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Chlortetracycline, a Novel Arf Inhibitor That Decreases the Arf6-Dependent Invasive Properties of Breast Cancer Cells

Breast cancer is a major disease for women worldwide, where mortality is associated with tumour cell dissemination to distant organs. While the number of efficient anticancer therapies increased in the past 20 years, treatments targeting the invasive properties of metastatic tumour cells are still a...

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Autores principales: Macia, Eric, Vazquez-Rojas, Monserrat, Robiolo, Alessia, Fayad, Racha, Abélanet, Sophie, Mus-Veteau, Isabelle, Fontaine-Vive, Fabien, Mehiri, Mohamed, Luton, Frédéric, Franco, Michel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917842/
https://www.ncbi.nlm.nih.gov/pubmed/33673086
http://dx.doi.org/10.3390/molecules26040969
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author Macia, Eric
Vazquez-Rojas, Monserrat
Robiolo, Alessia
Fayad, Racha
Abélanet, Sophie
Mus-Veteau, Isabelle
Fontaine-Vive, Fabien
Mehiri, Mohamed
Luton, Frédéric
Franco, Michel
author_facet Macia, Eric
Vazquez-Rojas, Monserrat
Robiolo, Alessia
Fayad, Racha
Abélanet, Sophie
Mus-Veteau, Isabelle
Fontaine-Vive, Fabien
Mehiri, Mohamed
Luton, Frédéric
Franco, Michel
author_sort Macia, Eric
collection PubMed
description Breast cancer is a major disease for women worldwide, where mortality is associated with tumour cell dissemination to distant organs. While the number of efficient anticancer therapies increased in the past 20 years, treatments targeting the invasive properties of metastatic tumour cells are still awaited. Various studies analysing invasive breast cancer cell lines have demonstrated that Arf6 is an important player of the migratory and invasive processes. These observations make Arf6 and its regulators potential therapeutic targets. As of today, no drug effective against Arf6 has been identified, with one explanation being that the activation of Arf6 is dependent on the presence of lipid membranes that are rarely included in drug screening. To overcome this issue we have set up a fluorescence-based high throughput screening that follows overtime the activation of Arf6 at the surface of lipid membranes. Using this unique screening assay, we isolated several compounds that affect Arf6 activation, among which the antibiotic chlortetracycline (CTC) appeared to be the most promising. In this report, we describe CTC in vitro biochemical characterization and show that it blocks both the Arf6-stimulated collective migration and cell invasion in a 3D collagen I gel of the invasive breast cancer cell line MDA-MB-231. Thus, CTC appears as a promising hit to target deadly metastatic dissemination and a powerful tool to unravel the molecular mechanisms of Arf6-mediated invasive processes.
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spelling pubmed-79178422021-03-02 Chlortetracycline, a Novel Arf Inhibitor That Decreases the Arf6-Dependent Invasive Properties of Breast Cancer Cells Macia, Eric Vazquez-Rojas, Monserrat Robiolo, Alessia Fayad, Racha Abélanet, Sophie Mus-Veteau, Isabelle Fontaine-Vive, Fabien Mehiri, Mohamed Luton, Frédéric Franco, Michel Molecules Article Breast cancer is a major disease for women worldwide, where mortality is associated with tumour cell dissemination to distant organs. While the number of efficient anticancer therapies increased in the past 20 years, treatments targeting the invasive properties of metastatic tumour cells are still awaited. Various studies analysing invasive breast cancer cell lines have demonstrated that Arf6 is an important player of the migratory and invasive processes. These observations make Arf6 and its regulators potential therapeutic targets. As of today, no drug effective against Arf6 has been identified, with one explanation being that the activation of Arf6 is dependent on the presence of lipid membranes that are rarely included in drug screening. To overcome this issue we have set up a fluorescence-based high throughput screening that follows overtime the activation of Arf6 at the surface of lipid membranes. Using this unique screening assay, we isolated several compounds that affect Arf6 activation, among which the antibiotic chlortetracycline (CTC) appeared to be the most promising. In this report, we describe CTC in vitro biochemical characterization and show that it blocks both the Arf6-stimulated collective migration and cell invasion in a 3D collagen I gel of the invasive breast cancer cell line MDA-MB-231. Thus, CTC appears as a promising hit to target deadly metastatic dissemination and a powerful tool to unravel the molecular mechanisms of Arf6-mediated invasive processes. MDPI 2021-02-12 /pmc/articles/PMC7917842/ /pubmed/33673086 http://dx.doi.org/10.3390/molecules26040969 Text en © 2021 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
Macia, Eric
Vazquez-Rojas, Monserrat
Robiolo, Alessia
Fayad, Racha
Abélanet, Sophie
Mus-Veteau, Isabelle
Fontaine-Vive, Fabien
Mehiri, Mohamed
Luton, Frédéric
Franco, Michel
Chlortetracycline, a Novel Arf Inhibitor That Decreases the Arf6-Dependent Invasive Properties of Breast Cancer Cells
title Chlortetracycline, a Novel Arf Inhibitor That Decreases the Arf6-Dependent Invasive Properties of Breast Cancer Cells
title_full Chlortetracycline, a Novel Arf Inhibitor That Decreases the Arf6-Dependent Invasive Properties of Breast Cancer Cells
title_fullStr Chlortetracycline, a Novel Arf Inhibitor That Decreases the Arf6-Dependent Invasive Properties of Breast Cancer Cells
title_full_unstemmed Chlortetracycline, a Novel Arf Inhibitor That Decreases the Arf6-Dependent Invasive Properties of Breast Cancer Cells
title_short Chlortetracycline, a Novel Arf Inhibitor That Decreases the Arf6-Dependent Invasive Properties of Breast Cancer Cells
title_sort chlortetracycline, a novel arf inhibitor that decreases the arf6-dependent invasive properties of breast cancer cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7917842/
https://www.ncbi.nlm.nih.gov/pubmed/33673086
http://dx.doi.org/10.3390/molecules26040969
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