Different duration of exposure to a pulsed magnetic field can cause changes in mRNA expression of apoptotic genes in oleic acid-treated neuroblastoma cells.

Çiğdem Gökçek-Saraç, Ebru Çetin, Kayhan Ateş, Şükrü Özen, Serdar Karakurt
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Abstract

Purpose: Neuroblastoma, a prevalent childhood tumor, poses significant challenges in therapeutic interventions, especially for high-risk cases. This study aims to fill a crucial gap in our understanding of neuroblastoma treatment by investigating the potential molecular impacts of short- and long-term pulsed magnetic field exposure on the neuronal apoptosis mechanism in an in vitro model of neuroblastoma treated with oleic acid (OA).

Materials and methods: Cells were cultured and divided into six following experimental groups: (I) Nontreated group (NT); (II) OA-treated group (OA); (III) Group treated with OA after being exposed to the pulsed magnetic field for 15-min (15 min PEMF + OA); (IV) Group treated with OA after being exposed to the pulsed magnetic field for 12 h (12 h PEMF + OA); (V) Group exposed to the pulsed magnetic field for 15 min (15 min PEMF); and (VI) Group exposed to the pulsed magnetic field for 12 h (12 h PEMF). Cell viability, rates of apoptosis, and mRNA levels of key apoptotic genes (TP53, Bcl2, Bax, and Caspase-3) were assessed.

Results: Significant reductions in cell viability were observed, particularly in the group treated with OA following long-term pulsed magnetic field exposure. Flow cytometry revealed elevated apoptosis rates, notably in the early stages of apoptosis. qRT-PCR analysis demonstrated increased expression of cleaved Caspase-3, Bax/Bcl2 ratio, and TP53 in cells treated with OA following long-term pulsed magnetic field exposure, signifying enhanced apoptotic pathways.

Conclusions: The findings indicate that long-term pulsed magnetic field exposure and OA treatment exhibit potential synergistic effects leading to the induction of apoptosis in SH-SY5Y cells. We have concluded that stimulations of pulsed magnetic field have the potential to serve as an adjuvant therapy for oleic acid-based treatment of neuroblastoma.

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暴露于脉冲磁场的时间长短不同,会导致油酸处理过的神经母细胞瘤细胞中凋亡基因的 mRNA 表达发生变化。
目的:神经母细胞瘤是一种常见的儿童肿瘤,给治疗干预带来了巨大挑战,尤其是对高危病例。本研究旨在通过研究短期和长期脉冲磁场暴露对用油酸(OA)处理的神经母细胞瘤体外模型中神经细胞凋亡机制的潜在分子影响,填补我们对神经母细胞瘤治疗认识上的一个重要空白:将培养的细胞分为以下六个实验组:(I)未处理组(NT);(II)OA 处理组(OA);(III)暴露于脉冲磁场 15 分钟后用 OA 处理组(15 分钟 PEMF + OA);(IV) 在脉冲磁场中暴露 12 小时后再用 OA 处理的组(12 小时 PEMF + OA); (V) 在脉冲磁场中暴露 15 分钟后再用 OA 处理的组(15 分钟 PEMF);以及 (VI) 在脉冲磁场中暴露 12 小时后再用 OA 处理的组(12 小时 PEMF)。对细胞活力、凋亡率和主要凋亡基因(TP53、Bcl2、Bax 和 Caspase-3)的 mRNA 水平进行了评估:结果:观察到细胞存活率显著降低,尤其是在长期暴露于脉冲磁场后接受 OA 治疗的组别中。qRT-PCR 分析表明,长期暴露于脉冲磁场后,用 OA 处理的细胞中裂解的 Caspase-3、Bax/Bcl2 比率和 TP53 的表达增加,表明细胞凋亡途径增强:研究结果表明,长期脉冲磁场暴露和 OA 处理具有潜在的协同效应,可诱导 SH-SY5Y 细胞凋亡。我们得出结论,脉冲磁场刺激有可能成为基于油酸治疗神经母细胞瘤的辅助疗法。
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