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Feature-Based Molecular Networking for the Exploration of the Metabolome Diversity of Common Egyptian Centaurea Species in Relation to Their Cytotoxic Activity

Authors :
Eman H. Reda
Nesrine M. Hegazi
Mona Marzouk
Zienab T. Abdel Shakour
Ali M. El-Halawany
El-Sayeda A. El-Kashoury
Tarik A. Mohamed
Mahmoud A. A. Ibrahim
Khaled A. Shams
Nahla S. Abdel-Azim
Christopher J. Kampf
Thomas Efferth
Paul. W. Paré
Mohamed-Elamir F. Hegazy
Source :
Molecules, Vol 28, Iss 2, p 674 (2023)
Publication Year :
2023
Publisher :
MDPI AG, 2023.

Abstract

Centaurea is a genus compromising over 250 herbaceous flowering species and is used traditionally to treat several ailments. Among the Egyptian Centaurea species, C. lipii was reported to be cytotoxic against multidrug-resistant cancer cells. In this context, we aimed to explore the metabolome of C. lipii and compare it to other members of the genus in pursuance of identifying its bioactive principles. An LC-MS/MS analysis approach synchronized with feature-based molecular networks was adopted to offer a holistic overview of the metabolome diversity of the Egyptian Centaurea species. The studied plants included C. alexandrina, C. calcitrapa, C. eryngioides, C. glomerata, C. lipii, C. pallescens, C. pumilio, and C. scoparia. Their constitutive metabolome showed diverse chemical classes such as cinnamic acids, sesquiterpene lactones, flavonoids, and lignans. Linking the recorded metabolome to the previously reported cytotoxicity identified sesquiterpene lactones as the major contributors to this activity. To confirm our findings, bioassay-guided fractionation of C. lipii was adopted and led to the isolation of the sesquiterpene lactone cynaropicrin with an IC50 of 1.817 µM against the CCRF-CEM leukemia cell line. The adopted methodology highlighted the uniqueness of the constitutive metabolome of C. lipii and determined the sesquiterpene lactones to be the responsible cytotoxic metabolites.

Details

Language :
English
ISSN :
14203049
Volume :
28
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Molecules
Publication Type :
Academic Journal
Accession number :
edsdoj.2eba775523554197a2763bd89b2126bd
Document Type :
article
Full Text :
https://doi.org/10.3390/molecules28020674