TY - JOUR
T1 - Xenograft and organoid model systems in cancer research
AU - Bleijs, Margit
AU - van de Wetering, Marc
AU - Clevers, Hans
AU - Drost, Jarno
PY - 2019/8/1
Y1 - 2019/8/1
N2 - 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.
AB - 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.
KW - cancer
KW - organoids
KW - preclinical models
KW - tumour heterogeneity
KW - xenografts
U2 - 10.15252/embj.2019101654
DO - 10.15252/embj.2019101654
M3 - Article
C2 - 31282586
SN - 1460-2075
JO - The EMBO Journal Vol. 38 | No. 15 1 August 2019
JF - The EMBO Journal Vol. 38 | No. 15 1 August 2019
ER -