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Evaluation of the Anticancer Potential of Crude,Irradiated Cerastes cerastes Snake Venom and Propolis Ethanolic Extract & Related Biological Alterations
Authors:Mostafa I Abdelglil  Sanaa O Abdallah  Mohamed A El-Desouky  Mohammad Y Alfaifi  Serag Eldin I Elbehairi  Aly F Mohamed
Institution:1.Faculty of Sciences, Cairo University, Giza 12613, Egypt;2.Biology Department, Faculty of Science, King Khalid University, Abha 9004, Saudi Arabia;3.Cell Culture Lab, Egyptian Organization for Biological Products and Vaccines (VACSERA Holding Company), 51 Wezaret El-Zeraa St., Agouza, Giza 12654, Egypt;4.The International Center for Training & Advanced Researches (ICTAR–Egypt), Cairo 11647, Egypt;
Abstract:We aimed to evaluate the anticancer potential of crude venom (CV), γ irradiated Certastes cerastes venom (IRRV), and propolis ethanolic extract (PEE). IRRV showed a higher toxicity than CV, while CV-PEE showed higher toxicity than IRRV and CV against lung A549] and prostate PC3] cancer cells. Toxicity to A549] and PC3] cells was concentration and cell type dependent. In comparison to controls, apoptotic genes showed a significant upregulation of P53 and Casp-3 and a downregulation of Bcl-2. Also, induced elevated DNA accumulation in the S] phase post PC3 cell treatment with IRRV and CV, as well as a significant DNA accumulation at G2/M phase after IRRV treatment of A549 cells. In contrast, PC3 cells showed a negligible cellular DNA accumulation after PEE treatment. Glutathione reductase GR] was reduced in case of PC3 and A549 cell treated with IRRV, CV, and PEE compared with its values in untreated cell control. The Malondialdehyde MDA] values in both cells recorded a significant elevation post IRRV treatment compared to the rest of the treatment regimen and untreated cell control. Similarly, IRRV and CV-PEE mix showed obviously higher reactive oxygen species ROS] values than PC3 and A549 cell treatments with CV and PEE.
Keywords:PEE  IRR V  A549  PC3  apoptotic  IC50  CV  P53  Casp-3  Bcl-2  ROS  MDA  and GR
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