Synergistic effect of quercetin and cobalt ferrite-graphene oxide-based hyperthermia to inhibit expression of heat shock proteins and induce apoptosis in breast cancer cells

Q4 Pharmacology, Toxicology and Pharmaceutics
F. Mobaraki, H. Nazari, Seyed Ali Lajevardiyan, Shadie Hatamie, H. Jafary, S. Hosseinzadeh
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引用次数: 0

Abstract

Background: Combinatorial medicine includes promising therapeutic methods for diseases such as cancer, whereby various biochemical and physical agents are simultaneously used to remove tumors. For example, the effectiveness of hyperthermia as a new technique for cancer therapy, can be enhanced, if it is combined with chemical compounds. Herein, the influence of quercetin as a heat shock protein (HSP) inhibitor on the efficiency of cobalt ferrite-graphene oxide (CoFe2O4-GO) nanoparticles- based hyperthermia was investigated in an in vitro study. Methods: Firstly, the surface of graphene sheets was decorated with CoFe2O4 nanoparticles (5-8 nm) and assayed using transmission electron microscopy (TEM), vibrating-sample magnetometer (VSM) and X-ray diffraction (XRD) methods. The cytotoxic effect of the corresponding co-implementation was then examined in MCF7 cell line with or without hyperthermia by (3-(4,5-dimethyl thiazolyl-2)-2,5-diphenyltetrazolium bromide) (MTT) test for 24, 48 and 72 hrs. In addition, the expression of Bax, Bcl2 and HSP70 genes and the production of radicals were evaluated by Real-Time PCR and DPPH (2,2-diphenyl-1-picrylhydrazyl) assays respectively. Results: The study showed that the doses associated with the IC50 points for quercetin and the CoFe2O4-GO nanocomposite were 0.02 mg/ml and 0.001 g/ml, respectively. The results showed that the simultaneous treatment of the cancer cells with quercetin, the nanocomposite, and hyperthermia significantly improves the cytotoxicity effect, increases the expression of Bax gene and down-regulates HSP70 and Bcl2 genes. In addition, the greatest attenuation of DPPH free radicals was observed in the corresponding group. Conclusion: The hybrid treatment of quercetin and the nanoparticle in the presence of hyperthermia could be considered as a promising approach for cancer therapy with minor side effects.
槲皮素和铁酸钴-氧化石墨烯热疗抑制乳腺癌细胞热休克蛋白表达和诱导细胞凋亡的协同作用
背景:组合医学包括对癌症等疾病的有前景的治疗方法,即同时使用各种生化和物理药物来切除肿瘤。例如,热疗作为一种治疗癌症的新技术,如果与化合物结合使用,可以提高其有效性。本文在体外研究了槲皮素作为热休克蛋白(HSP)抑制剂对基于铁酸钴-氧化石墨烯(cofe2o4 -氧化石墨烯)纳米颗粒的热疗效率的影响。方法:首先用CoFe2O4纳米颗粒(5 ~ 8 nm)修饰石墨烯片表面,采用透射电镜(TEM)、振动样品磁强计(VSM)和x射线衍射(XRD)等方法对其进行分析。然后通过(3-(4,5-二甲基噻唑-2)-2,5-二苯基溴化四氮唑)(MTT)试验,在24、48和72小时的MCF7细胞株中检测相应的共实施对细胞的毒性作用。此外,采用Real-Time PCR和DPPH (2,2-diphenyl-1-picrylhydrazyl)测定Bax、Bcl2和HSP70基因的表达和自由基的产生。结果:槲皮素和CoFe2O4-GO纳米复合材料的IC50点相关剂量分别为0.02 mg/ml和0.001 g/ml。结果表明,槲皮素、纳米复合材料和热疗同时处理癌细胞可显著提高细胞毒作用,增加Bax基因表达,下调HSP70和Bcl2基因表达。此外,DPPH自由基在相应组的衰减最大。结论:槲皮素与纳米粒子在高温条件下联合应用是一种治疗肿瘤的有效方法,副作用小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.10
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0.00%
发文量
17
审稿时长
10 weeks
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