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Molecular alterations as target for therapy in metastatic osteosarcoma: a review of literature

Treating metastatic osteosarcoma (OS) remains a challenge in oncology. Current treatment strategies target the primary tumour rather than metastases and have a limited efficacy in the treatment of metastatic disease. Metastatic cells have specific features that render them less sensitive to therapy...

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Autores principales: PosthumaDeBoer, J., Witlox, M. A., Kaspers, G. J. L., van Royen, B. J.
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081058/
https://www.ncbi.nlm.nih.gov/pubmed/21461590
http://dx.doi.org/10.1007/s10585-011-9384-x
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author PosthumaDeBoer, J.
Witlox, M. A.
Kaspers, G. J. L.
van Royen, B. J.
author_facet PosthumaDeBoer, J.
Witlox, M. A.
Kaspers, G. J. L.
van Royen, B. J.
author_sort PosthumaDeBoer, J.
collection PubMed
description Treating metastatic osteosarcoma (OS) remains a challenge in oncology. Current treatment strategies target the primary tumour rather than metastases and have a limited efficacy in the treatment of metastatic disease. Metastatic cells have specific features that render them less sensitive to therapy and targeting these features might enhance the efficacy of current treatment. A detailed study of the biological characteristics and behaviour of metastatic OS cells may provide a rational basis for innovative treatment strategies. The aim of this review is to give an overview of the biological changes in metastatic OS cells and the preclinical and clinical efforts targeting the different steps in OS metastases and how these contribute to designing a metastasis directed treatment for OS.
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spelling pubmed-30810582011-06-06 Molecular alterations as target for therapy in metastatic osteosarcoma: a review of literature PosthumaDeBoer, J. Witlox, M. A. Kaspers, G. J. L. van Royen, B. J. Clin Exp Metastasis Review Treating metastatic osteosarcoma (OS) remains a challenge in oncology. Current treatment strategies target the primary tumour rather than metastases and have a limited efficacy in the treatment of metastatic disease. Metastatic cells have specific features that render them less sensitive to therapy and targeting these features might enhance the efficacy of current treatment. A detailed study of the biological characteristics and behaviour of metastatic OS cells may provide a rational basis for innovative treatment strategies. The aim of this review is to give an overview of the biological changes in metastatic OS cells and the preclinical and clinical efforts targeting the different steps in OS metastases and how these contribute to designing a metastasis directed treatment for OS. Springer Netherlands 2011-04-02 2011 /pmc/articles/PMC3081058/ /pubmed/21461590 http://dx.doi.org/10.1007/s10585-011-9384-x Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Review
PosthumaDeBoer, J.
Witlox, M. A.
Kaspers, G. J. L.
van Royen, B. J.
Molecular alterations as target for therapy in metastatic osteosarcoma: a review of literature
title Molecular alterations as target for therapy in metastatic osteosarcoma: a review of literature
title_full Molecular alterations as target for therapy in metastatic osteosarcoma: a review of literature
title_fullStr Molecular alterations as target for therapy in metastatic osteosarcoma: a review of literature
title_full_unstemmed Molecular alterations as target for therapy in metastatic osteosarcoma: a review of literature
title_short Molecular alterations as target for therapy in metastatic osteosarcoma: a review of literature
title_sort molecular alterations as target for therapy in metastatic osteosarcoma: a review of literature
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3081058/
https://www.ncbi.nlm.nih.gov/pubmed/21461590
http://dx.doi.org/10.1007/s10585-011-9384-x
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