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Force-feeding malignant mesothelioma stem-cell like with exosome-delivered miR-126 induces tumour cell killing

Malignant pleural mesothelioma (MPM) is an aggressive tumour resistant to treatments. It has been postulated that cancer stem cells (CSCs) persist in tumours causing relapse after multimodality treatment. In the present study, a novel miRNA-based therapy approach is proposed. MPM-derived spheroids h...

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Detalles Bibliográficos
Autores principales: Monaco, Federica, De Conti, Laura, Vodret, Simone, Zanotta, Nunzia, Comar, Manola, Manzotti, Sandra, Rubini, Corrado, Graciotti, Laura, Fulgenzi, Gianluca, Bovenzi, Massimo, Baralle, Marco, Tomasetti, Marco, Santarelli, Lory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Neoplasia Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956928/
https://www.ncbi.nlm.nih.gov/pubmed/35334283
http://dx.doi.org/10.1016/j.tranon.2022.101400
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author Monaco, Federica
De Conti, Laura
Vodret, Simone
Zanotta, Nunzia
Comar, Manola
Manzotti, Sandra
Rubini, Corrado
Graciotti, Laura
Fulgenzi, Gianluca
Bovenzi, Massimo
Baralle, Marco
Tomasetti, Marco
Santarelli, Lory
author_facet Monaco, Federica
De Conti, Laura
Vodret, Simone
Zanotta, Nunzia
Comar, Manola
Manzotti, Sandra
Rubini, Corrado
Graciotti, Laura
Fulgenzi, Gianluca
Bovenzi, Massimo
Baralle, Marco
Tomasetti, Marco
Santarelli, Lory
author_sort Monaco, Federica
collection PubMed
description Malignant pleural mesothelioma (MPM) is an aggressive tumour resistant to treatments. It has been postulated that cancer stem cells (CSCs) persist in tumours causing relapse after multimodality treatment. In the present study, a novel miRNA-based therapy approach is proposed. MPM-derived spheroids have been treated with exosome-delivered miR-126 (exo-miR) and evaluated for their anticancer effect. The exo-miR treatment increased MPM stem-cell like stemness and inhibited cell proliferation. However, at a prolonged time, the up taken miR-126 was released by the cells themselves through exosomes; the inhibition of exosome release by an exosome release inhibitor GW4869 induced miR-126 intracellular accumulation leading to massive cell death and in vivo tumour growth arrest. Autophagy is involved in these processes; miR-126 accumulation induced a protective autophagy and the inhibition of this process by GW4869 generates a metabolic crisis that promotes necroptosis, which was associated with PARP-1 over-expression and cyt-c and AIF release. Here, for the first time, we proposed a therapy against CSCs, a heterogeneous cell population involved in cancer development and relapse.
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spelling pubmed-89569282022-04-07 Force-feeding malignant mesothelioma stem-cell like with exosome-delivered miR-126 induces tumour cell killing Monaco, Federica De Conti, Laura Vodret, Simone Zanotta, Nunzia Comar, Manola Manzotti, Sandra Rubini, Corrado Graciotti, Laura Fulgenzi, Gianluca Bovenzi, Massimo Baralle, Marco Tomasetti, Marco Santarelli, Lory Transl Oncol Original Research Malignant pleural mesothelioma (MPM) is an aggressive tumour resistant to treatments. It has been postulated that cancer stem cells (CSCs) persist in tumours causing relapse after multimodality treatment. In the present study, a novel miRNA-based therapy approach is proposed. MPM-derived spheroids have been treated with exosome-delivered miR-126 (exo-miR) and evaluated for their anticancer effect. The exo-miR treatment increased MPM stem-cell like stemness and inhibited cell proliferation. However, at a prolonged time, the up taken miR-126 was released by the cells themselves through exosomes; the inhibition of exosome release by an exosome release inhibitor GW4869 induced miR-126 intracellular accumulation leading to massive cell death and in vivo tumour growth arrest. Autophagy is involved in these processes; miR-126 accumulation induced a protective autophagy and the inhibition of this process by GW4869 generates a metabolic crisis that promotes necroptosis, which was associated with PARP-1 over-expression and cyt-c and AIF release. Here, for the first time, we proposed a therapy against CSCs, a heterogeneous cell population involved in cancer development and relapse. Neoplasia Press 2022-03-23 /pmc/articles/PMC8956928/ /pubmed/35334283 http://dx.doi.org/10.1016/j.tranon.2022.101400 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Research
Monaco, Federica
De Conti, Laura
Vodret, Simone
Zanotta, Nunzia
Comar, Manola
Manzotti, Sandra
Rubini, Corrado
Graciotti, Laura
Fulgenzi, Gianluca
Bovenzi, Massimo
Baralle, Marco
Tomasetti, Marco
Santarelli, Lory
Force-feeding malignant mesothelioma stem-cell like with exosome-delivered miR-126 induces tumour cell killing
title Force-feeding malignant mesothelioma stem-cell like with exosome-delivered miR-126 induces tumour cell killing
title_full Force-feeding malignant mesothelioma stem-cell like with exosome-delivered miR-126 induces tumour cell killing
title_fullStr Force-feeding malignant mesothelioma stem-cell like with exosome-delivered miR-126 induces tumour cell killing
title_full_unstemmed Force-feeding malignant mesothelioma stem-cell like with exosome-delivered miR-126 induces tumour cell killing
title_short Force-feeding malignant mesothelioma stem-cell like with exosome-delivered miR-126 induces tumour cell killing
title_sort force-feeding malignant mesothelioma stem-cell like with exosome-delivered mir-126 induces tumour cell killing
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956928/
https://www.ncbi.nlm.nih.gov/pubmed/35334283
http://dx.doi.org/10.1016/j.tranon.2022.101400
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