Tumor suppressive effect of low-frequency repetitive transcranial magnetic stimulation on glioblastoma progression

IF 6.9 2区 医学 Q1 CLINICAL NEUROLOGY Neurotherapeutics Pub Date : 2025-07-01 Epub Date: 2025-03-27 DOI:10.1016/j.neurot.2025.e00569
Seongmoon Jo , Sang Hee Im , Sung Hoon Kim , Dawoon Baek , Jin-Kyoung Shim , Seok-Gu Kang , Jong Hee Chang , Geneva Rose Notario , Do-Won Lee , Ahreum Baek , Sung-Rae Cho
{"title":"Tumor suppressive effect of low-frequency repetitive transcranial magnetic stimulation on glioblastoma progression","authors":"Seongmoon Jo ,&nbsp;Sang Hee Im ,&nbsp;Sung Hoon Kim ,&nbsp;Dawoon Baek ,&nbsp;Jin-Kyoung Shim ,&nbsp;Seok-Gu Kang ,&nbsp;Jong Hee Chang ,&nbsp;Geneva Rose Notario ,&nbsp;Do-Won Lee ,&nbsp;Ahreum Baek ,&nbsp;Sung-Rae Cho","doi":"10.1016/j.neurot.2025.e00569","DOIUrl":null,"url":null,"abstract":"<div><div>Repetitive transcranial magnetic stimulation (rTMS) is used as a non-invasive treatment for various diseases, and its potential application in cancer treatment has been proposed by researchers. However, the precise mechanisms and effects of rTMS on many types of cancer, including glioblastoma (GBM), remain largely unknown. This study aimed to investigate the effects of low-frequency rTMS on <em>in vitro</em> and <em>in vivo</em> GBM models and to elucidate an underlying biological mechanism of rTMS on GBM. <em>In vitro</em> and <em>in vivo</em> GBM models were treated with low-frequency rTMS (0.5 ​Hz, 10 ​min per day), and the effects of rTMS were assessed using various assays, including CCK-8 assay, sphere formation assay, 3D invasion assay, RT-qPCR, Western blot, immunohistochemistry, TUNEL assay, MRI, and IVIS. The results showed that treatment of GBM models <em>in vitro</em> with low-frequency rTMS significantly inhibited cell proliferation. Transcriptome array analysis revealed a substantial downregulation of FLNA and FLNC expression after low-frequency rTMS treatment. Moreover, in an <em>in vitro</em> GBM tumor sphere model, low-frequency rTMS suppressed the activation of EGFR and EphA2, inhibited ERK/JNK/p38 and PI3K/AKT/mTOR pathways, and induced apoptosis. Low-frequency rTMS also suppressed the invasion of GBM by downregulating MMP2 and MMP9 expression. Additionally, in an <em>in vivo</em> GBM model, low-frequency rTMS suppressed GBM progression by downregulating FLNA and FLNC expression. The results demonstrated that low-frequency rTMS could be a potential treatment for GBM, achieved by downregulating FLNA and FLNC expression. This study sheds light on the potential for rTMS as a therapeutic strategy for glioblastoma as well as other types of cancers.</div></div>","PeriodicalId":19159,"journal":{"name":"Neurotherapeutics","volume":"22 4","pages":"Article e00569"},"PeriodicalIF":6.9000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Neurotherapeutics","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1878747925000479","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/3/27 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Repetitive transcranial magnetic stimulation (rTMS) is used as a non-invasive treatment for various diseases, and its potential application in cancer treatment has been proposed by researchers. However, the precise mechanisms and effects of rTMS on many types of cancer, including glioblastoma (GBM), remain largely unknown. This study aimed to investigate the effects of low-frequency rTMS on in vitro and in vivo GBM models and to elucidate an underlying biological mechanism of rTMS on GBM. In vitro and in vivo GBM models were treated with low-frequency rTMS (0.5 ​Hz, 10 ​min per day), and the effects of rTMS were assessed using various assays, including CCK-8 assay, sphere formation assay, 3D invasion assay, RT-qPCR, Western blot, immunohistochemistry, TUNEL assay, MRI, and IVIS. The results showed that treatment of GBM models in vitro with low-frequency rTMS significantly inhibited cell proliferation. Transcriptome array analysis revealed a substantial downregulation of FLNA and FLNC expression after low-frequency rTMS treatment. Moreover, in an in vitro GBM tumor sphere model, low-frequency rTMS suppressed the activation of EGFR and EphA2, inhibited ERK/JNK/p38 and PI3K/AKT/mTOR pathways, and induced apoptosis. Low-frequency rTMS also suppressed the invasion of GBM by downregulating MMP2 and MMP9 expression. Additionally, in an in vivo GBM model, low-frequency rTMS suppressed GBM progression by downregulating FLNA and FLNC expression. The results demonstrated that low-frequency rTMS could be a potential treatment for GBM, achieved by downregulating FLNA and FLNC expression. This study sheds light on the potential for rTMS as a therapeutic strategy for glioblastoma as well as other types of cancers.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
低频重复经颅磁刺激对胶质母细胞瘤进展的抑制作用。
重复经颅磁刺激(rTMS)被用作治疗各种疾病的非侵入性疗法,研究人员也提出了其在癌症治疗中的潜在应用。然而,经颅磁刺激对包括胶质母细胞瘤(GBM)在内的多种癌症的确切机制和影响在很大程度上仍然未知。本研究旨在探讨低频经颅磁刺激对体外和体内 GBM 模型的影响,并阐明经颅磁刺激对 GBM 的潜在生物学机制。采用低频经颅磁刺激(0.5赫兹,每天10分钟)对体外和体内GBM模型进行治疗,并使用多种检测方法评估经颅磁刺激的效果,包括CCK-8检测、球形成检测、三维侵袭检测、RT-qPCR、Western印迹、免疫组化、TUNEL检测、MRI和IVIS。结果表明,用低频经颅磁刺激治疗体外 GBM 模型可显著抑制细胞增殖。转录组阵列分析显示,低频经颅磁刺激处理后,FLNA和FLNC的表达大幅下调。此外,在体外 GBM 肿瘤球模型中,低频经颅磁刺激抑制了表皮生长因子受体(EGFR)和表皮生长因子受体(EphA2)的活化,抑制了 ERK/JNK/p38 和 PI3K/AKT/mTOR 通路,并诱导了细胞凋亡。低频经颅磁刺激还能通过下调 MMP2 和 MMP9 的表达来抑制 GBM 的侵袭。此外,在体内 GBM 模型中,低频经颅磁刺激通过下调 FLNA 和 FLNC 的表达抑制了 GBM 的进展。研究结果表明,低频经颅磁刺激可以通过下调 FLNA 和 FLNC 的表达来治疗 GBM。这项研究揭示了经颅磁刺激作为胶质母细胞瘤和其他类型癌症治疗策略的潜力。
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 去求助
来源期刊
Neurotherapeutics
Neurotherapeutics 医学-神经科学
CiteScore
11.00
自引率
3.50%
发文量
154
审稿时长
6-12 weeks
期刊介绍: Neurotherapeutics® is the journal of the American Society for Experimental Neurotherapeutics (ASENT). Each issue provides critical reviews of an important topic relating to the treatment of neurological disorders written by international authorities. The Journal also publishes original research articles in translational neuroscience including descriptions of cutting edge therapies that cross disciplinary lines and represent important contributions to neurotherapeutics for medical practitioners and other researchers in the field. Neurotherapeutics ® delivers a multidisciplinary perspective on the frontiers of translational neuroscience, provides perspectives on current research and practice, and covers social and ethical as well as scientific issues.
期刊最新文献
Current and emerging therapies in IDH-mutant glioma Pulsed focused ultrasound for seizure suppression: Mechanisms, models, and clinical translation Sex-specific considerations in migraine therapy. Investigations of remibrutinib in models pertinent to multiple sclerosis. A phase 1, safety, tolerability, and pharmacokinetics study of bisnorcymserine, a highly selective inhibitor of butyrylcholinesterase.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1