Cadet Brigade, College of Basic Medicine, Air Force Medical University, Xi'an City, Shannxi Province, China.
State Key Laboratory of Cancer Biology, Department of Pathology, Xijing Hospital and School of Basic Medicine, Air Force Medical University, Xi'an City, Shannxi Province, China.
Bioelectromagnetics. 2024 Jul;45(5):218-225. doi: 10.1002/bem.22500. Epub 2024 Mar 27.
Mounting literature indicates that electromagnetic pulses (EMP) is the promising modality to treat cancers with advantages such as noninvasiveness and few side-effects, but its appropriate parameters and underlying mechanisms such as its influence on tumor-derived exosomes (TDEs) are largely unknown. This study aimed to elucidate effects of EMP, exosome inhibition and their coaction on A549 lung adenocarcinoma cells. A549 cells were randomly divided into control group, GW4869 group treated by 20 μM GW4869, vehicle group treated by dimethyl sulfoxide, EMP group treated by EMP exposure, and EMPG group treated by EMP exposure combined with 20 μM GW4869. After EMP exposure, cell proliferation was determined by CCK8 assay, cell cycle and apoptosis was detected by flow cytometry, and cell migration was determined by transwell assay. The results showed that EMP or exosomes inhibition did not affect cell proliferation, cell cycle, apoptosis and cell migration (p > 0.05), but cell migration in EMPG group was significantly decreased compared with vehicle group (p < 0.05). We concluded that under the experimental condition, EMP or GW4869 alone had no effects on behaviors of A549 cells, but their coaction could effectively inhibit the migration of A549 cells.
越来越多的文献表明,电磁脉冲 (EMP) 是一种很有前途的治疗癌症的方法,具有非侵入性和副作用少等优点,但它的适当参数和潜在机制,如对肿瘤衍生外泌体 (TDEs) 的影响,在很大程度上尚不清楚。本研究旨在阐明 EMP、外泌体抑制及其共同作用对 A549 肺腺癌细胞的影响。A549 细胞随机分为对照组、GW4869 组(用 20μM GW4869 处理)、溶剂组(用二甲基亚砜处理)、EMP 组(EMP 暴露处理)和 EMPG 组(EMP 暴露联合 20μM GW4869 处理)。EMP 暴露后,通过 CCK8 测定法测定细胞增殖,通过流式细胞术检测细胞周期和凋亡,通过 Transwell 测定法测定细胞迁移。结果表明,EMP 或外泌体抑制均不影响细胞增殖、细胞周期、凋亡和细胞迁移(p>0.05),但 EMPG 组的细胞迁移明显低于溶剂组(p<0.05)。我们得出结论,在实验条件下,单独的 EMP 或 GW4869 对 A549 细胞的行为没有影响,但它们的共同作用可以有效抑制 A549 细胞的迁移。