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Xenograft and organoid model systems in cancer research

Patient‐derived tumour xenografts and tumour organoids have become important preclinical model systems for cancer research. Both models maintain key features from their parental tumours, such as genetic and phenotypic heterogeneity, which allows them to be used for a wide spectrum of applications. I...

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Autores principales: Bleijs, Margit, van de Wetering, Marc, Clevers, Hans, Drost, Jarno
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6670015/
https://www.ncbi.nlm.nih.gov/pubmed/31282586
http://dx.doi.org/10.15252/embj.2019101654
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author Bleijs, Margit
van de Wetering, Marc
Clevers, Hans
Drost, Jarno
author_facet Bleijs, Margit
van de Wetering, Marc
Clevers, Hans
Drost, Jarno
author_sort Bleijs, Margit
collection PubMed
description Patient‐derived tumour xenografts and tumour organoids have become important preclinical model systems for cancer research. Both models maintain key features from their parental tumours, such as genetic and phenotypic heterogeneity, which allows them to be used for a wide spectrum of applications. In contrast to patient‐derived xenografts, organoids can be established and expanded with high efficiency from primary patient material. On the other hand, xenografts retain tumour–stroma interactions, which are known to contribute to tumorigenesis. In this review, we discuss recent advances in patient‐derived tumour xenograft and tumour organoid model systems and compare their promises and challenges as preclinical models in cancer research.
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spelling pubmed-66700152019-08-06 Xenograft and organoid model systems in cancer research Bleijs, Margit van de Wetering, Marc Clevers, Hans Drost, Jarno EMBO J Review Patient‐derived tumour xenografts and tumour organoids have become important preclinical model systems for cancer research. Both models maintain key features from their parental tumours, such as genetic and phenotypic heterogeneity, which allows them to be used for a wide spectrum of applications. In contrast to patient‐derived xenografts, organoids can be established and expanded with high efficiency from primary patient material. On the other hand, xenografts retain tumour–stroma interactions, which are known to contribute to tumorigenesis. In this review, we discuss recent advances in patient‐derived tumour xenograft and tumour organoid model systems and compare their promises and challenges as preclinical models in cancer research. John Wiley and Sons Inc. 2019-07-08 2019-08-01 /pmc/articles/PMC6670015/ /pubmed/31282586 http://dx.doi.org/10.15252/embj.2019101654 Text en © 2019 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Bleijs, Margit
van de Wetering, Marc
Clevers, Hans
Drost, Jarno
Xenograft and organoid model systems in cancer research
title Xenograft and organoid model systems in cancer research
title_full Xenograft and organoid model systems in cancer research
title_fullStr Xenograft and organoid model systems in cancer research
title_full_unstemmed Xenograft and organoid model systems in cancer research
title_short Xenograft and organoid model systems in cancer research
title_sort xenograft and organoid model systems in cancer research
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6670015/
https://www.ncbi.nlm.nih.gov/pubmed/31282586
http://dx.doi.org/10.15252/embj.2019101654
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