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Establishment of a ccRCC patient-derived chick chorioallantoic membrane model for drug testing

Clear cell renal cell carcinoma (ccRCC) is an aggressive subtype of renal cell carcinoma accounting for the majority of deaths in kidney cancer patients. Advanced ccRCC has a high mortality rate as most patients progress and develop resistance to currently approved targeted therapies, highlighting t...

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Autores principales: Charbonneau, Martine, Harper, Kelly, Brochu-Gaudreau, Karine, Perreault, Alexis, McDonald, Patrick P., Ekindi-Ndongo, Nadia, Jeldres, Claudio, Dubois, Claire M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582329/
https://www.ncbi.nlm.nih.gov/pubmed/36275794
http://dx.doi.org/10.3389/fmed.2022.1003914
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author Charbonneau, Martine
Harper, Kelly
Brochu-Gaudreau, Karine
Perreault, Alexis
McDonald, Patrick P.
Ekindi-Ndongo, Nadia
Jeldres, Claudio
Dubois, Claire M.
author_facet Charbonneau, Martine
Harper, Kelly
Brochu-Gaudreau, Karine
Perreault, Alexis
McDonald, Patrick P.
Ekindi-Ndongo, Nadia
Jeldres, Claudio
Dubois, Claire M.
author_sort Charbonneau, Martine
collection PubMed
description Clear cell renal cell carcinoma (ccRCC) is an aggressive subtype of renal cell carcinoma accounting for the majority of deaths in kidney cancer patients. Advanced ccRCC has a high mortality rate as most patients progress and develop resistance to currently approved targeted therapies, highlighting the ongoing need for adequate drug testing models to develop novel therapies. Current animal models are expensive and time-consuming. In this study, we investigated the use of the chick chorioallantoic membrane (CAM), a rapid and cost-effective model, as a complementary drug testing model for ccRCC. Our results indicated that tumor samples from ccRCC patients can be successfully cultivated on the chick chorioallantoic membrane (CAM) within 7 days while retaining their histopathological characteristics. Furthermore, treatment of ccRCC xenografts with sunitinib, a tyrosine kinase inhibitor used for the treatment of metastatic RCC, allowed us to evaluate differential responses of individual patients. Our results indicate that the CAM model is a complementary in vivo model that allows for rapid and cost-effective evaluation of ccRCC patient response to drug therapy. Therefore, this model has the potential to become a useful platform for preclinical evaluation of new targeted therapies for the treatment of ccRCC.
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spelling pubmed-95823292022-10-21 Establishment of a ccRCC patient-derived chick chorioallantoic membrane model for drug testing Charbonneau, Martine Harper, Kelly Brochu-Gaudreau, Karine Perreault, Alexis McDonald, Patrick P. Ekindi-Ndongo, Nadia Jeldres, Claudio Dubois, Claire M. Front Med (Lausanne) Medicine Clear cell renal cell carcinoma (ccRCC) is an aggressive subtype of renal cell carcinoma accounting for the majority of deaths in kidney cancer patients. Advanced ccRCC has a high mortality rate as most patients progress and develop resistance to currently approved targeted therapies, highlighting the ongoing need for adequate drug testing models to develop novel therapies. Current animal models are expensive and time-consuming. In this study, we investigated the use of the chick chorioallantoic membrane (CAM), a rapid and cost-effective model, as a complementary drug testing model for ccRCC. Our results indicated that tumor samples from ccRCC patients can be successfully cultivated on the chick chorioallantoic membrane (CAM) within 7 days while retaining their histopathological characteristics. Furthermore, treatment of ccRCC xenografts with sunitinib, a tyrosine kinase inhibitor used for the treatment of metastatic RCC, allowed us to evaluate differential responses of individual patients. Our results indicate that the CAM model is a complementary in vivo model that allows for rapid and cost-effective evaluation of ccRCC patient response to drug therapy. Therefore, this model has the potential to become a useful platform for preclinical evaluation of new targeted therapies for the treatment of ccRCC. Frontiers Media S.A. 2022-10-06 /pmc/articles/PMC9582329/ /pubmed/36275794 http://dx.doi.org/10.3389/fmed.2022.1003914 Text en Copyright © 2022 Charbonneau, Harper, Brochu-Gaudreau, Perreault, McDonald, Ekindi-Ndongo, Jeldres and Dubois. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Medicine
Charbonneau, Martine
Harper, Kelly
Brochu-Gaudreau, Karine
Perreault, Alexis
McDonald, Patrick P.
Ekindi-Ndongo, Nadia
Jeldres, Claudio
Dubois, Claire M.
Establishment of a ccRCC patient-derived chick chorioallantoic membrane model for drug testing
title Establishment of a ccRCC patient-derived chick chorioallantoic membrane model for drug testing
title_full Establishment of a ccRCC patient-derived chick chorioallantoic membrane model for drug testing
title_fullStr Establishment of a ccRCC patient-derived chick chorioallantoic membrane model for drug testing
title_full_unstemmed Establishment of a ccRCC patient-derived chick chorioallantoic membrane model for drug testing
title_short Establishment of a ccRCC patient-derived chick chorioallantoic membrane model for drug testing
title_sort establishment of a ccrcc patient-derived chick chorioallantoic membrane model for drug testing
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9582329/
https://www.ncbi.nlm.nih.gov/pubmed/36275794
http://dx.doi.org/10.3389/fmed.2022.1003914
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