...
首页> 外文期刊>International Journal of Nanomedicine >Novel biomolecule lycopene-reduced graphene oxide-silver nanoparticle enhances apoptotic potential of trichostatin A in human ovarian cancer cells (SKOV3)
【24h】

Novel biomolecule lycopene-reduced graphene oxide-silver nanoparticle enhances apoptotic potential of trichostatin A in human ovarian cancer cells (SKOV3)

机译:新型生物分子番茄红素还原的氧化石墨烯-银纳米颗粒可增强曲古抑菌素A在人卵巢癌细胞(SKOV3)中的凋亡潜能

获取原文
           

摘要

Background: Recently, there has been much interest in the field of nanomedicine to improve prevention, diagnosis, and treatment. Combination therapy seems to be most effective when two different molecules that work by different mechanisms are combined at low dose, thereby decreasing the possibility of drug resistance and occurrence of unbearable side effects. Based on this consideration, the study was designed to investigate the combination effect of reduced graphene oxide-silver nanoparticles (rGO-AgNPs) and trichostatin A (TSA) in human ovarian cancer cells (SKOV3). Methods: The rGO-AgNPs were synthesized using a biomolecule called lycopene, and the resultant product was characterized by various analytical techniques. The combination effect of rGO-Ag and TSA was investigated in SKOV3 cells using various cellular assays such as cell viability, cytotoxicity, and immunofluorescence analysis. Results: AgNPs were uniformly distributed on the surface of graphene sheet with an average size between 10 and 50 nm. rGO-Ag and TSA were found to inhibit cell viability in a dose-dependent manner. The combination of rGO-Ag and TSA at low concentration showed a significant effect on cell viability, and increased cytotoxicity by increasing the level of malondialdehyde and decreasing the level of glutathione, and also causing mitochondrial dysfunction. Furthermore, the combination of rGO-Ag and TSA had a more pronounced effect on DNA fragmentation and double-strand breaks, and eventually induced apoptosis. Conclusion: This study is the first to report that the combination of rGO-Ag and TSA can cause potential cytotoxicity and also induce significantly greater cell death compared to either rGO-Ag alone or TSA alone in SKOV3 cells by various mechanisms including reactive oxygen species generation, mitochondrial dysfunction, and DNA damage. Therefore, this combination chemotherapy could be possibly used in advanced cancers that are not suitable for radiation therapy or surgical treatment and facilitate overcoming tumor resistance and disease progression.
机译:背景:最近,在纳米医学领域已经引起了很多兴趣,以改善预防,诊断和治疗。当通过不同机制起作用的两个不同分子以低剂量组合时,联合疗法似乎是最有效的,从而降低了耐药性和产生难以忍受的副作用的可能性。基于此考虑,本研究旨在研究还原型氧化石墨烯-银纳米颗粒(rGO-AgNPs)和曲古抑菌素A(TSA)在人卵巢癌细胞(SKOV3)中的联合作用。方法:使用称为番茄红素的生物分子合成rGO-AgNPs,并通过各种分析技术对所得产物进行表征。使用各种细胞测定法(例如细胞活力,细胞毒性和免疫荧光分析)研究了SKOV3细胞中rGO-Ag和TSA的联合作用。结果:AgNPs均匀地分布在石墨烯片的表面上,平均尺寸在10到50nm之间。发现rGO-Ag和TSA以剂量依赖性方式抑制细胞活力。低浓度的rGO-Ag和TSA的组合对细胞活力有显着影响,并通过增加丙二醛水平和降低谷胱甘肽水平来增加细胞毒性,还引起线粒体功能障碍。此外,rGO-Ag和TSA的组合对DNA片段化和双链断裂具有更明显的影响,并最终诱导了细胞凋亡。结论:这项研究是第一个报告rGO-Ag和TSA的组合可引起潜在的细胞毒性,并且与SKOV3细胞中单独的rGO-Ag或单独的TSA相比,可通过各种机制(包括活性氧生成)引起更大的细胞死亡,线粒体功能障碍和DNA损伤。因此,这种联合化疗可能被用于不适合放疗或手术治疗的晚期癌症,并有助于克服肿瘤的抵抗力和疾病进展。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号