Treatment of glioblastoma with tumor-specific amplitude-modulated radiofrequency electromagnetic fields.

Q2 Medicine
Hugo Jimenez, Denise Gibo, Sambad Sharma, Michael Pennison, Lance D Miller, Minghui Wang, Kimberly Sheffield, Liyue Zhang, Allan Johansen, Preeya Achari, Callum Mcgrath, Sean Lester, Jason Tang, Kojo Agyemang, Annette Johnson, Christopher T Whitlow, Michael Chan, Kounosuke Watabe, Ralph D'Agostino, Janaka Liyanage, Asfar Azmi, Geoffrey Barger, Alexandre Barbault, Glenn J Lesser, Waldemar Debinski, Boris C Pasche
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引用次数: 0

Abstract

Background: Intrabuccal administration of amplitude-modulated 27.12 MHz radiofrequency electromagnetic fields (AM RF EMF) resulting in the systemic delivery of low and safe levels of AM RF EMF has shown activity in several forms of cancer.

Methods: Glioblastoma (GB) cell lines were exposed to GB-specific AM RF EMF (GBMF) three hours per day at a level of exposure identical to patients during treatment. Cellular assays and agnostic genomic approaches were used to characterize the mechanism-of-action. One patient with therapy refractory GB received compassionate use treatment with GBMF as well as a second patient with refractory oligodendroglioma.

Results: Treatment with GBMF inhibited the proliferation of several GB cell lines. CACNA1H mediates the effect of GBMF. GBMF modulates the "Mitotic Roles of Polo-Like Kinase" pathway resulting in the disruption of GB mitotic spindle. There was evidence of clinical and radiological benefit in a 38-year-old patient with recurrent GB and evidence of safety and feasibility in a 47-year-old patient with oligodendroglioma.

Conclusions: This is the first report showing in vitro antitumor activity, disruption of the mitotic spindle, activation of the Mitotic Roles of Polo-like kinase pathway in GB. This is also the first report showing feasibility and clinical activity in patients with brain tumor.

肿瘤特异性调幅射频电磁场治疗胶质母细胞瘤。
背景:经调幅27.12 MHz射频电磁场(AM RF EMF)的颊内管理导致低安全水平的AM RF EMF的全身输送,已显示出对几种形式的癌症的活性。方法:胶质母细胞瘤(GB)细胞系每天暴露于GB特异性AM RF EMF (GBMF) 3小时,暴露水平与治疗期间患者相同。细胞测定和不可知论的基因组方法被用来表征作用机制。一名难治性GB患者接受GBMF同情治疗,另一名难治性少突胶质细胞瘤患者接受GBMF同情治疗。结果:GBMF抑制了几种GB细胞系的增殖。CACNA1H介导GBMF的作用。GBMF调节“polo样激酶的有丝分裂作用”通路,导致GB有丝分裂纺锤体的破坏。有证据表明,38岁复发GB患者的临床和放射学获益,以及47岁少突胶质细胞瘤患者的安全性和可行性。结论:这是第一个在GB中显示出体外抗肿瘤活性,破坏有丝分裂纺锤体,激活polo样激酶途径的有丝分裂作用的报道。这也是首个在脑肿瘤患者中显示可行性和临床活性的报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Oncotarget
Oncotarget Oncogenes-CELL BIOLOGY
CiteScore
6.60
自引率
0.00%
发文量
129
审稿时长
1.5 months
期刊介绍: Information not localized
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