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Organotypic culture assays for murine and human primary and metastatic-site tumors

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Cancer invasion and metastasis are challenging to study in vivo since they occur deep inside the body over extended time periods. Organotypic 3D culture of fresh tumor tissue enables convenient… Click to show full abstract

Cancer invasion and metastasis are challenging to study in vivo since they occur deep inside the body over extended time periods. Organotypic 3D culture of fresh tumor tissue enables convenient real-time imaging, genetic and microenvironmental manipulation and molecular analysis. Here, we provide detailed protocols to isolate and culture heterogenous organoids from murine and human primary and metastatic site tumors. The time required to isolate organoids can vary based on the tissue and organ type but typically takes <7 h. We describe a suite of assays that model specific aspects of metastasis, including proliferation, survival, invasion, dissemination and colony formation. We also specify comprehensive protocols for downstream applications of organotypic cultures that will allow users to (i) test the role of specific genes in regulating various cellular processes, (ii) distinguish the contributions of several microenvironmental factors and (iii) test the effects of novel therapeutics. This protocol describes the isolation and 3D culture of organoids from fresh murine or human primary and metastatic tumor tissue and provides instructions for real-time imaging, genetic and microenvironmental manipulation and molecular analysis.

Keywords: organotypic culture; primary metastatic; human primary; metastatic site; murine human; culture

Journal Title: Nature Protocols
Year Published: 2020

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