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Induction of apoptosis in cancer cells by NiZn ferrite nanoparticles through mitochondrial cytochrome C release

机译:NiZn铁氧体纳米粒通过线粒体细胞色素C释放诱导癌细胞凋亡

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摘要

The long-term objective of the present study was to determine the ability of NiZn ferrite nanoparticles to kill cancer cells. NiZn ferrite nanoparticle suspensions were found to have an average hydrodynamic diameter, polydispersity index, and zeta potential of 254.2 ± 29.8 nm, 0.524 ± 0.013, and −60 ± 14 mV, respectively. We showed that NiZn ferrite nanoparticles had selective toxicity towards MCF-7, HepG2, and HT29 cells, with a lesser effect on normal MCF 10A cells. The quantity of Bcl-2, Bax, p53, and cytochrome C in the cell lines mentioned above was determined by colorimetric methods in order to clarify the mechanism of action of NiZn ferrite nanoparticles in the killing of cancer cells. Our results indicate that NiZn ferrite nanoparticles promote apoptosis in cancer cells via caspase-3 and caspase-9, downregulation of Bcl-2, and upregulation of Bax and p53, with cytochrome C translocation. There was a concomitant collapse of the mitochondrial membrane potential in these cancer cells when treated with NiZn ferrite nanoparticles. This study shows that NiZn ferrite nanoparticles induce glutathione depletion in cancer cells, which results in increased production of reactive oxygen species and eventually, death of cancer cells.
机译:本研究的长期目标是确定NiZn铁氧体纳米颗粒杀死癌细胞的能力。发现NiZn铁氧体纳米颗粒悬浮液的平均流体动力学直径,多分散指数和Zeta电位分别为254.2±29.8 nm,0.524±0.013和-60±14 mV。我们显示,NiZn铁氧体纳米颗粒对MCF-7,HepG2和HT29细胞具有选择性毒性,对正常MCF 10A细胞的影响较小。通过比色法确定上述细胞系中Bcl-2,Bax,p53和细胞色素C的含量,以阐明NiZn铁氧体纳米颗粒在杀死癌细胞中的作用机理。我们的结果表明,NiZn铁氧体纳米颗粒通过caspase-3和caspase-9促进癌细胞的凋亡,Bcl-2的下调以及Bax和p53的上调以及细胞色素C的移位。当用NiZn铁氧体纳米粒子治疗时,这些癌细胞中的线粒体膜电位随之降低。这项研究表明,NiZn铁氧体纳米颗粒可诱导癌细胞中的谷胱甘肽耗竭,从而导致活性氧的产生增加,并最终导致癌细胞死亡。

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