Background: Red onion (Allium cepa L.) peels represent an abundant agricultural byproduct rich in bioactive flavonoids, yet their therapeutic potential against aggressive breast cancer models remains poorly characterized. This study aimed to extract and purify anthocyanins from red onion peels, characterize their active constituents, and evaluate their selective in vitro cytotoxicity against the triple-negative breast cancer (TNBC) cell line CAL-51 relative to non-tumorigenic Normal Human Fibroblast (NHF) cells. Methods: Anthocyanins were extracted with acidified aqueous ethanol, purified using silica gel G60 column chromatography and characterized by reversed-phase high-performance liquid chromatography (RP-HPLC). Cytotoxicity was evaluated through 72-hour MTT assays on CAL-51 and NHF cells, confirmed by phase-contrast morphological analysis and analyzed using one-way ANOVA. Results: Through RP-HPLC, malvidin and peonidin were characterized as the major monomeric anthocyanidins. According to the results, the purified extract demonstrated a potent and cell line-dependent dose effect for the cytotoxicity of CAL-51 cells with IC50 = 247.5 μg/mL (maximum inhibition: 63.73% at 1000 µg/mL), accompanied by morphological hallmarks of apoptosis. In contrast, the extract exhibited much lower toxicity against NHF cells (IC50=1767 µg/mL; maximum inhibition: 17.39% at 10,000 µg/mL), resulting in a good selectivity index of 7.1. Conclusion: Purified red onion peel anthocyanins were powerful, selective anti-proliferative and pro-apoptotic agents against TNBC in vitro without harming normal cells. This sets a path to exploiting agricultural waste as a source of potential natural therapeutic agents for the individualised treatment of breast cancer in an economically viable manner.
In this manuscript, the effect of substituting strontium with barium on the structural properties of Tl0.8Ni0.2Sr2-xBrxCa2Cu3O9-δcompound with x= 0, 0.2, 0.4, have been studied. Samples were prepared using solid state reaction technique, suitable oxides alternatives of Pb2O3, CaO, BaO and CuO with 99.99% purity as raw materials and then mixed. They were prepared in the form of discs with a diameter of 1.5 cm and a thickness of (0.2-0.3) cm under pressures 7 tons / cm2, and the samples were sintered at a constant temperature o
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Abstract Background: The human epidermal growth factor receptor 2(HER2) proto-oncogene is overexpressed or amplified in approximately 15%-25% of invasive breast cancers. Approximately 35% of HER2-amplified breast cancers have coamplification of the topoisomerase II-alpha (TOP2A) gene encoding an enzyme that is a major target of anthracyclines. Hence, the determination of genetic alteration (amplification or deletion) of both genes is considered as an important predictive factor that determines the response of breast cancer patients to treatment. The aims of this study are to determinate TOP2A status gene amplification in a set of Iraqi patients with breast cancer that have had an equivocal (2+) and positive HER2/neu by immunohistochemistry
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