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Alveolar Soft Part Sarcomas: Molecular Pathogenesis and Implications for Novel Targeted Therapies
Alveolar soft part sarcoma (ASPS) is a very rare soft tissue sarcoma which arises primarily in children and young adults. Despite its unique histology and well-characterized genetic translocation, many questions remain regarding the pathogenesis and treatment of this tumor type. Though collective cl...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337503/ https://www.ncbi.nlm.nih.gov/pubmed/22566752 http://dx.doi.org/10.1155/2012/428789 |
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author | Mitton, Bryan Federman, Noah |
author_facet | Mitton, Bryan Federman, Noah |
author_sort | Mitton, Bryan |
collection | PubMed |
description | Alveolar soft part sarcoma (ASPS) is a very rare soft tissue sarcoma which arises primarily in children and young adults. Despite its unique histology and well-characterized genetic translocation, many questions remain regarding the pathogenesis and treatment of this tumor type. Though collective clinical experience with this tumor type spans more than 60 years, there has been little progress made in treating this uncommon but frequently fatal disease. This paper focuses on the available data regarding its molecular pathogenesis and insights into targeted therapeutics as well as the results of clinical trials performed to date to hopefully improve the outcome of patients with this rare malignancy. |
format | Online Article Text |
id | pubmed-3337503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-33375032012-05-07 Alveolar Soft Part Sarcomas: Molecular Pathogenesis and Implications for Novel Targeted Therapies Mitton, Bryan Federman, Noah Sarcoma Review Article Alveolar soft part sarcoma (ASPS) is a very rare soft tissue sarcoma which arises primarily in children and young adults. Despite its unique histology and well-characterized genetic translocation, many questions remain regarding the pathogenesis and treatment of this tumor type. Though collective clinical experience with this tumor type spans more than 60 years, there has been little progress made in treating this uncommon but frequently fatal disease. This paper focuses on the available data regarding its molecular pathogenesis and insights into targeted therapeutics as well as the results of clinical trials performed to date to hopefully improve the outcome of patients with this rare malignancy. Hindawi Publishing Corporation 2012 2012-04-08 /pmc/articles/PMC3337503/ /pubmed/22566752 http://dx.doi.org/10.1155/2012/428789 Text en Copyright © 2012 B. Mitton and N. Federman. 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 Mitton, Bryan Federman, Noah Alveolar Soft Part Sarcomas: Molecular Pathogenesis and Implications for Novel Targeted Therapies |
title | Alveolar Soft Part Sarcomas: Molecular Pathogenesis and Implications for Novel Targeted Therapies |
title_full | Alveolar Soft Part Sarcomas: Molecular Pathogenesis and Implications for Novel Targeted Therapies |
title_fullStr | Alveolar Soft Part Sarcomas: Molecular Pathogenesis and Implications for Novel Targeted Therapies |
title_full_unstemmed | Alveolar Soft Part Sarcomas: Molecular Pathogenesis and Implications for Novel Targeted Therapies |
title_short | Alveolar Soft Part Sarcomas: Molecular Pathogenesis and Implications for Novel Targeted Therapies |
title_sort | alveolar soft part sarcomas: molecular pathogenesis and implications for novel targeted therapies |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3337503/ https://www.ncbi.nlm.nih.gov/pubmed/22566752 http://dx.doi.org/10.1155/2012/428789 |
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