Cargando…

The Biology of Ewing Sarcoma

Objective. The goal of this study was to review the current literature on the biology of Ewing's sarcoma, including current treatments and the means by which an understanding of biological mechanisms could impact future treatments. Methods. A search of PubMed and The Cochrane Collaboration was...

Descripción completa

Detalles Bibliográficos
Autores principales: Ross, Keir A., Smyth, Niall A., Murawski, Christopher D., Kennedy, John G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549336/
https://www.ncbi.nlm.nih.gov/pubmed/23346417
http://dx.doi.org/10.1155/2013/759725
_version_ 1782256404620378112
author Ross, Keir A.
Smyth, Niall A.
Murawski, Christopher D.
Kennedy, John G.
author_facet Ross, Keir A.
Smyth, Niall A.
Murawski, Christopher D.
Kennedy, John G.
author_sort Ross, Keir A.
collection PubMed
description Objective. The goal of this study was to review the current literature on the biology of Ewing's sarcoma, including current treatments and the means by which an understanding of biological mechanisms could impact future treatments. Methods. A search of PubMed and The Cochrane Collaboration was performed. Both preclinical and clinical evidence was considered, but specific case reports were not. Primary research articles and reviews were analyzed with an emphasis on recent publications. Results. Ewing sarcoma is associated with specific chromosomal translocations and the resulting transcripts/proteins. Knowledge of the biology of Ewing sarcoma has been growing but has yet to significantly impact or produce new treatments. Localized cases have seen improvements in survival rates, but the same cannot be said of metastatic and recurrent cases. Standard surgical, radiation, and chemotherapy treatments are reaching their efficacy limits. Conclusion. Improving prognosis likely lies in advancing biomarkers and early diagnosis, determining a cell(s) of origin, and developing effective molecular therapeutics and antiangiogenic agents. Preclinical evidence suggests the utility of molecular therapies for Ewing sarcoma. Early clinical results also reveal potential for novel treatments but require further development and evaluation before widespread use can be advocated.
format Online
Article
Text
id pubmed-3549336
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Hindawi Publishing Corporation
record_format MEDLINE/PubMed
spelling pubmed-35493362013-01-23 The Biology of Ewing Sarcoma Ross, Keir A. Smyth, Niall A. Murawski, Christopher D. Kennedy, John G. ISRN Oncol Review Article Objective. The goal of this study was to review the current literature on the biology of Ewing's sarcoma, including current treatments and the means by which an understanding of biological mechanisms could impact future treatments. Methods. A search of PubMed and The Cochrane Collaboration was performed. Both preclinical and clinical evidence was considered, but specific case reports were not. Primary research articles and reviews were analyzed with an emphasis on recent publications. Results. Ewing sarcoma is associated with specific chromosomal translocations and the resulting transcripts/proteins. Knowledge of the biology of Ewing sarcoma has been growing but has yet to significantly impact or produce new treatments. Localized cases have seen improvements in survival rates, but the same cannot be said of metastatic and recurrent cases. Standard surgical, radiation, and chemotherapy treatments are reaching their efficacy limits. Conclusion. Improving prognosis likely lies in advancing biomarkers and early diagnosis, determining a cell(s) of origin, and developing effective molecular therapeutics and antiangiogenic agents. Preclinical evidence suggests the utility of molecular therapies for Ewing sarcoma. Early clinical results also reveal potential for novel treatments but require further development and evaluation before widespread use can be advocated. Hindawi Publishing Corporation 2013-01-10 /pmc/articles/PMC3549336/ /pubmed/23346417 http://dx.doi.org/10.1155/2013/759725 Text en Copyright © 2013 Keir A. Ross 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
Ross, Keir A.
Smyth, Niall A.
Murawski, Christopher D.
Kennedy, John G.
The Biology of Ewing Sarcoma
title The Biology of Ewing Sarcoma
title_full The Biology of Ewing Sarcoma
title_fullStr The Biology of Ewing Sarcoma
title_full_unstemmed The Biology of Ewing Sarcoma
title_short The Biology of Ewing Sarcoma
title_sort biology of ewing sarcoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3549336/
https://www.ncbi.nlm.nih.gov/pubmed/23346417
http://dx.doi.org/10.1155/2013/759725
work_keys_str_mv AT rosskeira thebiologyofewingsarcoma
AT smythnialla thebiologyofewingsarcoma
AT murawskichristopherd thebiologyofewingsarcoma
AT kennedyjohng thebiologyofewingsarcoma
AT rosskeira biologyofewingsarcoma
AT smythnialla biologyofewingsarcoma
AT murawskichristopherd biologyofewingsarcoma
AT kennedyjohng biologyofewingsarcoma