Phyto-mediated synthesis of CuO nanoparticles using aqueous leaf extract of Artemisia deserti and their anticancer effects on A2780-CP cisplatin-resistant ovarian cancer cells

被引:0
作者
Sepideh Shahriary
Farzaneh Tafvizi
Parvin Khodarahmi
Masoud Shaabanzadeh
机构
[1] Islamic Azad University,Department of Biology, Parand Branch
[2] Islamic Azad University,Department of Chemistry, Damghan Branch
来源
Biomass Conversion and Biorefinery | 2024年 / 14卷
关键词
Apoptosis; CuO nanoparticles; Cisplatin resistant; Green synthesis; Ovarian cancer;
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学科分类号
摘要
Cancer is the second leading cause of death in the word. The failure of the most common therapeutic strategies including chemotherapy and its side effects on normal tissues plus the development of chemoresistance cases has justified the global attempt to find an alternative medicinal approach for cancer treatment. The purpose of this study was to analyze the effect of green-synthesized CuO nanoparticles (CuO NPs) using aqueous leaf extract of the plant Artemisia deserti on A2780-CP cisplatin-resistant ovarian cancer cells. GC–MS analysis of A. deserti extract showed the presence of three main reductive phytocomponents. The properties of synthesized CuO NPs have been characterized using different techniques such as UV–vis, FESEM, TEM, EDX, FTIR, XRD, and DLS. The cytotoxicity effect of CuO NPs has been evaluated by MTT assay. The induction of apoptosis and the cell cycle arrest has been analyzed by flow cytometry and qRT-PCR, respectively. The overall results obtained from MTT assay, Annexin/PI staining, qRT-PCR, cell cycle analysis, and measurement of generated cellular ROS in A2780-CP cells showed that the synthesized CuO NPs could induce apoptosis in A2780-CP cells in a significant level. The results also indicated that the biosynthesized CuO NPs cause negligible amount of cell cytotoxicity on normal healthy human foreskin fibroblasts cells (HFF). These two advantages can make the biogenic synthesized CuO NPs a good candidate for further studies on cancer treatment approaches.
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页码:2263 / 2279
页数:16
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共 199 条
[1]  
Yang J(2018)STAT3-mediated Twist1 upregulation contributes to epithelial-mesenehymal transition in cisplatin resistant ovarian cancer Int J Clin Exp Med 7 6749-6757
[2]  
Sorrentino A(2008)Role of microRNAs in drug-resistant ovarian cancer cells Gynecol Oncol 111 478-486
[3]  
Pokhriyal R(2019)Chemotherapy resistance in advanced ovarian cancer patients Biomark Cancer 11 1-19
[4]  
Shen D-W(2012)Cisplatin resistance: a cellular self-defense mechanism resulting from multiple epigenetic and genetic changes Pharmal Rev 6 706-721
[5]  
de Luca A(2019)A structure-based mechanism of cisplatin resistance mediated by glutathione transferase P1–1 PNAS 116 1-9
[6]  
Parker LJ(2001)Mechanisms of resistance to cisplatin Mutat Res Fundam Molec Mech Mutagen. 478 23-43
[7]  
Kartalu M(2015)Green tea polyphenol EGCG reverse cisplatin resistance of A549/DDP Biomed Pharmacother 69 285-290
[8]  
Essigmann JM(2019)Platinum resistance in ovarian cancer: role of DNA repair Cancers 11 1-15
[9]  
Zhang Y(2010)Enhancing tumor-specific uptake of the anticancer drug cisplatin with a copper chelator Cancer Cell 17 574-583
[10]  
Damia GBM(2017)Changes in the expression of various transporters as influencing factors of resistance to cisplatin Anticancer Res 37 5477-5484