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Using PDX for Preclinical Cancer Drug Discovery: The Evolving Field

The ability to create patient derived xenografts (PDXs) has evolved considerably from the breakthrough of the development of immune compromised mice. How researchers in drug discovery have utilized PDX of certain cancer types has also changed from traditionally selecting a few models to profile a dr...

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Detalles Bibliográficos
Autor principal: Williams, Juliet A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867567/
https://www.ncbi.nlm.nih.gov/pubmed/29498669
http://dx.doi.org/10.3390/jcm7030041
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author Williams, Juliet A.
author_facet Williams, Juliet A.
author_sort Williams, Juliet A.
collection PubMed
description The ability to create patient derived xenografts (PDXs) has evolved considerably from the breakthrough of the development of immune compromised mice. How researchers in drug discovery have utilized PDX of certain cancer types has also changed from traditionally selecting a few models to profile a drug, to opting to assess inter-tumor response heterogeneity by screening across a broad range of tumor models, and subsequently to enable clinical stratification strategies. As with all models and methodologies, imperfections with this approach are apparent, and our understanding of the fidelity of these models continues to expand. To date though, they are still viewed as one of the most faithful modeling systems in oncology. Currently, there are many efforts ongoing to increase the utility and translatability of PDXs, including introducing a human immune component to enable immunotherapy studies.
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spelling pubmed-58675672018-04-09 Using PDX for Preclinical Cancer Drug Discovery: The Evolving Field Williams, Juliet A. J Clin Med Review The ability to create patient derived xenografts (PDXs) has evolved considerably from the breakthrough of the development of immune compromised mice. How researchers in drug discovery have utilized PDX of certain cancer types has also changed from traditionally selecting a few models to profile a drug, to opting to assess inter-tumor response heterogeneity by screening across a broad range of tumor models, and subsequently to enable clinical stratification strategies. As with all models and methodologies, imperfections with this approach are apparent, and our understanding of the fidelity of these models continues to expand. To date though, they are still viewed as one of the most faithful modeling systems in oncology. Currently, there are many efforts ongoing to increase the utility and translatability of PDXs, including introducing a human immune component to enable immunotherapy studies. MDPI 2018-03-02 /pmc/articles/PMC5867567/ /pubmed/29498669 http://dx.doi.org/10.3390/jcm7030041 Text en © 2018 by the author. 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
Williams, Juliet A.
Using PDX for Preclinical Cancer Drug Discovery: The Evolving Field
title Using PDX for Preclinical Cancer Drug Discovery: The Evolving Field
title_full Using PDX for Preclinical Cancer Drug Discovery: The Evolving Field
title_fullStr Using PDX for Preclinical Cancer Drug Discovery: The Evolving Field
title_full_unstemmed Using PDX for Preclinical Cancer Drug Discovery: The Evolving Field
title_short Using PDX for Preclinical Cancer Drug Discovery: The Evolving Field
title_sort using pdx for preclinical cancer drug discovery: the evolving field
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5867567/
https://www.ncbi.nlm.nih.gov/pubmed/29498669
http://dx.doi.org/10.3390/jcm7030041
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