Cactus and lupin extracts as prospective anticancer agents compared with utoral drug.

J Food Biochem

The Holding Company for the Production of Vaccines, Sera and Drugs (VACSERA-Egy Vac), Giza, Egypt.

Published: August 2020

AI Article Synopsis

  • The study examined the anticancer effects of ethanolic extracts from cactus and lupin on colon cancer cells, specifically focusing on their antioxidant and cytotoxic properties.
  • Lupin extract showed the highest levels of bioactive compounds and significant cytotoxic effects, particularly in regulating genes related to apoptosis.
  • Overall, both lupin and cactus extracts demonstrate strong potential as natural anticancer agents, with lupin extract being the most effective for therapeutic applications.

Article Abstract

The ethanolic extracts of many plants have been used in alternative medicine. The present study aimed at evaluating the antioxidant, cytotoxicity, and anticancer potential of cactus and lupin ethanolic extracts compared to utoral drug (UT) on the colon Caco-2 cancer cell line. Bioactive components, cytotoxicity of Caco-2 cell cycle, and gene regulation of apoptosis genes were studied by HPLC, flow cytometer, and RT-PCR, respectively. Lupin extract (LE) contained high bioactive components and antioxidant potential. The predominant phenol, flavonoid, and sterol in LE were rosmarinic acid (2,004.8 μg/ml), quercetin (9,912 µg/g), and ergosterol (2.77 µg/g). LE and its mixture with utoral showed high cytotoxicity and effective potential in regulation of gene expression of proapoptotic and antiapoptotic genes in Caco-2 cells. In conclusion, LE and cactus extract (CE) could be considered as natural preparations with high anticancer properties against Caco-2 cells. LE had the highest anticancer potential among the tested preparations. PRACTICAL APPLICATIONS: The study demonstrated that lupine and cactus extracts have high potential as anticancer substances. These natural extracts can be used to prepare therapeutic mixtures or foods.

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Source
http://dx.doi.org/10.1111/jfbc.13299DOI Listing

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