AI Article Synopsis

  • Medicinal plant-based therapies, like Ricinus communis L. (castor plant) fruit extract (RCFE), show promise for cancer treatment due to their effectiveness, affordability, and minimal side effects.
  • RCFE exhibits strong anti-cancer properties, inducing cytotoxicity and apoptosis in breast cancer cells (MCF-7 and MDA-MB-231) while inhibiting their metastasis and reducing tumor volume in mice.
  • Analysis reveals four active compounds in RCFE that contribute to its anti-cancer effects, suggesting its potential as a viable treatment option for breast cancer.

Article Abstract

Medicinal plant-based therapies can be important for treatment of cancer owing to high efficiency, low cost and minimal side effects. Here, we report the anti-cancer efficacy of Ricinus communis L. fruit extract (RCFE) using estrogen positive MCF-7 and highly aggressive, triple negative MDA-MB-231 breast cancer cells. RCFE induced cytotoxicity in these cells in dose and time-dependent manner. It also demonstrated robust anti-metastatic activity as it significantly inhibited migration, adhesion, invasion and expression of matrix metalloproteinases (MMPs) 2 and 9 in both cell lines. Further, flow cytometry analysis suggested RCFE-mediated induction of apoptosis in these cells. This was supported by attenuation of anti-apoptotic Bcl-2, induction of pro-apoptotic Bax and caspase-7 expressions as well as PARP cleavage upon RCFE treatment. RCFE (0.5 mg/Kg body weight) treatment led to significant reduction in tumor volume in 4T1 syngeneic mouse model. HPLC and ESI-MS analysis of active ethyl acetate fraction of RCFE detected four compounds, Ricinine, p-Coumaric acid, Epigallocatechin and Ricinoleic acid. Individually these compounds showed cytotoxic and migration-inhibitory activities. Overall, this study for the first time demonstrates the anti-cancer efficacy of the fruit extract of common castor plant which can be proposed as a potent candidate for the treatment of breast cancer.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6787038PMC
http://dx.doi.org/10.1038/s41598-019-50769-xDOI Listing

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