Institute of Pathology, University of Regensburg, Regensburg, Germany.
Exp Dermatol. 2013 Apr;22(4):284-9. doi: 10.1111/exd.12127.
Over the past few years, the application of cold atmospheric plasma (CAP) in medicine has developed into an innovative field of research of rapidly growing importance. One promising new medical application of CAP is cancer treatment. Different studies revealed that CAP may potentially affect the cell cycle and cause cell apoptosis or necrosis in tumor cells dependent on the CAP device and doses. In this study, we used a novel hand-held and battery-operated CAP device utilizing the surface micro discharge (SMD) technology for plasma production in air and consequently analysed dose-dependent CAP treatment effects on melanoma cells. After 2 min of CAP treatment, we observed irreversible cell inactivation. Phospho-H2AX immunofluorescence staining and Flow cytometric analysis demonstrated that 2 min of CAP treatment induces DNA damage, promotes induction of Sub-G1 phase and strongly increases apoptosis. Further, protein array technology revealed induction of pro-apoptotic events like p53 and Rad17 phosphorylation of Cytochrome c release and activation of Caspase-3. Interestingly, using lower CAP doses with 1 min of treatment, almost no apoptosis was observed but long-term inhibition of proliferation. H3K9 immunofluorescence, SA-ß-Gal staining and p21 expression revealed that especially these low CAP doses induce senescence in melanoma cells. In summary, we observed differences in induction of apoptosis or senescence of tumor cells in respond to different CAP doses using a new CAP device. The mechanism of senescence with regard to plasma therapy was so far not described previously and is of great importance for therapeutic application of CAP.
在过去的几年中,冷等离子体(CAP)在医学中的应用已经发展成为一个具有重要意义的创新研究领域。CAP 的一个有前途的新医学应用是癌症治疗。不同的研究表明,CAP 可能会潜在地影响细胞周期,并根据 CAP 设备和剂量导致肿瘤细胞凋亡或坏死。在这项研究中,我们使用了一种新型的手持式和电池供电的 CAP 设备,利用表面微放电(SMD)技术在空气中产生等离子体,随后分析了剂量依赖性 CAP 处理对黑素瘤细胞的影响。经过 2 分钟的 CAP 处理,我们观察到了不可逆转的细胞失活。磷酸化 H2AX 免疫荧光染色和流式细胞术分析表明,2 分钟的 CAP 处理会诱导 DNA 损伤,促进 Sub-G1 期的诱导,并强烈增加细胞凋亡。此外,蛋白质阵列技术显示了促凋亡事件的诱导,如 p53 和 Rad17 的磷酸化、细胞色素 c 的释放和 Caspase-3 的激活。有趣的是,使用 1 分钟的较低 CAP 剂量,几乎观察不到细胞凋亡,但长期抑制增殖。H3K9 免疫荧光、SA-ß-Gal 染色和 p21 表达显示,这些低 CAP 剂量尤其会诱导黑素瘤细胞衰老。总之,我们观察到使用新型 CAP 设备,不同 CAP 剂量诱导肿瘤细胞凋亡或衰老的差异。关于等离子体治疗的衰老机制以前没有被描述过,这对 CAP 的治疗应用具有重要意义。