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Can Denosumab be used in combination with Doxorubicin in Osteosarcoma?

Osteosarcoma is an aggressive bone tumor of the pediatric age. It is therefore important to improve conventional therapies (chemotherapy and surgery). Anticancer drugs often cause osteoporosis due to a misbalance of RANK/RANK-L/OPG pathway. Denosumab is a monoclonal antibody with high affinity and s...

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Autores principales: Punzo, Francesca, Tortora, Chiara, Argenziano, Maura, Pinto, Daniela Di, Pota, Elvira, Martino, Martina Di, Paola, Alessandra Di, Rossi, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367655/
https://www.ncbi.nlm.nih.gov/pubmed/32733647
http://dx.doi.org/10.18632/oncotarget.27669
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author Punzo, Francesca
Tortora, Chiara
Argenziano, Maura
Pinto, Daniela Di
Pota, Elvira
Martino, Martina Di
Paola, Alessandra Di
Rossi, Francesca
author_facet Punzo, Francesca
Tortora, Chiara
Argenziano, Maura
Pinto, Daniela Di
Pota, Elvira
Martino, Martina Di
Paola, Alessandra Di
Rossi, Francesca
author_sort Punzo, Francesca
collection PubMed
description Osteosarcoma is an aggressive bone tumor of the pediatric age. It is therefore important to improve conventional therapies (chemotherapy and surgery). Anticancer drugs often cause osteoporosis due to a misbalance of RANK/RANK-L/OPG pathway. Denosumab is a monoclonal antibody with high affinity and specificity to RANK-L, the ligand released by osteoblasts that enhances osteoclasts differentiation and bone resorption. It is used in osteoporosis and in other conditions characterized by bone mass loss. Doxorubicin is a chemotherapic drug used in several kinds of tumors, and also patients treated with it often develop osteoporosis. We investigated the effects of Denosumab alone and in combination with Doxorubicin, in two human osteosarcoma cell lines (MG63 and U-2 OS). We evaluated the effect of these treatments on apoptosis, cell cycle progression, invasion capacity and bone metabolism. We observed for the first time an anti-invasive effect of Denosumab in OS cells and confirmed its anti-osteoporotic activity also in Osteosarcoma. On the other hand, we demonstrate that Denosumab not only does not affect apoptosis and cell cycle progression, but when used in combination with Doxorubicin, it causes an unexpected reduction of its activity. These results indicate that the presence of Denosumab might inhibit the efficacy of the chemotherapic drug. In conclusion, while our results certainly support and confirm the efficacy of Denosumab in Osteoporosis, we discourage the use of Denosumab in addition to conventional chemotherapy in Osteosarcoma, even though, certainly further investigations are necessary to better clarify the clinical role of this monoclonal antibody in cancer.
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spelling pubmed-73676552020-07-29 Can Denosumab be used in combination with Doxorubicin in Osteosarcoma? Punzo, Francesca Tortora, Chiara Argenziano, Maura Pinto, Daniela Di Pota, Elvira Martino, Martina Di Paola, Alessandra Di Rossi, Francesca Oncotarget Research Paper Osteosarcoma is an aggressive bone tumor of the pediatric age. It is therefore important to improve conventional therapies (chemotherapy and surgery). Anticancer drugs often cause osteoporosis due to a misbalance of RANK/RANK-L/OPG pathway. Denosumab is a monoclonal antibody with high affinity and specificity to RANK-L, the ligand released by osteoblasts that enhances osteoclasts differentiation and bone resorption. It is used in osteoporosis and in other conditions characterized by bone mass loss. Doxorubicin is a chemotherapic drug used in several kinds of tumors, and also patients treated with it often develop osteoporosis. We investigated the effects of Denosumab alone and in combination with Doxorubicin, in two human osteosarcoma cell lines (MG63 and U-2 OS). We evaluated the effect of these treatments on apoptosis, cell cycle progression, invasion capacity and bone metabolism. We observed for the first time an anti-invasive effect of Denosumab in OS cells and confirmed its anti-osteoporotic activity also in Osteosarcoma. On the other hand, we demonstrate that Denosumab not only does not affect apoptosis and cell cycle progression, but when used in combination with Doxorubicin, it causes an unexpected reduction of its activity. These results indicate that the presence of Denosumab might inhibit the efficacy of the chemotherapic drug. In conclusion, while our results certainly support and confirm the efficacy of Denosumab in Osteoporosis, we discourage the use of Denosumab in addition to conventional chemotherapy in Osteosarcoma, even though, certainly further investigations are necessary to better clarify the clinical role of this monoclonal antibody in cancer. Impact Journals LLC 2020-07-14 /pmc/articles/PMC7367655/ /pubmed/32733647 http://dx.doi.org/10.18632/oncotarget.27669 Text en http://creativecommons.org/licenses/by/3.0/ Copyright: Punzo et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Punzo, Francesca
Tortora, Chiara
Argenziano, Maura
Pinto, Daniela Di
Pota, Elvira
Martino, Martina Di
Paola, Alessandra Di
Rossi, Francesca
Can Denosumab be used in combination with Doxorubicin in Osteosarcoma?
title Can Denosumab be used in combination with Doxorubicin in Osteosarcoma?
title_full Can Denosumab be used in combination with Doxorubicin in Osteosarcoma?
title_fullStr Can Denosumab be used in combination with Doxorubicin in Osteosarcoma?
title_full_unstemmed Can Denosumab be used in combination with Doxorubicin in Osteosarcoma?
title_short Can Denosumab be used in combination with Doxorubicin in Osteosarcoma?
title_sort can denosumab be used in combination with doxorubicin in osteosarcoma?
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7367655/
https://www.ncbi.nlm.nih.gov/pubmed/32733647
http://dx.doi.org/10.18632/oncotarget.27669
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