Browsing by Author "Ghada M. Aleid"

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    Caffeine-boosted silver nanoparticles target breast cancer cells by triggering oxidative stress, inflammation, and apoptotic pathways
    (Elsevier B.V., 2025-05-14) Naief Dahran; Mohamed S. Othman; Farah Mumtaz; Ghada M. Aleid; Mohamed E. Ghoniem; Mai A. Samak; Mohamed T. Elabbasy; Ayman A. Saleh; Sofian T. Obeidat; Ola A. Habotta; Ahmed E. Abdel Moneim
    Breast cancer (BC) constitutes a major global health concern and is the second foremost cause of cancer-related mortality among women worldwide. This research investigated the anticancer effectiveness of caffeine-conjugated silver nanoparticles (Caf-AgNPs) against MDA-MB-231 breast cancer cells, utilizing fluorouracil (5-FU) as a reference antitumor drug. The study illustrated that the strategic conjugation of caffeine with AgNPs substantially improved the therapeutic efficacy against breast cancer cell lines and simultaneously attenuated cytotoxicity in normal mouse liver (NBL) cells. Caf-AgNPs significantly increased ROS, malondialdehyde, COX-2, IL-1β, and TNF-α level in BC cells, which was accompanied by a decrease in glutathione levels. The increased levels of cytosolic cytochrome c, caspase-3, and Bax proteins, as well as a significant decrease in Bcl-2 expression and Bcl-2/Bax ratio, were indicative of the significant pro-apoptotic effects of Caf-AgNPs in MDA-MB-231 cells. Cancer cells subjected to Caf-AgNPs demonstrated elevated lactate dehydrogenase (LDH) membrane leakage, signifying cellular membrane disruption. Cell cycle analysis revealed a substantial proportion of early and late stage apoptosis in cancer cells exposed to Caf-AgNPs, accompanied by a notable downregulation of cyclin D1 and cyclin-dependent kinase 2 (CDK2) mRNA expression. Caf-AgNPs utilize several mechanisms for cellular destruction, including cell cycle arrest, oxidative stress induction, modulation of the inflammatory response, and mitochondrial apoptosis. Caf-AgNPs offer a promising and complex strategy for breast cancer intervention. © 2025 American Pharmacists Association
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    Evaluation of Vincamine Loaded with Silver Nanoparticles as a New Potential Therapeutic Agent Against Ehrlich’s Solid Carcinoma in Mice
    (Multidisciplinary Digital Publishing Institute (MDPI), 2024-11-01) Naief Dahran; Mohamed S. Othman; Mohamed E. Ghoniem; Mai A. Samak; Mohamed T. Elabbasy; Sofian T. Obeidat; Ghada M. Aleid; Shimaa Abo Elnaga; Azza M. Khaled; Aya A. Altaleb; Ahmed E. Abdel Moneim
    Vincamine, a monoterpenoid indole alkaloid with vasodilatory properties, is extracted from the leaves of Vinca minor. The present study aimed to determine the potential anticancer effects of vincamine loaded in silver nanoparticles (VCN-AgNPs) in mice with Ehrlich solid carcinoma (ESC). After tumor transplantation, the mice were divided into five groups: ESC, ESC+Cisplatin (CPN; 5 mg/kg), ESC+VCN (40 mg/kg), ESC+AgNPs (6 mg/kg), and ESC+VCN-AgNPs (20 mg/kg). The administration of VCN-AgNPs to ESC-bearing mice improved their survival rate and reduced their body weight, tumor size, and tumor weight compared to the ESC group. Furthermore, VCN-AgNPs intensified oxidative stress in tumor tissues, as evidenced by elevated levels of lipid peroxidation (LPO) and nitric oxide (NO), along with a reduction in the levels of the antioxidants investigated (GSH, GPx, GR, SOD, CAT, and TAC). Furthermore, VCN-AgNPs increased the apoptotic proteins Bax and caspase-3, decreased the anti-apoptotic protein (Bcl-2), increased the inflammatory markers TNF-α and IL-1β, and inhibited angiogenesis by lowering VEGF levels in tumor tissues, all of which led to apoptosis. Furthermore, histopathological studies showed that VCN-AgNPs suppressed the progression of Ehrlich carcinoma and induced the formation of clusters of necrotic and fragmented tumor cells. VCN-AgNPs possess cytotoxic and genotoxic effects against ESC because of their pro-oxidant, pro-apoptotic, pro-inflammatory, and antiangiogenic effects. Additionally, the combination of VCN-AgNPs was more effective and safer than chemically synthesized AgNPs, as indicated by an increase in the lifespan of animals and the total tumor inhibition index.