In VitroGrowth Inhibitory Activities of Natural Products from Irciniid Sponges against Cancer Cells: A Comparative Study

Author:

BenRedjem Romdhane Yosr1,Elbour Monia1,Carbone Marianna2,Ciavatta Maria Letizia2,Gavagnin Margherita2,Mathieu Véronique3,Lefranc Florence4,Ktari Leila1,Ben Mustapha Karim1,Boudabous Abdellatif5,Kiss Robert3,Mollo Ernesto2ORCID

Affiliation:

1. Institut National des Sciences et Technologies de la Mer (INSTM), Salammbô, 2025 Tunis, Tunisia

2. Consiglio Nazionale delle Ricerche (CNR), Istituto di Chimica Biomolecolare (ICB), 80078 Pozzuoli, Italy

3. Laboratoire de Cancérologie et de Toxicologie Expérimentale, Faculté de Pharmacie, Université Libre de Bruxelles (ULB), 1050 Brussels, Belgium

4. Service de Neurochirurgie, Hôpital Erasme, ULB, 1070 Brussels, Belgium

5. Laboratoire des Microorganismes et Biomolécules actives, Faculté des Sciences de Tunis, 2092 Tunis, Tunisia

Abstract

Marine sponges of the Irciniidae family contain both bioactive furanosesterterpene tetronic acids (FTAs) and prenylated hydroquinones (PHQs). Both classes of compounds are known for their anti-inflammatory, antioxidant, and antimicrobial properties and known to display growth inhibitory effects against various human tumor cell lines. However, the different experimental conditions of the reportedin vitrobioassays, carried out on different cancer cell lines within separate studies, prevent realistic actual discrimination between the two classes of compounds from being carried out in terms of growth inhibitory effects. In the present work, a chemical investigation of irciniid sponges from Tunisian coasts led to the purification of three known FTAs and three known PHQs. Thein vitrogrowth inhibitory properties of the six purified compounds have been evaluated in the same experiment in a panel of five human and one murine cancer cell lines displaying various levels of sensitivity to proapoptotic stimuli. Surprisingly, FTAs and PHQs elicited distinct profiles of growth inhibitory-responses, differing by one to two orders of magnitude in favor of the PHQs in all cell lines. The obtained comparative results are discussed in the light of a better selection of drug candidates from natural sources.

Funder

Ministère de l’Enseignement Supérieur, de la Recherche Scientifique et des Technologies de l'Information et de la Communication

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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