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A multiplex preclinical model for adenoid cystic carcinoma of the salivary gland identifies regorafenib as a potential therapeutic drug

Adenoid cystic carcinomas (ACC) are rare salivary gland cancers with a high incidence of metastases. In order to study this tumor type, a reliable model system exhibiting the molecular features of this tumor is critical, but none exists, thereby inhibiting in-vitro studies and the analysis of metast...

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Autores principales: Chen, Chen, Choudhury, Sujata, Wangsa, Darawalee, Lescott, Chamille J., Wilkins, Devan J., Sripadhan, Praathibha, Liu, Xuefeng, Wangsa, Danny, Ried, Thomas, Moskaluk, Christopher, Wick, Michael J., Glasgow, Eric, Schlegel, Richard, Agarwal, Seema
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595986/
https://www.ncbi.nlm.nih.gov/pubmed/28900283
http://dx.doi.org/10.1038/s41598-017-11764-2
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author Chen, Chen
Choudhury, Sujata
Wangsa, Darawalee
Lescott, Chamille J.
Wilkins, Devan J.
Sripadhan, Praathibha
Liu, Xuefeng
Wangsa, Danny
Ried, Thomas
Moskaluk, Christopher
Wick, Michael J.
Glasgow, Eric
Schlegel, Richard
Agarwal, Seema
author_facet Chen, Chen
Choudhury, Sujata
Wangsa, Darawalee
Lescott, Chamille J.
Wilkins, Devan J.
Sripadhan, Praathibha
Liu, Xuefeng
Wangsa, Danny
Ried, Thomas
Moskaluk, Christopher
Wick, Michael J.
Glasgow, Eric
Schlegel, Richard
Agarwal, Seema
author_sort Chen, Chen
collection PubMed
description Adenoid cystic carcinomas (ACC) are rare salivary gland cancers with a high incidence of metastases. In order to study this tumor type, a reliable model system exhibiting the molecular features of this tumor is critical, but none exists, thereby inhibiting in-vitro studies and the analysis of metastatic behavior. To address this deficiency, we have coupled an efficient method to establish tumor cell cultures, conditional reprogramming (CR), with a rapid, reproducible and robust in-vivo zebrafish model. We have established cell cultures from two individual ACC PDX tumors that maintain the characteristic MYB translocation. Additional mutations found in one ACC culture also seen in the PDX tumor. Finally, the CR/zebrafish model mirrors the PDX mouse model and identifies regorafenib as a potential therapeutic drug to treat this cancer type that mimic the drug sensitivity profile in PDX model, further confirming the unique advantages of multiplex system.
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spelling pubmed-55959862017-09-15 A multiplex preclinical model for adenoid cystic carcinoma of the salivary gland identifies regorafenib as a potential therapeutic drug Chen, Chen Choudhury, Sujata Wangsa, Darawalee Lescott, Chamille J. Wilkins, Devan J. Sripadhan, Praathibha Liu, Xuefeng Wangsa, Danny Ried, Thomas Moskaluk, Christopher Wick, Michael J. Glasgow, Eric Schlegel, Richard Agarwal, Seema Sci Rep Article Adenoid cystic carcinomas (ACC) are rare salivary gland cancers with a high incidence of metastases. In order to study this tumor type, a reliable model system exhibiting the molecular features of this tumor is critical, but none exists, thereby inhibiting in-vitro studies and the analysis of metastatic behavior. To address this deficiency, we have coupled an efficient method to establish tumor cell cultures, conditional reprogramming (CR), with a rapid, reproducible and robust in-vivo zebrafish model. We have established cell cultures from two individual ACC PDX tumors that maintain the characteristic MYB translocation. Additional mutations found in one ACC culture also seen in the PDX tumor. Finally, the CR/zebrafish model mirrors the PDX mouse model and identifies regorafenib as a potential therapeutic drug to treat this cancer type that mimic the drug sensitivity profile in PDX model, further confirming the unique advantages of multiplex system. Nature Publishing Group UK 2017-09-12 /pmc/articles/PMC5595986/ /pubmed/28900283 http://dx.doi.org/10.1038/s41598-017-11764-2 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Chen, Chen
Choudhury, Sujata
Wangsa, Darawalee
Lescott, Chamille J.
Wilkins, Devan J.
Sripadhan, Praathibha
Liu, Xuefeng
Wangsa, Danny
Ried, Thomas
Moskaluk, Christopher
Wick, Michael J.
Glasgow, Eric
Schlegel, Richard
Agarwal, Seema
A multiplex preclinical model for adenoid cystic carcinoma of the salivary gland identifies regorafenib as a potential therapeutic drug
title A multiplex preclinical model for adenoid cystic carcinoma of the salivary gland identifies regorafenib as a potential therapeutic drug
title_full A multiplex preclinical model for adenoid cystic carcinoma of the salivary gland identifies regorafenib as a potential therapeutic drug
title_fullStr A multiplex preclinical model for adenoid cystic carcinoma of the salivary gland identifies regorafenib as a potential therapeutic drug
title_full_unstemmed A multiplex preclinical model for adenoid cystic carcinoma of the salivary gland identifies regorafenib as a potential therapeutic drug
title_short A multiplex preclinical model for adenoid cystic carcinoma of the salivary gland identifies regorafenib as a potential therapeutic drug
title_sort multiplex preclinical model for adenoid cystic carcinoma of the salivary gland identifies regorafenib as a potential therapeutic drug
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595986/
https://www.ncbi.nlm.nih.gov/pubmed/28900283
http://dx.doi.org/10.1038/s41598-017-11764-2
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