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MiR-4270 acts as a tumor suppressor by directly targeting Bcl-xL in human osteosarcoma cells
Chondrosarcomas and osteosarcomas are malignant bone tumors with a poor prognosis when unresectable or metastasized. Moreover, radiotherapy and chemotherapy could be ineffective. MiRNAs represent an alternative therapeutic approach. Based on high-throughput functional screening, we identified four m...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501397/ https://www.ncbi.nlm.nih.gov/pubmed/37719019 http://dx.doi.org/10.3389/fonc.2023.1220459 |
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author | Veys, Clément Boulouard, Flavie Benmoussa, Abderrahim Jammes, Manon Brotin, Emilie Rédini, Françoise Poulain, Laurent Gruchy, Nicolas Denoyelle, Christophe Legendre, Florence Galera, Philippe |
author_facet | Veys, Clément Boulouard, Flavie Benmoussa, Abderrahim Jammes, Manon Brotin, Emilie Rédini, Françoise Poulain, Laurent Gruchy, Nicolas Denoyelle, Christophe Legendre, Florence Galera, Philippe |
author_sort | Veys, Clément |
collection | PubMed |
description | Chondrosarcomas and osteosarcomas are malignant bone tumors with a poor prognosis when unresectable or metastasized. Moreover, radiotherapy and chemotherapy could be ineffective. MiRNAs represent an alternative therapeutic approach. Based on high-throughput functional screening, we identified four miRNAs with a potential antiproliferative effect on SW1353 chondrosarcoma cells. Individual functional validations were then performed in SW1353 cells, as well as in three osteosarcoma cell lines. The antiproliferative and cytotoxic effects of miRNAs were evaluated in comparison with a positive control, miR-342-5p. The cytotoxic effect of four selected miRNAs was not confirmed on SW1353 cells, but we unambiguously revealed that miR-4270 had a potent cytotoxic effect on HOS and MG-63 osteosarcoma cell lines, but not on SaOS-2 cell line. Furthermore, like miR-342-5p, miR-4270 induced apoptosis in these two cell lines. In addition, we provided the first report of Bcl-xL as a direct target of miR-4270. MiR-4270 also decreased the expression of the anti-apoptotic protein Mcl-1, and increased the expression of the pro-apoptotic protein Bak. Our findings demonstrated that miR-4270 has tumor suppressive activity in osteosarcoma cells, particularly through Bcl-xL downregulation. |
format | Online Article Text |
id | pubmed-10501397 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-105013972023-09-15 MiR-4270 acts as a tumor suppressor by directly targeting Bcl-xL in human osteosarcoma cells Veys, Clément Boulouard, Flavie Benmoussa, Abderrahim Jammes, Manon Brotin, Emilie Rédini, Françoise Poulain, Laurent Gruchy, Nicolas Denoyelle, Christophe Legendre, Florence Galera, Philippe Front Oncol Oncology Chondrosarcomas and osteosarcomas are malignant bone tumors with a poor prognosis when unresectable or metastasized. Moreover, radiotherapy and chemotherapy could be ineffective. MiRNAs represent an alternative therapeutic approach. Based on high-throughput functional screening, we identified four miRNAs with a potential antiproliferative effect on SW1353 chondrosarcoma cells. Individual functional validations were then performed in SW1353 cells, as well as in three osteosarcoma cell lines. The antiproliferative and cytotoxic effects of miRNAs were evaluated in comparison with a positive control, miR-342-5p. The cytotoxic effect of four selected miRNAs was not confirmed on SW1353 cells, but we unambiguously revealed that miR-4270 had a potent cytotoxic effect on HOS and MG-63 osteosarcoma cell lines, but not on SaOS-2 cell line. Furthermore, like miR-342-5p, miR-4270 induced apoptosis in these two cell lines. In addition, we provided the first report of Bcl-xL as a direct target of miR-4270. MiR-4270 also decreased the expression of the anti-apoptotic protein Mcl-1, and increased the expression of the pro-apoptotic protein Bak. Our findings demonstrated that miR-4270 has tumor suppressive activity in osteosarcoma cells, particularly through Bcl-xL downregulation. Frontiers Media S.A. 2023-08-31 /pmc/articles/PMC10501397/ /pubmed/37719019 http://dx.doi.org/10.3389/fonc.2023.1220459 Text en Copyright © 2023 Veys, Boulouard, Benmoussa, Jammes, Brotin, Rédini, Poulain, Gruchy, Denoyelle, Legendre and Galera https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Veys, Clément Boulouard, Flavie Benmoussa, Abderrahim Jammes, Manon Brotin, Emilie Rédini, Françoise Poulain, Laurent Gruchy, Nicolas Denoyelle, Christophe Legendre, Florence Galera, Philippe MiR-4270 acts as a tumor suppressor by directly targeting Bcl-xL in human osteosarcoma cells |
title | MiR-4270 acts as a tumor suppressor by directly targeting Bcl-xL in human osteosarcoma cells |
title_full | MiR-4270 acts as a tumor suppressor by directly targeting Bcl-xL in human osteosarcoma cells |
title_fullStr | MiR-4270 acts as a tumor suppressor by directly targeting Bcl-xL in human osteosarcoma cells |
title_full_unstemmed | MiR-4270 acts as a tumor suppressor by directly targeting Bcl-xL in human osteosarcoma cells |
title_short | MiR-4270 acts as a tumor suppressor by directly targeting Bcl-xL in human osteosarcoma cells |
title_sort | mir-4270 acts as a tumor suppressor by directly targeting bcl-xl in human osteosarcoma cells |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10501397/ https://www.ncbi.nlm.nih.gov/pubmed/37719019 http://dx.doi.org/10.3389/fonc.2023.1220459 |
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