Abstract

Abstract Antitumor drugs used today have shown significant efficacy and are derived from natural products such as plants. Iso-mukaadial acetate has previously been shown to possess anticancer properties by inducing apoptosis. The purpose of this study was to investigate the therapeutic effect of Iso-mukaadial acetate in the breast cancer xenograft mice model. Female athymic mice were used and were inoculated with breast cancer cells subcutaneously after culturing. Group one served as a negative control group (no treatments) and group two positive control group (cisplatin) which was administered intravenously. Iso-mukaadial acetate treatment was administered orally to group three(100 mg/kg) and group four (500 mg/kg). Blood was collected (70 µL) from the tail vein on day zero, day seven and day 14. Tumor regression was measured, and a pharmacokinetic study was conducted. Estimation of Serum Parameters for Hepatic and Renal Indices were examined using an Automated Chemistry Analyzer. Histopathological analysis was conducted to evaluate morphological changes before and after treatment under a light microscope. Tumor shrinkage was observed after treatment. In conclusion, Iso-mukaadial acetate inhibited tumor progression in breast cancer athymic mice without major side effects. Citation Format: Portia Raphela-Choma, Lesetja R. Motadi, Mpho S. Choene. Antitumor effect of Iso-mukaadial acetate in MCF-7 human cancer xenograft models [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2023; Part 1 (Regular and Invited Abstracts); 2023 Apr 14-19; Orlando, FL. Philadelphia (PA): AACR; Cancer Res 2023;83(7_Suppl):Abstract nr 6126.

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