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image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Basic & Clinical Pha...arrow_drop_down
image/svg+xml Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao Closed Access logo, derived from PLoS Open Access logo. This version with transparent background. http://commons.wikimedia.org/wiki/File:Closed_Access_logo_transparent.svg Jakob Voss, based on art designer at PLoS, modified by Wikipedia users Nina and Beao
Basic & Clinical Pharmacology & Toxicology
Article . 2021 . Peer-reviewed
License: Wiley Online Library User Agreement
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Bioguided isolation of a selective compound from Calea phyllolepis leaves against breast cancer cells

Authors: Rodrigo Bitencourt Da Rosa; Guilherme Borsoi; Lucas Umpierre Conter; Cleverson Feistel; Anderson Leonardo Gottems; Flávio Henrique Reginatto; Ivana Grivicich; +1 Authors

Bioguided isolation of a selective compound from Calea phyllolepis leaves against breast cancer cells

Abstract

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.

Keywords

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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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
1
Average
Average
Average
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Cancer Research
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