Generation of glioblastoma patient-derived organoids and mouse brain orthotopic xenografts for drug screening
Robust patient-derived platforms that recapitulate the cellular and molecular fingerprints of glioblastoma are crucial for developing effective therapies. Here, we describe a chemically defined protocol for 3D culture and propagation of glioblastoma in 3D gliospheres, patient-derived organoids (PDOs...
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Veröffentlicht in: | STAR protocols 2021-03, Vol.2 (1), p.100345-100345, Article 100345 |
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Sprache: | eng |
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Zusammenfassung: | Robust patient-derived platforms that recapitulate the cellular and molecular fingerprints of glioblastoma are crucial for developing effective therapies. Here, we describe a chemically defined protocol for 3D culture and propagation of glioblastoma in 3D gliospheres, patient-derived organoids (PDOs), mouse brain orthotopic xenografts (PDOXs), and downstream drug and immunofluorescence assays. This simple-to-follow protocol allows assessing drug sensitivity, on-target activity, and combined drug synergy. Promising therapies can then be validated in PDOXs for translation in precision medicine oncology trials.
For complete details on the use and execution of this protocol, please refer to Chadwick et al. (2020) and Patrizii et al. (2018).
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•Reproducible generation of 3D cultured glioblastoma patient-derived organoids (PDOs)•Gliospheres and PDOs can be propagated and cryopreserved for downstream applications•Engrafted cells are imaged with MRI/BLI in mouse brain orthotopic xenografts•PDOs are used to assess synergy between drug combinations for combined targeted therapy
Robust patient-derived platforms that recapitulate the cellular and molecular fingerprints of glioblastoma are crucial for developing effective therapies. Here, we describe a chemically defined protocol for 3D culture and propagation of glioblastoma in 3D gliospheres, patient-derived organoids (PDOs), mouse brain orthotopic xenografts (PDOXs), and downstream drug and immunofluorescence assays. This simple-to-follow protocol allows assessing drug sensitivity, on-target activity, and combined drug synergy. Promising therapies can then be validated in PDOXs for translation in precision medicine oncology trials. |
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ISSN: | 2666-1667 2666-1667 |
DOI: | 10.1016/j.xpro.2021.100345 |