.

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来源期刊
Clinical Plasma Medicine
Clinical Plasma Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
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