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Rapid Screening of Novel Agents for Combination Therapy in Sarcomas

For patients with sarcoma, metastatic disease remains very difficult to cure, and outcomes remain less than optimal. Treatment options have not largely changed, although some promising gains have been made with single agents in specific subtypes with the use of targeted agents. Here, we developed a...

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Autores principales: Cubitt, Christopher L., Menth, Jiliana, Dawson, Jana, Martinez, Gary V., Foroutan, Parastou, Morse, David L., Bui, Marilyn M., Letson, G. Douglas, Sullivan, Daniel M., Reed, Damon R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3824404/
https://www.ncbi.nlm.nih.gov/pubmed/24282374
http://dx.doi.org/10.1155/2013/365723
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author Cubitt, Christopher L.
Menth, Jiliana
Dawson, Jana
Martinez, Gary V.
Foroutan, Parastou
Morse, David L.
Bui, Marilyn M.
Letson, G. Douglas
Sullivan, Daniel M.
Reed, Damon R.
author_facet Cubitt, Christopher L.
Menth, Jiliana
Dawson, Jana
Martinez, Gary V.
Foroutan, Parastou
Morse, David L.
Bui, Marilyn M.
Letson, G. Douglas
Sullivan, Daniel M.
Reed, Damon R.
author_sort Cubitt, Christopher L.
collection PubMed
description For patients with sarcoma, metastatic disease remains very difficult to cure, and outcomes remain less than optimal. Treatment options have not largely changed, although some promising gains have been made with single agents in specific subtypes with the use of targeted agents. Here, we developed a system to investigate synergy of combinations of targeted and cytotoxic agents in a panel of sarcoma cell lines. Agents were investigated alone and in combination with varying dose ratios. Dose-response curves were analyzed for synergy using methods derived from Chou and Talalay (1984). A promising combination, dasatinib and triciribine, was explored in a murine model using the A673 cell line, and tumors were evaluated by MRI and histology for therapy effect. We found that histone deacetylase inhibitors were synergistic with etoposide, dasatinib, and Akt inhibitors across cell lines. Sorafenib and topotecan demonstrated a mixed response. Our systematic drug screening method allowed us to screen a large number of combinations of sarcoma agents. This method can be easily modified to accommodate other cell line models, and confirmatory assays, such as animal experiments, can provide excellent preclinical data to inform clinical trials for these rare malignancies.
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spelling pubmed-38244042013-11-26 Rapid Screening of Novel Agents for Combination Therapy in Sarcomas Cubitt, Christopher L. Menth, Jiliana Dawson, Jana Martinez, Gary V. Foroutan, Parastou Morse, David L. Bui, Marilyn M. Letson, G. Douglas Sullivan, Daniel M. Reed, Damon R. Sarcoma Research Article For patients with sarcoma, metastatic disease remains very difficult to cure, and outcomes remain less than optimal. Treatment options have not largely changed, although some promising gains have been made with single agents in specific subtypes with the use of targeted agents. Here, we developed a system to investigate synergy of combinations of targeted and cytotoxic agents in a panel of sarcoma cell lines. Agents were investigated alone and in combination with varying dose ratios. Dose-response curves were analyzed for synergy using methods derived from Chou and Talalay (1984). A promising combination, dasatinib and triciribine, was explored in a murine model using the A673 cell line, and tumors were evaluated by MRI and histology for therapy effect. We found that histone deacetylase inhibitors were synergistic with etoposide, dasatinib, and Akt inhibitors across cell lines. Sorafenib and topotecan demonstrated a mixed response. Our systematic drug screening method allowed us to screen a large number of combinations of sarcoma agents. This method can be easily modified to accommodate other cell line models, and confirmatory assays, such as animal experiments, can provide excellent preclinical data to inform clinical trials for these rare malignancies. Hindawi Publishing Corporation 2013 2013-10-24 /pmc/articles/PMC3824404/ /pubmed/24282374 http://dx.doi.org/10.1155/2013/365723 Text en Copyright © 2013 Christopher L. Cubitt 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 Research Article
Cubitt, Christopher L.
Menth, Jiliana
Dawson, Jana
Martinez, Gary V.
Foroutan, Parastou
Morse, David L.
Bui, Marilyn M.
Letson, G. Douglas
Sullivan, Daniel M.
Reed, Damon R.
Rapid Screening of Novel Agents for Combination Therapy in Sarcomas
title Rapid Screening of Novel Agents for Combination Therapy in Sarcomas
title_full Rapid Screening of Novel Agents for Combination Therapy in Sarcomas
title_fullStr Rapid Screening of Novel Agents for Combination Therapy in Sarcomas
title_full_unstemmed Rapid Screening of Novel Agents for Combination Therapy in Sarcomas
title_short Rapid Screening of Novel Agents for Combination Therapy in Sarcomas
title_sort rapid screening of novel agents for combination therapy in sarcomas
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3824404/
https://www.ncbi.nlm.nih.gov/pubmed/24282374
http://dx.doi.org/10.1155/2013/365723
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