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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Neoplasia Press
2022
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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. |
format | Online Article Text |
id | pubmed-8956928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Neoplasia Press |
record_format | MEDLINE/PubMed |
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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