Chen Zhiqiang, Wen Jian, Ju Huixiang, Fang Zheng
a Chemistry and Chemical Engineering College, Central South University , Changsha , China and.
b The Second Hospital Affiliated to Medical College, South East University , Nanjing , China.
Electromagn Biol Med. 2015;34(4):309-16. doi: 10.3109/15368378.2014.919589. Epub 2014 May 23.
Magnetic nano-Fe3O4 particles (MNPs), static magnetic field (SMF) and extremely low-frequency altering electric magnetic field (ELFF) were utilized to treat nude mice loading hepatoma Bel-7402 cell lines to investigate the therapeutic values of MNPs combined with ELFF in vivo. Magnetic resonance image (MRI) figures showed that about 98.9% MNPs injected into mice body through tail vein were gathered in tumor focal by SMF directing exposure. Single ELFF and MNPs treatments did not influence mice physiological function obviously. However, gathered MNPs combined with ELFF treatment prolonged mice survival time and inhibited loading tumor cells proliferation significantly compared to other mice groups (p < 0.05); furthermore, the tumor cells early apoptosis ratio of mice group was significantly higher than other groups (p < 0.05), and ELFF combined with gathered MNPs treatment improved tumor cells early apoptosis associated with Bcl group protein expression: Bax protein expression was higher than Bcl-2 and the combined treatment improved cells Heat shock protein-27 (Hsp-27) expression which could protect cells avoiding early apoptosis. The possible mechanism that this kind of combination inducing more cells into early apoptosis could be due to ELFF exposure influencing cells ion metabolism, MNPs strengthening the effects, and the ELFF vibrating MNPs to generate extra heat and activate cellular heat shock signal channel.
利用磁性纳米Fe3O4颗粒(MNPs)、静磁场(SMF)和极低频交变电磁场(ELFF)对接种肝癌Bel-7402细胞系的裸鼠进行治疗,以研究MNPs联合ELFF在体内的治疗价值。磁共振成像(MRI)图像显示,通过尾静脉注入小鼠体内的MNPs约98.9%在SMF定向暴露下聚集在肿瘤病灶处。单独的ELFF和MNPs治疗对小鼠生理功能无明显影响。然而,与其他小鼠组相比,聚集的MNPs联合ELFF治疗延长了小鼠存活时间并显著抑制了接种肿瘤细胞的增殖(p<0.05);此外,该小鼠组肿瘤细胞早期凋亡率显著高于其他组(p<0.05),且ELFF联合聚集的MNPs治疗改善了与Bcl家族蛋白表达相关的肿瘤细胞早期凋亡:Bax蛋白表达高于Bcl-2,联合治疗提高了细胞热休克蛋白27(Hsp-27)的表达,其可保护细胞避免早期凋亡。这种联合诱导更多细胞进入早期凋亡的可能机制可能是ELFF暴露影响细胞离子代谢,MNPs增强其作用,以及ELFF使MNPs振动产生额外热量并激活细胞热休克信号通道。