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Polyamine Biosynthetic Pathway as a Drug Target for Osteosarcoma Therapy

Osteosarcoma (OS) is the most common bone tumor in children. Polyamines (PAs) are ubiquitous cations involved in many cell processes including tumor development, invasion and metastasis. In other pediatric cancer models, inhibition of the PA biosynthesis pathway with ornithine decarboxylase (ODC) in...

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Autores principales: Weicht, Rebecca R., Schultz, Chad R., Geerts, Dirk, Uhl, Katie L., Bachmann, André S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165283/
https://www.ncbi.nlm.nih.gov/pubmed/30115881
http://dx.doi.org/10.3390/medsci6030065
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author Weicht, Rebecca R.
Schultz, Chad R.
Geerts, Dirk
Uhl, Katie L.
Bachmann, André S.
author_facet Weicht, Rebecca R.
Schultz, Chad R.
Geerts, Dirk
Uhl, Katie L.
Bachmann, André S.
author_sort Weicht, Rebecca R.
collection PubMed
description Osteosarcoma (OS) is the most common bone tumor in children. Polyamines (PAs) are ubiquitous cations involved in many cell processes including tumor development, invasion and metastasis. In other pediatric cancer models, inhibition of the PA biosynthesis pathway with ornithine decarboxylase (ODC) inhibitor alpha-difluoromethylornithine (DFMO) results in decreased cell proliferation and differentiation. In OS, the PA pathway has not been evaluated. DFMO is an attractive, orally administered drug, is well tolerated, can be given for prolonged periods, and is already used in pediatric patients. Three OS cell lines were used to study the cellular effects of PA inhibition with DFMO: MG-63, U-2 OS and Saos-2. Effects on proliferation were analyzed by cell count, flow cytometry-based cell cycle analysis and RealTime-Glo™ MT Cell Viability assays. Intracellular PA levels were measured with high-performance liquid chromatography (HPLC). Western blot analysis was used to evaluate cell differentiation. DFMO exposure resulted in significantly decreased cell proliferation in all cell lines. After treatment, intracellular spermidine levels were drastically decreased. Cell cycle arrest at G(2)/M was observed in U-2 OS and Saos-2. Cell differentiation was most prominent in MG-63 and U-2 OS as determined by increases in the terminal differentiation markers osteopontin and collagen 1a1. Cell proliferation continued to be suppressed for several days after removal of DFMO. Based on our findings, DFMO is a promising new adjunct to current osteosarcoma therapy in patients at high risk of relapse, such as those with poor necrosis at resection or those with metastatic or recurrent osteosarcoma. It is a well-tolerated oral drug that is currently in phase II clinical trials in pediatric neuroblastoma patients as a maintenance therapy. The same type of regimen may also improve outcomes in osteosarcoma patients in whom there have been essentially no medical advances in the last 30 years.
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spelling pubmed-61652832018-10-10 Polyamine Biosynthetic Pathway as a Drug Target for Osteosarcoma Therapy Weicht, Rebecca R. Schultz, Chad R. Geerts, Dirk Uhl, Katie L. Bachmann, André S. Med Sci (Basel) Article Osteosarcoma (OS) is the most common bone tumor in children. Polyamines (PAs) are ubiquitous cations involved in many cell processes including tumor development, invasion and metastasis. In other pediatric cancer models, inhibition of the PA biosynthesis pathway with ornithine decarboxylase (ODC) inhibitor alpha-difluoromethylornithine (DFMO) results in decreased cell proliferation and differentiation. In OS, the PA pathway has not been evaluated. DFMO is an attractive, orally administered drug, is well tolerated, can be given for prolonged periods, and is already used in pediatric patients. Three OS cell lines were used to study the cellular effects of PA inhibition with DFMO: MG-63, U-2 OS and Saos-2. Effects on proliferation were analyzed by cell count, flow cytometry-based cell cycle analysis and RealTime-Glo™ MT Cell Viability assays. Intracellular PA levels were measured with high-performance liquid chromatography (HPLC). Western blot analysis was used to evaluate cell differentiation. DFMO exposure resulted in significantly decreased cell proliferation in all cell lines. After treatment, intracellular spermidine levels were drastically decreased. Cell cycle arrest at G(2)/M was observed in U-2 OS and Saos-2. Cell differentiation was most prominent in MG-63 and U-2 OS as determined by increases in the terminal differentiation markers osteopontin and collagen 1a1. Cell proliferation continued to be suppressed for several days after removal of DFMO. Based on our findings, DFMO is a promising new adjunct to current osteosarcoma therapy in patients at high risk of relapse, such as those with poor necrosis at resection or those with metastatic or recurrent osteosarcoma. It is a well-tolerated oral drug that is currently in phase II clinical trials in pediatric neuroblastoma patients as a maintenance therapy. The same type of regimen may also improve outcomes in osteosarcoma patients in whom there have been essentially no medical advances in the last 30 years. MDPI 2018-08-16 /pmc/articles/PMC6165283/ /pubmed/30115881 http://dx.doi.org/10.3390/medsci6030065 Text en © 2018 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 Article
Weicht, Rebecca R.
Schultz, Chad R.
Geerts, Dirk
Uhl, Katie L.
Bachmann, André S.
Polyamine Biosynthetic Pathway as a Drug Target for Osteosarcoma Therapy
title Polyamine Biosynthetic Pathway as a Drug Target for Osteosarcoma Therapy
title_full Polyamine Biosynthetic Pathway as a Drug Target for Osteosarcoma Therapy
title_fullStr Polyamine Biosynthetic Pathway as a Drug Target for Osteosarcoma Therapy
title_full_unstemmed Polyamine Biosynthetic Pathway as a Drug Target for Osteosarcoma Therapy
title_short Polyamine Biosynthetic Pathway as a Drug Target for Osteosarcoma Therapy
title_sort polyamine biosynthetic pathway as a drug target for osteosarcoma therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6165283/
https://www.ncbi.nlm.nih.gov/pubmed/30115881
http://dx.doi.org/10.3390/medsci6030065
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