Organotypic models of patient-specific tumours are revolutionizing our understanding of cancer heterogeneity and its implications for personalized medicine. These advancements are, in part, attributed to the ability of organoid models to stably preserve genetic, proteomic, morphological and pharmacotypic features of the parent tumour in vitro, while also offering unprecedented genomic and environmental manipulation. Despite recent innovations in organoid protocols, current techniques for cancer organoid culture are inherently uncontrolled and irreproducible, owing to several non-standardized facets including cancer tissue sources and subsequent processing, medium formulations, and animal-derived three-dimensional matrices. Given the potential for cancer organoids to accurately recapitulate the intra- and intertumoral biological heterogeneity associated with patient-specific cancers, eliminating the undesirable technical variability accompanying cancer organoid culture is necessary to establish reproducible platforms that accelerate translatable insights into patient care. Here we describe the current challenges and recent multidisciplinary advancements and opportunities for standardizing next-generation cancer organoid systems. This Review summarizes limitations in the current techniques used for patient-derived cancer organoid culture and highlights recent advancements and future opportunities for their standardization.
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Paracelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, Austria
Tech Univ Munich, Inst Humangenet, Munich, GermanyParacelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, Austria
Wortmann, Saskia B.
Spenger, Johannes
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Paracelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, AustriaParacelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, Austria
Spenger, Johannes
Preisel, Martin
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Paracelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, AustriaParacelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, Austria
Preisel, Martin
Koch, Johannes
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Paracelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, AustriaParacelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, Austria
Koch, Johannes
Rauscher, Christian
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Paracelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, AustriaParacelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, Austria
Rauscher, Christian
Bader, Ingrid
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Paracelsus Med Privatuniv, Div Klin Genet, Univ Klin Kinder & Jugendheilkunde, Salzburg, AustriaParacelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, Austria
Bader, Ingrid
Mayr, Johannes A.
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Paracelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, AustriaParacelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, Austria
Mayr, Johannes A.
Sperl, Wolfgang
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Paracelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, AustriaParacelsus Med Privatuniv, Univ Klin Kinder & Jugendheilkunde, Salzburg, Austria
Sperl, Wolfgang
PADIATRIE UND PADOLOGIE,
2018,
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: 278
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