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Cytotoxic Compounds from Alcyoniidae: An Overview of the Last 30 Years

The octocoral family Alcyoniidae represents a rich source of bioactive substances with intriguing and unique structural features. This review aims to provide an updated overview of the compounds isolated from Alcyoniidae and displaying potential cytotoxic activity. In order to allow a better compari...

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Autores principales: Cerri, Federico, Saliu, Francesco, Maggioni, Davide, Montano, Simone, Seveso, Davide, Lavorano, Silvia, Zoia, Luca, Gosetti, Fabio, Lasagni, Marina, Orlandi, Marco, Taglialatela-Scafati, Orazio, Galli, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8874409/
https://www.ncbi.nlm.nih.gov/pubmed/35200663
http://dx.doi.org/10.3390/md20020134
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author Cerri, Federico
Saliu, Francesco
Maggioni, Davide
Montano, Simone
Seveso, Davide
Lavorano, Silvia
Zoia, Luca
Gosetti, Fabio
Lasagni, Marina
Orlandi, Marco
Taglialatela-Scafati, Orazio
Galli, Paolo
author_facet Cerri, Federico
Saliu, Francesco
Maggioni, Davide
Montano, Simone
Seveso, Davide
Lavorano, Silvia
Zoia, Luca
Gosetti, Fabio
Lasagni, Marina
Orlandi, Marco
Taglialatela-Scafati, Orazio
Galli, Paolo
author_sort Cerri, Federico
collection PubMed
description The octocoral family Alcyoniidae represents a rich source of bioactive substances with intriguing and unique structural features. This review aims to provide an updated overview of the compounds isolated from Alcyoniidae and displaying potential cytotoxic activity. In order to allow a better comparison among the bioactive compounds, we focused on molecules evaluated in vitro by using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay, by far the most widely used method to analyze cell proliferation and viability. Specifically, we surveyed the last thirty years of research, finding 153 papers reporting on 344 compounds with proven cytotoxicity. The data were organized in tables to provide a ranking of the most active compounds, to be exploited for the selection of the most promising candidates for further screening and pre-clinical evaluation as anti-cancer agents. Specifically, we found that (22S,24S)-24-methyl-22,25-epoxyfurost-5-ene-3β,20β-diol (16), 3β,11-dihydroxy-24-methylene-9,11-secocholestan-5-en-9-one (23), (24S)-ergostane-3β,5α,6β,25 tetraol (146), sinulerectadione (227), sinulerectol C (229), and cladieunicellin I (277) exhibited stronger cytotoxicity than their respective positive control and that their mechanism of action has not yet been further investigated.
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spelling pubmed-88744092022-02-26 Cytotoxic Compounds from Alcyoniidae: An Overview of the Last 30 Years Cerri, Federico Saliu, Francesco Maggioni, Davide Montano, Simone Seveso, Davide Lavorano, Silvia Zoia, Luca Gosetti, Fabio Lasagni, Marina Orlandi, Marco Taglialatela-Scafati, Orazio Galli, Paolo Mar Drugs Review The octocoral family Alcyoniidae represents a rich source of bioactive substances with intriguing and unique structural features. This review aims to provide an updated overview of the compounds isolated from Alcyoniidae and displaying potential cytotoxic activity. In order to allow a better comparison among the bioactive compounds, we focused on molecules evaluated in vitro by using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay, by far the most widely used method to analyze cell proliferation and viability. Specifically, we surveyed the last thirty years of research, finding 153 papers reporting on 344 compounds with proven cytotoxicity. The data were organized in tables to provide a ranking of the most active compounds, to be exploited for the selection of the most promising candidates for further screening and pre-clinical evaluation as anti-cancer agents. Specifically, we found that (22S,24S)-24-methyl-22,25-epoxyfurost-5-ene-3β,20β-diol (16), 3β,11-dihydroxy-24-methylene-9,11-secocholestan-5-en-9-one (23), (24S)-ergostane-3β,5α,6β,25 tetraol (146), sinulerectadione (227), sinulerectol C (229), and cladieunicellin I (277) exhibited stronger cytotoxicity than their respective positive control and that their mechanism of action has not yet been further investigated. MDPI 2022-02-11 /pmc/articles/PMC8874409/ /pubmed/35200663 http://dx.doi.org/10.3390/md20020134 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Cerri, Federico
Saliu, Francesco
Maggioni, Davide
Montano, Simone
Seveso, Davide
Lavorano, Silvia
Zoia, Luca
Gosetti, Fabio
Lasagni, Marina
Orlandi, Marco
Taglialatela-Scafati, Orazio
Galli, Paolo
Cytotoxic Compounds from Alcyoniidae: An Overview of the Last 30 Years
title Cytotoxic Compounds from Alcyoniidae: An Overview of the Last 30 Years
title_full Cytotoxic Compounds from Alcyoniidae: An Overview of the Last 30 Years
title_fullStr Cytotoxic Compounds from Alcyoniidae: An Overview of the Last 30 Years
title_full_unstemmed Cytotoxic Compounds from Alcyoniidae: An Overview of the Last 30 Years
title_short Cytotoxic Compounds from Alcyoniidae: An Overview of the Last 30 Years
title_sort cytotoxic compounds from alcyoniidae: an overview of the last 30 years
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8874409/
https://www.ncbi.nlm.nih.gov/pubmed/35200663
http://dx.doi.org/10.3390/md20020134
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