Crude Flavonoid Extract of the Medicinal Herb Nigella sativa Inhibits Proliferation and Induces Apoptosis in Breast Cancer Cells
Breast cancer is a major cause of morbidity in women worldwide, thus necessitating the identification of novel therapeutic options. The present study aimed to investigate the inhibitory effects of a crude flavonoid extract (CFENS) isolated from the medicinal herb Nigella sativa on the proliferation of MCF-7 human breast cancer cells and to elucidate the mechanism of action. The MCF-7 cell viability was examined by an MTT assay. Fluorescent microscopy, flow cytometry analyses, and agarose gel electrophoresis were carried out to assess the pro-apoptotic potentiality of CFENS. Western blot analyses were done to detect gene expression. The findings showed that CFENS dose-dependently inhibited proliferation and induced apoptosis in MCF-7 cells. Typical morphologic and biochemical changes of apoptosis, including cell shrinkage and detachment, nuclear condensation, and DNA damage, were observed after the CFENS treatments. CFENS triggered ROS accumulation, GSH depletion, disruption of mitochondrial membrane potential, activation of caspases-3/7 and -9, and an increase in the Bax/Bcl-2 ratio in MCF-7 cells. In addition, CFENS induced cell cycle arrest, upregulated the expression levels of p53 and p21 proteins, and downregulated the expression of cyclin D1. These findings indicate that CFENS may help prevent breast cancer and may potentially be a useful agent for the treatment of certain malignancies.
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Document Type: Research Article
Publication date: December 1, 2017
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- Journal of Biomaterials and Tissue Engineering (JBT) is an international peer-reviewed journal that covers all aspects of biomaterials, tissue engineering and regenerative medicine. The journal focuses on the broad spectrum of research topics including all types of biomaterials, their properties, bioimplants and medical devices, biofilms, bioimaging, BioMEMS/NEMS, biosensors, fibers, tissue scaffolds, tissue engineering and modeling, artificial organs, tissue interfaces, interactions between biomaterials, blood, cells, tissues, and organs, regenerative medicine and clinical performance.
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