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:25
作者
Shahriary, Sepideh [1 ]
Tafvizi, Farzaneh [1 ]
Khodarahmi, Parvin [1 ]
Shaabanzadeh, Masoud [2 ]
机构
[1] Islamic Azad Univ, Dept Biol, Parand Branch, Parand, Iran
[2] Islamic Azad Univ, Dept Chem, Damghan Branch, Damghan, Iran
关键词
Apoptosis; Artemisia deserti; CuO nanoparticles; Cisplatin resistant; Green synthesis; Ovarian cancer; COPPER-OXIDE NANOPARTICLES; ANTIBACTERIAL ACTIVITY; SILVER NANOPARTICLES; APOPTOSIS INDUCTION; GREEN SYNTHESIS; CYTOTOXICITY; MEDICINE; PLANT; SENSITIZATION; BIOSYNTHESIS;
D O I
10.1007/s13399-022-02436-x
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
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.
引用
收藏
页码:2263 / 2279
页数:17
相关论文
共 100 条
[1]   Sesquiterpenes and their derivatives-natural anticancer compounds: An update [J].
Abu-Izneid, Tareq ;
Rauf, Abdur ;
Shariati, Mohammad Ali ;
Khalil, Anees Ahmed ;
Imran, Muhammad ;
Rebezov, Maksim ;
Uddin, Md Sahab ;
Mahomoodally, Mohamad Fawzi ;
Rengasamy, Kannan R. R. .
PHARMACOLOGICAL RESEARCH, 2020, 161
[2]   Kinetic aspects of platinum anticancer agents [J].
Ahmad, Saeed .
POLYHEDRON, 2017, 138 :109-124
[3]   Synergistic anticancer activity of dietary tea polyphenols and bleomycin hydrochloride in human cervical cancer cell: Caspase-dependent and independent apoptotic pathways [J].
Alshatwi, Ali A. ;
Periasamy, Vaiyapuri Subbarayan ;
Athinarayanan, Jegan ;
Elango, Ramesh .
CHEMICO-BIOLOGICAL INTERACTIONS, 2016, 247 :1-10
[4]   Copper oxide nanoparticles-loaded zeolite and its characteristics and antibacterial activities [J].
Alswat, Abdullah A. ;
Bin Ahmad, Mansor ;
Hussein, Mohd Zobir ;
Ibrahim, Nor Azowa ;
Saleh, Tawfik A. .
JOURNAL OF MATERIALS SCIENCE & TECHNOLOGY, 2017, 33 (08) :889-896
[5]   Cisplatin resistance and opportunities for precision medicine [J].
Amable, Lauren .
PHARMACOLOGICAL RESEARCH, 2016, 106 :27-36
[6]  
Aslanturk O.S., 2018, GENOTOXICITY PREDICT, P1, DOI [DOI 10.5772/INTECHOPEN.71923, 10.5772/intechopen.71923]
[7]   Characterization and evaluation of cytotoxic and apoptotic effects of green synthesis of silver nanoparticles using Artemisia Ciniformis on human gastric adenocarcinoma [J].
Aslany, Shahrzad ;
Tafvizi, Farzaneh ;
Naseh, Vahid .
MATERIALS TODAY COMMUNICATIONS, 2020, 24
[8]   Correlation of adverse effects of cisplatin administration in patients affected by solid tumours: A retrospective evaluation [J].
Astolfi, Laura ;
Ghiselli, Sara ;
Guaran, Valeria ;
Chicca, Milvia ;
Simoni, Edi ;
Olivetto, Elena ;
Lelli, Giorgio ;
Martini, Alessandro .
ONCOLOGY REPORTS, 2013, 29 (04) :1285-1292
[9]  
Azizi M, 2017, PLOS ONE, V12, DOI [10.1371/Journal.pone.0188639, 10.1371/journal.pone.0188639]
[10]  
Beale PJ, 2000, BRIT J CANCER, V82, P436