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Prof. Hussein Abd Elmaksoud Ali :: Publications:

Title:
Molecular study on the potential therapeutic effect of novel nanocompsite on cancerous tumor bearing mice
Authors: Omayma A.R. Abou Zaid, Hussein AbdEl Maksoud, Abdel Fatah M. Badwi, Mohamed A. Hussien and Mohammed F. EL-Shiekha
Year: 2015
Keywords: Curcumin nanoparticles, Zinc Oxide nanoparticles, P53- gene expression
Journal: BENHA VETERINARY MEDICAL JOURNAL
Volume: 28
Issue: 1
Pages: 98‐108
Publisher: BENHA VETERINARY MEDICAL JOURNAL
Local/International: International
Paper Link:
Full paper Not Available
Supplementary materials Not Available
Abstract:

Nanoparticles are making significant contributions to the development of new approaches of drug delivery in cancer and can provide a platform for combined therapeutics with subsequent monitoring of response. Basic curcumin and zinc oxide (ZnO) nanocompsite modified with vitamin C and CTAB have been exert chemopreventative activity against cancer in mice animal model. This study was carried out on 80 mice and were divided into four groups, each groups have (20 mice) Group 1: NTBM (Negative control) .Group 2: TBM- (Positive control). Group 3: NTBM-treated with nanocompsite orally (1.850 g/kg /day) for 6 weeks. Group 4: TBM-treated with nanocompsite orally (1.850 g/kg /day) for 6 weeks. Liver tissues sample were collected from all mice by decapitation after 2, 4 and 6 weeks from the onset of treatment, then obtained in dry and clean tubes then kept in a deep freeze at -20 and processed, total RNA isolation and quantitative real time PCR analysis for apoptotic marker (P53- gene expression), apoptotic DNA ladder assay and estimation of protein. We observed that nanocompsite have distinct effects on liver cell viability via killing cancer cells, while posing no effect on normal cells (hepatocytes). The marked difference in cytotoxicity between cancer cells and normal cells suggests an exciting potential for nanocompsite as novel alternatives to cancer therapy. Our molecular data showed that both mRNA and protein levels of tumor suppressor gene p53 were upregulated and induce activity of DNA fragmentation in liver cells.

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