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Molecular Alterations Associated with Osteosarcoma Development

Osteosarcoma is the most frequent malignant primary bone tumor characterized by a high potency to form lung metastases which is the main cause of death. Unfortunately, the conventional chemotherapy is not fully effective on osteosarcoma metastases. The progression of a primary tumor to metastasis re...

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Detalles Bibliográficos
Autores principales: Ando, Kosei, Mori, Kanji, Verrecchia, Franck, Marc, Baud'huin, Rédini, Françoise, Heymann, Dominique
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3289857/
https://www.ncbi.nlm.nih.gov/pubmed/22448123
http://dx.doi.org/10.1155/2012/523432
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author Ando, Kosei
Mori, Kanji
Verrecchia, Franck
Marc, Baud'huin
Rédini, Françoise
Heymann, Dominique
author_facet Ando, Kosei
Mori, Kanji
Verrecchia, Franck
Marc, Baud'huin
Rédini, Françoise
Heymann, Dominique
author_sort Ando, Kosei
collection PubMed
description Osteosarcoma is the most frequent malignant primary bone tumor characterized by a high potency to form lung metastases which is the main cause of death. Unfortunately, the conventional chemotherapy is not fully effective on osteosarcoma metastases. The progression of a primary tumor to metastasis requires multiple processes, which are neovascularization, proliferation, invasion, survival in the bloodstream, apoptosis resistance, arrest at a distant organ, and outgrowth in secondary sites. Consequently, recent studies have revealed new insights into the molecular mechanisms of metastasis development. The understanding of the mechanism of molecular alterations can provide the identification of novel therapeutic targets and/or prognostic markers for osteosarcoma treatment to improve the clinical outcome.
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spelling pubmed-32898572012-03-23 Molecular Alterations Associated with Osteosarcoma Development Ando, Kosei Mori, Kanji Verrecchia, Franck Marc, Baud'huin Rédini, Françoise Heymann, Dominique Sarcoma Review Article Osteosarcoma is the most frequent malignant primary bone tumor characterized by a high potency to form lung metastases which is the main cause of death. Unfortunately, the conventional chemotherapy is not fully effective on osteosarcoma metastases. The progression of a primary tumor to metastasis requires multiple processes, which are neovascularization, proliferation, invasion, survival in the bloodstream, apoptosis resistance, arrest at a distant organ, and outgrowth in secondary sites. Consequently, recent studies have revealed new insights into the molecular mechanisms of metastasis development. The understanding of the mechanism of molecular alterations can provide the identification of novel therapeutic targets and/or prognostic markers for osteosarcoma treatment to improve the clinical outcome. Hindawi Publishing Corporation 2012 2012-02-15 /pmc/articles/PMC3289857/ /pubmed/22448123 http://dx.doi.org/10.1155/2012/523432 Text en Copyright © 2012 Kosei Ando et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ando, Kosei
Mori, Kanji
Verrecchia, Franck
Marc, Baud'huin
Rédini, Françoise
Heymann, Dominique
Molecular Alterations Associated with Osteosarcoma Development
title Molecular Alterations Associated with Osteosarcoma Development
title_full Molecular Alterations Associated with Osteosarcoma Development
title_fullStr Molecular Alterations Associated with Osteosarcoma Development
title_full_unstemmed Molecular Alterations Associated with Osteosarcoma Development
title_short Molecular Alterations Associated with Osteosarcoma Development
title_sort molecular alterations associated with osteosarcoma development
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3289857/
https://www.ncbi.nlm.nih.gov/pubmed/22448123
http://dx.doi.org/10.1155/2012/523432
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