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Systematic Review of Potential Anticancerous Activities of

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Journal Plants (Basel)
Date 2022 Jan 11
PMID 35009024
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Abstract

The objective of this study was to carry out a systematic review of the substances isolated from the African medicinal plant focusing on compounds harboring activities against cancer models detailed in depth herein at both in vitro and in vivo preclinical levels. The review was conducted through Pubmed and Google Scholar. Nineteen out of the forty-two secondary metabolites isolated to date from displayed interesting in vitro and/or in vivo antitumor activities. They belonged to alkaloid (Erysodine), triterpenes (Erythrodiol, maniladiol, oleanolic acid), prenylated isoflavonoids (senegalensin, erysenegalensein E, erysenegalensein M, alpinumisoflavone, derrone, warangalone), flavonoids (erythrisenegalone, senegalensein, lupinifolin, carpachromene) and pterocarpans (erybraedine A, erybraedine C, phaseollin). Among the isoflavonoids called "erysenegalensein", only erysenealenseins E and M have been tested for their anticancerous properties and turned out to be cytotoxic. Although the stem bark is the most frequently used part of the plant, all pterocarpans were isolated from roots and all alkaloids from seeds. The mechanisms of action of its metabolites include apoptosis, pyroptosis, autophagy and mitophagy via the modulation of cytoplasmic proteins, miRNA and enzymes involved in critical pathways deregulated in cancer. Alpinumisoflavone and oleanolic acid were studied in a broad spectrum of cancer models both in vitro and in preclinical models in vivo with promising results. Other metabolites, including carpachromen, phaseollin, erybraedin A, erysenegalensein M and maniladiol need to be further investigated, as they display potent in vitro effects.

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References
1.
Li L, Wei L, Shen A, Chu J, Lin J, Peng J . Oleanolic acid modulates multiple intracellular targets to inhibit colorectal cancer growth. Int J Oncol. 2015; 47(6):2247-54. DOI: 10.3892/ijo.2015.3198. View

2.
Wu H, Zhong Q, Zhong R, Huang H, Xia Z, Ke Z . Preparation and antitumor evaluation of self-assembling oleanolic acid-loaded Pluronic P105/d-α-tocopheryl polyethylene glycol succinate mixed micelles for non-small-cell lung cancer treatment. Int J Nanomedicine. 2016; 11:6337-6352. PMC: 5135287. DOI: 10.2147/IJN.S119839. View

3.
Shukla R, Urandur S, Banala V, Marwaha D, Gautam S, Rai N . Development of putrescine anchored nano-crystalsomes bearing doxorubicin and oleanolic acid: deciphering their role in inhibiting metastatic breast cancer. Biomater Sci. 2021; 9(5):1779-1794. DOI: 10.1039/d0bm01033b. View

4.
Wang F, Hua H, Pei Y, Chen D, Jing Y . Triterpenoids from the resin of Styrax tonkinensis and their antiproliferative and differentiation effects in human leukemia HL-60 cells. J Nat Prod. 2006; 69(5):807-10. DOI: 10.1021/np050371z. View

5.
Gao Y, Yuan Y, Song G, Lin S . Inhibitory effect of ursolic acid and oleanolic acid from Eriobotrya fragrans on A549 cell viability in vivo. Genet Mol Res. 2016; 15(2). DOI: 10.4238/gmr.15028642. View