An Integrated Strategy of UHPLC-ESI-MS/MS Combined with Bioactivity-Based Molecular Networking for Identification of Antitumoral Withanolides from Athenaea fasciculata (Vell.) I.M.C. Rodrigues & Stehmann

Author:

Marques André Mesquita1ORCID,Brito Lavinia de Carvalho1,Mendonça Simony Carvalho2,Gomes Brendo Araujo2ORCID,Camillo Flávia da Cunha1,Silva Gustavo Werneck de Souza e3ORCID,Sampaio André Luiz Franco3ORCID,Leitão Suzana Guimarães2ORCID,Figueiredo Maria Raquel1

Affiliation:

1. Department of Natural Products, Pharmaceutical Technology Institute, Farmanguinhos, Fiocruz, Sizenando Nabuco 100 st, Manguinhos, Rio de Janeiro 21041-250, Brazil

2. Department of Natural Products and Food, Faculty of Pharmacy, Center of Health Sciences (CCS), Federal University of Rio de Janeiro, Rio de Janeiro 21941-902, Brazil

3. Laboratory of Molecular Pharmacology, Pharmaceutical Technology Institute, Farmanguinhos, Fiocruz, Avenida Brasil 4365, Manguinhos, Rio de Janeiro 21041-250, Brazil

Abstract

Background: Athenaea fasciculata, a Brazilian native species from the Solanaceae family, is recognized as a promising source of bioactive withanolides, particularly Aurelianolide A and B, which exhibit significant antitumoral activities. Despite its potential, research on the chemical constituents of this species remains limited. This study aimed to dereplicate extracts and partitions of A. fasciculata to streamline the discovery of bioactive withanolides. Methods: Using ultra-high-performance liquid chromatography–tandem mass spectrometry (UHPLC-MS/MS), various extracts—including n-hexane, methanol, and ethanol—were analyzed, and their mass spectrometry data were processed through the GNPS platform for the generation of molecular networking. The results indicated that crude extracts displayed comparable cytotoxicity against Jurkat cells, by treatment at 150 µg/mL, while alcoholic extracts achieved approximately 80% inhibition of K562 cells and K562-Lucena 1 at the same concentration. Notably, the dichloromethane partition exhibited the highest cytotoxicity across leukemia cell lines, particularly against Jurkat cells (IC50 = 14.34 µg/mL). A total of 22 compounds were annotated by manual inspection and different libraries, with six of them demonstrating significant cytotoxic effects. Conclusions: This research underscores the therapeutic potential of A. fasciculata and highlights the effectiveness of integrating advanced analytical methods in drug discovery, paving the way for further exploration of its bioactive compounds.

Funder

Conselho Nacional de Pesquisa

Publisher

MDPI AG

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