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Induce Apoptosis and Cell Cycle Arrest and Inhibit Metastasis on MCF7 Breast Cancer Cells. | LitMetric

AI Article Synopsis

  • Breast cancer is a leading cause of cancer-related deaths in women, highlighting the need for new treatment options, particularly from plant sources.
  • A study tested the antioxidant properties and effects of extracts from three Nigerian medicinal plants on MCF7 breast cancer cells, finding significant inhibitory effects and the highest potency in specific extracts.
  • Analysis revealed that these effective extracts contain various beneficial compounds, suggesting their potential as sources for developing new anticancer treatments.

Article Abstract

Despite the availability of anticancer drugs, breast cancer remains the most death-causing tumor-related disease in women. Hence, there is a need for discovery and development of efficient alternative drugs, and sources such as plants need to be explored. In this study, antioxidant capacities and inhibitory effects against MCF7 cells of the extracts of stem bark of three Nigerian medicinal plants (, and ) were investigated. The extracts had the highest antioxidant and antiproliferative effects, followed by that of , and the extracts had minimal effects. The IC values of the methanol and aqueous extracts from the three plants that inhibited the proliferation of MCF7 cells ranged from 78-> 500 g/ml. Moreover, all the plant extracts but the aqueous extract of exhibited antimetastatic action and induced apoptosis and cell cycle arrest in MCF7 cells. Liquid chromatography/time-of-flight/mass spectrometry profiling revealed that the five potent extracts contain many phenols and omega-6 fatty acids, and some of the identified compounds (isorhamnetin, eupatorin, alpinumisoflavone, procyanidin B3, syringin, and gallic acid) have been reported to have antiproliferative effects on cancer cells. Hence, the stem bark of these plants could be potential sources of antibreast cancer agents.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556270PMC
http://dx.doi.org/10.1155/2019/6104574DOI Listing

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