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Proton pump inhibitor chemosensitization in human osteosarcoma: from the bench to the patients’ bed
BACKGROUND: Major goals in translational oncology are to reduce systemic toxicity of current anticancer strategies and improve effectiveness. An extremely efficient cancer cell mechanism to avoid and/or reduce the effects of highly cytotoxic drugs is the establishment of an acidic microenvironment,...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815282/ https://www.ncbi.nlm.nih.gov/pubmed/24156349 http://dx.doi.org/10.1186/1479-5876-11-268 |
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author | Ferrari, Stefano Perut, Francesca Fagioli, Franca Brach Del Prever, Adalberto Meazza, Cristina Parafioriti, Antonina Picci, Piero Gambarotti, Marco Avnet, Sofia Baldini, Nicola Fais, Stefano |
author_facet | Ferrari, Stefano Perut, Francesca Fagioli, Franca Brach Del Prever, Adalberto Meazza, Cristina Parafioriti, Antonina Picci, Piero Gambarotti, Marco Avnet, Sofia Baldini, Nicola Fais, Stefano |
author_sort | Ferrari, Stefano |
collection | PubMed |
description | BACKGROUND: Major goals in translational oncology are to reduce systemic toxicity of current anticancer strategies and improve effectiveness. An extremely efficient cancer cell mechanism to avoid and/or reduce the effects of highly cytotoxic drugs is the establishment of an acidic microenvironment, an hallmark of all malignant tumors. The H + −rich milieu that anticancer drugs meet once they get inside the tumor leads to their protonation and neutralization, therefore hindering their access into tumor cells. We have previously shown that proton pump inhibitors (PPI) may efficiently counterattack this tumor advantage leading to a consistent chemosensitization of tumors. In this study, we investigated the effects of PPI in chemosensitizing osteosarcoma. METHOD: MG-63 and Saos-2 cell lines were used as human osteosarcoma models. Cell proliferation after pretreatment with PPI and subsequent treatment with cisplatin was evaluated by using erythrosin B dye vital staining. Tumour growth was evaluated in xenograft treated with cisplatin after PPI pretreatment. Subsequently, a multi-centre historically controlled trial, was performed to evaluate the activity of a pre-treatment administration of PPIs as chemosensitizers during neoadjuvant chemotherapy based on methotrexate, cisplatin, and adriamycin. RESULTS: Preclinical experiments showed that PPI sensitize both human osteosarcoma cell lines and xenografts to cisplatin. A clinical study subsequently showed that pretreatment with PPI drug esomeprazole leads to an increase in the local effect of chemotherapy, as expressed by percentage of tumor necrosis. This was particularly evident in chondroblastic osteosarcoma, an histological subtype that normally shows a poor histological response. Notably, no significant increase in toxicity was recorded in PPI treated patients. CONCLUSION: This study provides the first evidence that PPI may be beneficially added to standard regimens in combination to conventional chemotherapy. |
format | Online Article Text |
id | pubmed-3815282 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-38152822013-11-03 Proton pump inhibitor chemosensitization in human osteosarcoma: from the bench to the patients’ bed Ferrari, Stefano Perut, Francesca Fagioli, Franca Brach Del Prever, Adalberto Meazza, Cristina Parafioriti, Antonina Picci, Piero Gambarotti, Marco Avnet, Sofia Baldini, Nicola Fais, Stefano J Transl Med Research BACKGROUND: Major goals in translational oncology are to reduce systemic toxicity of current anticancer strategies and improve effectiveness. An extremely efficient cancer cell mechanism to avoid and/or reduce the effects of highly cytotoxic drugs is the establishment of an acidic microenvironment, an hallmark of all malignant tumors. The H + −rich milieu that anticancer drugs meet once they get inside the tumor leads to their protonation and neutralization, therefore hindering their access into tumor cells. We have previously shown that proton pump inhibitors (PPI) may efficiently counterattack this tumor advantage leading to a consistent chemosensitization of tumors. In this study, we investigated the effects of PPI in chemosensitizing osteosarcoma. METHOD: MG-63 and Saos-2 cell lines were used as human osteosarcoma models. Cell proliferation after pretreatment with PPI and subsequent treatment with cisplatin was evaluated by using erythrosin B dye vital staining. Tumour growth was evaluated in xenograft treated with cisplatin after PPI pretreatment. Subsequently, a multi-centre historically controlled trial, was performed to evaluate the activity of a pre-treatment administration of PPIs as chemosensitizers during neoadjuvant chemotherapy based on methotrexate, cisplatin, and adriamycin. RESULTS: Preclinical experiments showed that PPI sensitize both human osteosarcoma cell lines and xenografts to cisplatin. A clinical study subsequently showed that pretreatment with PPI drug esomeprazole leads to an increase in the local effect of chemotherapy, as expressed by percentage of tumor necrosis. This was particularly evident in chondroblastic osteosarcoma, an histological subtype that normally shows a poor histological response. Notably, no significant increase in toxicity was recorded in PPI treated patients. CONCLUSION: This study provides the first evidence that PPI may be beneficially added to standard regimens in combination to conventional chemotherapy. BioMed Central 2013-10-24 /pmc/articles/PMC3815282/ /pubmed/24156349 http://dx.doi.org/10.1186/1479-5876-11-268 Text en Copyright © 2013 Ferrari et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Ferrari, Stefano Perut, Francesca Fagioli, Franca Brach Del Prever, Adalberto Meazza, Cristina Parafioriti, Antonina Picci, Piero Gambarotti, Marco Avnet, Sofia Baldini, Nicola Fais, Stefano Proton pump inhibitor chemosensitization in human osteosarcoma: from the bench to the patients’ bed |
title | Proton pump inhibitor chemosensitization in human osteosarcoma: from the bench to the patients’ bed |
title_full | Proton pump inhibitor chemosensitization in human osteosarcoma: from the bench to the patients’ bed |
title_fullStr | Proton pump inhibitor chemosensitization in human osteosarcoma: from the bench to the patients’ bed |
title_full_unstemmed | Proton pump inhibitor chemosensitization in human osteosarcoma: from the bench to the patients’ bed |
title_short | Proton pump inhibitor chemosensitization in human osteosarcoma: from the bench to the patients’ bed |
title_sort | proton pump inhibitor chemosensitization in human osteosarcoma: from the bench to the patients’ bed |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3815282/ https://www.ncbi.nlm.nih.gov/pubmed/24156349 http://dx.doi.org/10.1186/1479-5876-11-268 |
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