Adaptation Of Operational Parameters Of Cold Atmospheric Plasma And Their Role In Cancer Therapy

Q1 Medicine
Eda Gjika , Sonali Pal-Ghosh , Li Lin , Gauri Tadvalkar , Zhitong Chen , Colin Young , Jerome Canady , Jonathan Sherman , Mary Ann Stepp , Michael Keidar
{"title":"Adaptation Of Operational Parameters Of Cold Atmospheric Plasma And Their Role In Cancer Therapy","authors":"Eda Gjika ,&nbsp;Sonali Pal-Ghosh ,&nbsp;Li Lin ,&nbsp;Gauri Tadvalkar ,&nbsp;Zhitong Chen ,&nbsp;Colin Young ,&nbsp;Jerome Canady ,&nbsp;Jonathan Sherman ,&nbsp;Mary Ann Stepp ,&nbsp;Michael Keidar","doi":"10.1016/j.cpme.2017.12.026","DOIUrl":null,"url":null,"abstract":"<div><p><span><span>The evaluation of CAP in cancer treatment has been significantly fueled by the growing demand for more effective therapies. CAP has been reported as a selective treatment method with a higher affinity of inducing </span>cell death in </span>cancer cells<span><span> while leaving normal cells unharmed. However, the extent of its effectiveness varies significantly per cancer type. Studies have revealed that different types of cancers exhibit different response to treatment when exposed to the same CAP conditions. Therefore, an understanding of the immediate effect of CAP on cancer cells may enable improvement of treatment outcomes [1]. We demonstrated that instantaneous CAP response can be monitored in real-time by RealTime-Glo Assay with results interpreted as </span>cell viability. This creates the possibility for developing an adaptive CAP approach platform which could enable real-time modification of the plasma treatment condition. In particular, the composition of reactive oxygen and nitrogen species (RONS) and the intensity of CAP, which is effected by discharge voltage and length of treatment, can be optimized with a feedback system at regular intervals to minimize the predicted viability of cancer cells [1, 2].</span></p><p>In an <em>in vitro</em><span> proof-of-concept study conducted in glioblastoma<span> and breast cancer cells, we showed that CAP reduced cell viability in a dose dependent manner as a function of treatment duration and plasma discharge voltage. In fact, a 30-60 second increase in treatment duration and/or a discharge voltage adjustment from 3.16 to 3.71 kV, was consistently accompanied with a significant reduction in cell viability. Therefore, these two operational parameters can be utilized for adjusting plasma composition and improving treatment outcomes. In addition to the cell viability findings, we determined that CAP inhibited cancer cell proliferation and triggered apoptosis via damage to the mitochondrial membrane<span> and deregulation of the protein synthesis mechanism [2]. The work completed in this study will serve as the foundation for the development of the adaptive CAP platform. The novel platform will intend to propel CAP therapy forefront other well-established therapies associated with cancer treatment.</span></span></span></p></div>","PeriodicalId":46325,"journal":{"name":"Clinical Plasma Medicine","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2018-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.cpme.2017.12.026","citationCount":"4","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Plasma Medicine","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2212816617300513","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 4

Abstract

The evaluation of CAP in cancer treatment has been significantly fueled by the growing demand for more effective therapies. CAP has been reported as a selective treatment method with a higher affinity of inducing cell death in cancer cells while leaving normal cells unharmed. However, the extent of its effectiveness varies significantly per cancer type. Studies have revealed that different types of cancers exhibit different response to treatment when exposed to the same CAP conditions. Therefore, an understanding of the immediate effect of CAP on cancer cells may enable improvement of treatment outcomes [1]. We demonstrated that instantaneous CAP response can be monitored in real-time by RealTime-Glo Assay with results interpreted as cell viability. This creates the possibility for developing an adaptive CAP approach platform which could enable real-time modification of the plasma treatment condition. In particular, the composition of reactive oxygen and nitrogen species (RONS) and the intensity of CAP, which is effected by discharge voltage and length of treatment, can be optimized with a feedback system at regular intervals to minimize the predicted viability of cancer cells [1, 2].

In an in vitro proof-of-concept study conducted in glioblastoma and breast cancer cells, we showed that CAP reduced cell viability in a dose dependent manner as a function of treatment duration and plasma discharge voltage. In fact, a 30-60 second increase in treatment duration and/or a discharge voltage adjustment from 3.16 to 3.71 kV, was consistently accompanied with a significant reduction in cell viability. Therefore, these two operational parameters can be utilized for adjusting plasma composition and improving treatment outcomes. In addition to the cell viability findings, we determined that CAP inhibited cancer cell proliferation and triggered apoptosis via damage to the mitochondrial membrane and deregulation of the protein synthesis mechanism [2]. The work completed in this study will serve as the foundation for the development of the adaptive CAP platform. The novel platform will intend to propel CAP therapy forefront other well-established therapies associated with cancer treatment.

低温大气等离子体操作参数的适应性及其在癌症治疗中的作用
对更有效的治疗方法的需求不断增长,极大地推动了CAP在癌症治疗中的评估。据报道,CAP是一种选择性治疗方法,具有较高的诱导癌细胞死亡而不伤害正常细胞的亲和力。然而,它的效力程度因癌症类型而有很大差异。研究表明,当暴露在相同的CAP条件下,不同类型的癌症对治疗表现出不同的反应。因此,了解CAP对癌细胞的直接作用可能有助于改善治疗结果[10]。我们证明瞬时CAP反应可以通过RealTime-Glo Assay实时监测,结果解释为细胞活力。这为开发一种自适应CAP方法平台创造了可能性,该平台可以实时修改等离子体处理条件。特别是,受放电电压和处理时间影响的活性氧和氮种(ron)的组成和CAP的强度,可以通过定期反馈系统进行优化,使预测的癌细胞生存能力最小化[1,2]。在一项对胶质母细胞瘤和乳腺癌细胞进行的体外概念验证研究中,我们发现CAP以剂量依赖的方式降低细胞活力,这是治疗时间和等离子体放电电压的函数。事实上,延长30-60秒的处理时间和/或将放电电压从3.16 kV调整到3.71 kV,始终伴随着细胞活力的显著降低。因此,这两个操作参数可用于调整血浆成分和改善治疗效果。除了细胞活力的发现外,我们还确定CAP通过损伤线粒体膜和解除蛋白质合成机制[2]来抑制癌细胞增殖并引发细胞凋亡。本研究完成的工作将为自适应CAP平台的开发奠定基础。这个新颖的平台将推动CAP治疗走在与癌症治疗相关的其他成熟疗法的前列。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Clinical Plasma Medicine
Clinical Plasma Medicine MEDICINE, RESEARCH & EXPERIMENTAL-
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信