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Pathogenesis and Current Treatment of Osteosarcoma: Perspectives for Future Therapies

Osteosarcoma is the most common primary malignant bone tumor in children and young adults. The standard-of-care curative treatment for osteosarcoma utilizes doxorubicin, cisplatin, and high-dose methotrexate, a standard that has not changed in more than 40 years. The development of patient-specific...

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Autores principales: Rathore, Richa, Van Tine, Brian A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000603/
https://www.ncbi.nlm.nih.gov/pubmed/33809018
http://dx.doi.org/10.3390/jcm10061182
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author Rathore, Richa
Van Tine, Brian A.
author_facet Rathore, Richa
Van Tine, Brian A.
author_sort Rathore, Richa
collection PubMed
description Osteosarcoma is the most common primary malignant bone tumor in children and young adults. The standard-of-care curative treatment for osteosarcoma utilizes doxorubicin, cisplatin, and high-dose methotrexate, a standard that has not changed in more than 40 years. The development of patient-specific therapies requires an in-depth understanding of the unique genetics and biology of the tumor. Here, we discuss the role of normal bone biology in osteosarcomagenesis, highlighting the factors that drive normal osteoblast production, as well as abnormal osteosarcoma development. We then describe the pathology and current standard of care of osteosarcoma. Given the complex heterogeneity of osteosarcoma tumors, we explore the development of novel therapeutics for osteosarcoma that encompass a series of molecular targets. This analysis of pathogenic mechanisms will shed light on promising avenues for future therapeutic research in osteosarcoma.
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spelling pubmed-80006032021-03-28 Pathogenesis and Current Treatment of Osteosarcoma: Perspectives for Future Therapies Rathore, Richa Van Tine, Brian A. J Clin Med Review Osteosarcoma is the most common primary malignant bone tumor in children and young adults. The standard-of-care curative treatment for osteosarcoma utilizes doxorubicin, cisplatin, and high-dose methotrexate, a standard that has not changed in more than 40 years. The development of patient-specific therapies requires an in-depth understanding of the unique genetics and biology of the tumor. Here, we discuss the role of normal bone biology in osteosarcomagenesis, highlighting the factors that drive normal osteoblast production, as well as abnormal osteosarcoma development. We then describe the pathology and current standard of care of osteosarcoma. Given the complex heterogeneity of osteosarcoma tumors, we explore the development of novel therapeutics for osteosarcoma that encompass a series of molecular targets. This analysis of pathogenic mechanisms will shed light on promising avenues for future therapeutic research in osteosarcoma. MDPI 2021-03-12 /pmc/articles/PMC8000603/ /pubmed/33809018 http://dx.doi.org/10.3390/jcm10061182 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Rathore, Richa
Van Tine, Brian A.
Pathogenesis and Current Treatment of Osteosarcoma: Perspectives for Future Therapies
title Pathogenesis and Current Treatment of Osteosarcoma: Perspectives for Future Therapies
title_full Pathogenesis and Current Treatment of Osteosarcoma: Perspectives for Future Therapies
title_fullStr Pathogenesis and Current Treatment of Osteosarcoma: Perspectives for Future Therapies
title_full_unstemmed Pathogenesis and Current Treatment of Osteosarcoma: Perspectives for Future Therapies
title_short Pathogenesis and Current Treatment of Osteosarcoma: Perspectives for Future Therapies
title_sort pathogenesis and current treatment of osteosarcoma: perspectives for future therapies
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8000603/
https://www.ncbi.nlm.nih.gov/pubmed/33809018
http://dx.doi.org/10.3390/jcm10061182
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