
doi: 10.1111/bcpt.13664
pmid: 34605186
AbstractPlants of the Calea genus have been reported to contain lipophilic compounds, such as sesquiterpene lactones, with cytotoxic effect against different cancer cell lines. The aim of this manuscript was to investigate the chemical profile and cytotoxic activity of different fractions from Calea phylolepis leaves on different human cancer cell lines. The fractions were prepared using solvent extraction of increasing polarity, yielding hexane, ethyl acetate and methanolic fractions. All fractions were chemically analysed by thin layer chromatography (TLC), and their cytotoxic activity against HT‐29 (colon adenocarcinoma), MCF‐7 (breast cancer), U‐251MG (malignant glioblastoma) and L929 (mouse fibroblast) cell lines was investigated. Among these, the hexane and ethyl acetate fractions showed higher cytotoxic effects, while the methanolic fraction did not show any cytotoxic effects. The major bioactive compound from the hexane fraction (12.15%) was isolated using chromatographic methods and was identified by nuclear magnetic resonance spectroscopy (NMR) and gas chromatography–mass spectrometry (GC–MS) analysis as 6‐epi‐β‐verbesinol coumarate. This compound showed activity against breast cancer cells (IC50 = 5.8 ± 1.0 μg/ml), similar to etoposide. Furthermore, 6‐epi‐β‐verbesinol coumarate showed low cytotoxicity to normal fibroblast cells, suggesting a high selectivity index (SI = 7.39) against breast cancer cells.
Magnetic Resonance Spectroscopy, Plant Extracts, Breast Neoplasms, Asteraceae, Fibroblasts, Antineoplastic Agents, Phytogenic, Gas Chromatography-Mass Spectrometry, Cell Line, Plant Leaves, Inhibitory Concentration 50, Mice, Cell Line, Tumor, Neoplasms, MCF-7 Cells, Animals, Humans, Female, HT29 Cells
Magnetic Resonance Spectroscopy, Plant Extracts, Breast Neoplasms, Asteraceae, Fibroblasts, Antineoplastic Agents, Phytogenic, Gas Chromatography-Mass Spectrometry, Cell Line, Plant Leaves, Inhibitory Concentration 50, Mice, Cell Line, Tumor, Neoplasms, MCF-7 Cells, Animals, Humans, Female, HT29 Cells
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