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通过冷大气等离子体的非侵入性应用在体外和体内增强替莫唑胺对人胶质母细胞瘤的疗效

In Vitro and In Vivo Enhancement of Temozolomide Effect in Human Glioblastoma by Non-Invasive Application of Cold Atmospheric Plasma.

作者信息

Soni Vikas, Adhikari Manish, Simonyan Hayk, Lin Li, Sherman Jonathan H, Young Colin N, Keidar Michael

机构信息

Department of Mechanical and Aerospace Engineering, MPNL, The George Washington University, Washington, DC 20052, USA.

Department of Pharmacology and Physiology, School of Medicine and Health Sciences, The George Washington University, Washington, DC 20052, USA.

出版信息

Cancers (Basel). 2021 Sep 6;13(17):4485. doi: 10.3390/cancers13174485.

Abstract

Glioblastoma (GBM) is one of the most aggressive forms of adult brain cancers and is highly resistant to treatment, with a median survival of 12-18 months after diagnosis. The poor survival is due to its infiltrative pattern of invasion into the normal brain parenchyma, the diffuse nature of its growth, and its ability to quickly grow, spread, and relapse. Temozolomide is a well-known FDA-approved alkylating chemotherapy agent used for the treatment of high-grade malignant gliomas, and it has been shown to improve overall survival. However, in most cases, the tumor relapses. In recent years, CAP has been used as an emerging technology for cancer therapy. The purpose of this study was to implement a combination therapy of CAP and TMZ to enhance the effect of TMZ and apparently sensitize GBMs. In vitro evaluations in TMZ-sensitive and resistant GBM cell lines established a CAP chemotherapy enhancement and potential sensitization effect across various ranges of CAP jet application. This was further supported with in vivo findings demonstrating that a single CAP jet applied non-invasively through the skull potentially sensitizes GBM to subsequent treatment with TMZ. Gene functional enrichment analysis further demonstrated that co-treatment with CAP and TMZ resulted in a downregulation of cell cycle pathway genes. These observations indicate that CAP can be potentially useful in sensitizing GBM to chemotherapy and for the treatment of glioblastoma as a non-invasive translational therapy.

摘要

胶质母细胞瘤(GBM)是成人脑癌中侵袭性最强的形式之一,对治疗具有高度抗性,诊断后的中位生存期为12至18个月。生存率低是由于其浸润性侵入正常脑实质的模式、生长的弥漫性以及快速生长、扩散和复发的能力。替莫唑胺是一种经美国食品药品监督管理局(FDA)批准的著名烷化剂化疗药物,用于治疗高级别恶性胶质瘤,已被证明可提高总生存期。然而,在大多数情况下,肿瘤会复发。近年来,电容耦合等离子体(CAP)已被用作一种新兴的癌症治疗技术。本研究的目的是实施CAP与替莫唑胺(TMZ)的联合治疗,以增强TMZ的效果并明显使GBM敏感化。在TMZ敏感和耐药的GBM细胞系中进行的体外评估确定了在不同范围的CAP射流应用中CAP化疗增强和潜在的敏感化作用。体内研究结果进一步支持了这一点,表明通过颅骨非侵入性施加单次CAP射流可能使GBM对随后的TMZ治疗敏感。基因功能富集分析进一步表明,CAP与TMZ联合治疗导致细胞周期途径基因下调。这些观察结果表明,CAP作为一种非侵入性转化疗法,在使GBM对化疗敏感以及治疗胶质母细胞瘤方面可能具有潜在用途。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b40/8430547/86aa7925d53b/cancers-13-04485-g001.jpg

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