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Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge Crambe tailliezi
Regulated cell death (RCD) results from the activation of one or more signal transduction modules both in physiological or pathological conditions. It is now established that RCD is involved in numerous human diseases, including cancer. As regulated cell death processes can be modulated by pharmacol...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836018/ https://www.ncbi.nlm.nih.gov/pubmed/31600933 http://dx.doi.org/10.3390/md17100569 |
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author | Nguyen, Thi-Ngoc-Dung Feizbakhsh, Omid Sfecci, Estelle Baratte, Blandine Delehouzé, Claire Garcia, Adrien Moulin, Corentin Colas, Pierre Ruchaud, Sandrine Mehiri, Mohamed Bach, Stéphane |
author_facet | Nguyen, Thi-Ngoc-Dung Feizbakhsh, Omid Sfecci, Estelle Baratte, Blandine Delehouzé, Claire Garcia, Adrien Moulin, Corentin Colas, Pierre Ruchaud, Sandrine Mehiri, Mohamed Bach, Stéphane |
author_sort | Nguyen, Thi-Ngoc-Dung |
collection | PubMed |
description | Regulated cell death (RCD) results from the activation of one or more signal transduction modules both in physiological or pathological conditions. It is now established that RCD is involved in numerous human diseases, including cancer. As regulated cell death processes can be modulated by pharmacological tools, the research reported here aims to characterize new marine compounds acting as RCD modulators. Protein kinases (PKs) are key signaling actors in various RCDs notably through the control of either mitosis (e.g., the PKs Aurora A and B) or necroptosis (e.g., RIPK1 and RIPK3). From the primary screening of 27 various extracts of marine organisms collected in the Mediterranean Sea, an extract and subsequently a purified high molecular weight compound dubbed P3, were isolated from the marine sponge Crambe tailliezi and characterized as a selective inhibitor of PKs Aurora A and B. Furthermore, P3 was shown to induce apoptosis and to decrease proliferation and mitotic index of human osteosarcoma U-2 OS cells. |
format | Online Article Text |
id | pubmed-6836018 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-68360182019-11-25 Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge Crambe tailliezi Nguyen, Thi-Ngoc-Dung Feizbakhsh, Omid Sfecci, Estelle Baratte, Blandine Delehouzé, Claire Garcia, Adrien Moulin, Corentin Colas, Pierre Ruchaud, Sandrine Mehiri, Mohamed Bach, Stéphane Mar Drugs Article Regulated cell death (RCD) results from the activation of one or more signal transduction modules both in physiological or pathological conditions. It is now established that RCD is involved in numerous human diseases, including cancer. As regulated cell death processes can be modulated by pharmacological tools, the research reported here aims to characterize new marine compounds acting as RCD modulators. Protein kinases (PKs) are key signaling actors in various RCDs notably through the control of either mitosis (e.g., the PKs Aurora A and B) or necroptosis (e.g., RIPK1 and RIPK3). From the primary screening of 27 various extracts of marine organisms collected in the Mediterranean Sea, an extract and subsequently a purified high molecular weight compound dubbed P3, were isolated from the marine sponge Crambe tailliezi and characterized as a selective inhibitor of PKs Aurora A and B. Furthermore, P3 was shown to induce apoptosis and to decrease proliferation and mitotic index of human osteosarcoma U-2 OS cells. MDPI 2019-10-09 /pmc/articles/PMC6836018/ /pubmed/31600933 http://dx.doi.org/10.3390/md17100569 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Nguyen, Thi-Ngoc-Dung Feizbakhsh, Omid Sfecci, Estelle Baratte, Blandine Delehouzé, Claire Garcia, Adrien Moulin, Corentin Colas, Pierre Ruchaud, Sandrine Mehiri, Mohamed Bach, Stéphane Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge Crambe tailliezi |
title | Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge Crambe tailliezi |
title_full | Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge Crambe tailliezi |
title_fullStr | Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge Crambe tailliezi |
title_full_unstemmed | Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge Crambe tailliezi |
title_short | Kinase-Based Screening of Marine Natural Extracts Leads to the Identification of a Cytotoxic High Molecular Weight Metabolite from the Mediterranean Sponge Crambe tailliezi |
title_sort | kinase-based screening of marine natural extracts leads to the identification of a cytotoxic high molecular weight metabolite from the mediterranean sponge crambe tailliezi |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6836018/ https://www.ncbi.nlm.nih.gov/pubmed/31600933 http://dx.doi.org/10.3390/md17100569 |
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