Anticancer Cardenolides from the aerial parts of Calortopis procera

Column chromatography (CC) analysis of methanol and butanol extracts of the aerial parts of well as the methanol extract of its latex, led to the isolation of cardenolides, of which the structures were elucidated by NMR and HRESIMS spectroscopy. They also revealed several triterpenes and flavonoid g...

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Published inZeitschrift für Naturforschung C. A journal of biosciences Vol. 76; no. 5; pp. 243 - 250
Main Authors Sweidan, Nuha, Esawi, Ezaldeen, Ismail, Mohammad, Alshaer, Walhan
Format Journal Article
LanguageEnglish
Published Germany De Gruyter 26.05.2021
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Summary:Column chromatography (CC) analysis of methanol and butanol extracts of the aerial parts of well as the methanol extract of its latex, led to the isolation of cardenolides, of which the structures were elucidated by NMR and HRESIMS spectroscopy. They also revealed several triterpenes and flavonoid glycoside. Based on the antiproliferative activity reported for cardenolides, the activity of calotropin and calotoxin was tested against two common cancer cell lines, human triple-negative breast cancer cell line (MDA-MB-231) and human lung adenocarcinoma cell line (A549). The high toxicity of the latex also encouraged performing the same test on the same cancer cell lines. The anti-proliferative activity of calotropin and calotoxin was compared to the methanol extract and the wax of the latex. The results showed that calotropin and calotoxin have significant cytotoxicity against MDA-MB-231 and A549 cell lines ranging from 0.046 to 0.072 μM compared to the methanol extract and the wax of its latex ranging from 0.47 to 58.41 μM. Moreover, the results showed lower toxicity of all treatments to the human skin fibroblasts compared to the toxicity to both MDA-MB-231 and A549 cancer cells lines except the higher toxicity of Methanolic extracts of latex to the MDA-MB-231 cells. In conclusion, is a medicinal plant with a wide spectrum of cardinolides including calotropin and calotoxin, which are promising agents for targeted cancer phytotherapy.
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ISSN:0939-5075
1865-7125
DOI:10.1515/znc-2020-0281