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Cultivating Ex Vivo Patient-Derived Glioma Organoids Using a Tissue Chopper.
Alsalkini, Marah; Cibulková, Veronika; Breun, Maria; Kessler, Almuth F; Schulz, Tim; Cattaneo, Andrea; Wipplinger, Christoph; Hübner, Julian; Ernestus, Ralf-Ingo; Nerreter, Thomas; Monoranu, Camelia M; Hagemann, Carsten; Löhr, Mario; Nickl, Vera.
Afiliação
  • Alsalkini M; Section Experimental Neurosurgery, Department of Neurosurgery, University Hospital Würzburg.
  • Cibulková V; Section Experimental Neurosurgery, Department of Neurosurgery, University Hospital Würzburg.
  • Breun M; Department of Neurosurgery, University Hospital Würzburg.
  • Kessler AF; Department of Neurosurgery, University Hospital Würzburg.
  • Schulz T; Department of Neurosurgery, University Hospital Würzburg.
  • Cattaneo A; Department of Neurosurgery, University Hospital Würzburg.
  • Wipplinger C; Department of Neurosurgery, University Hospital Würzburg.
  • Hübner J; Department of Hematology, University Hospital Würzburg.
  • Ernestus RI; Department of Neurosurgery, University Hospital Würzburg.
  • Nerreter T; Department of Hematology, University Hospital Würzburg.
  • Monoranu CM; Department of Neuropathology, Institute of Pathology, University Hospital Würzburg.
  • Hagemann C; Section Experimental Neurosurgery, Department of Neurosurgery, University Hospital Würzburg.
  • Löhr M; Department of Neurosurgery, University Hospital Würzburg.
  • Nickl V; Department of Neurosurgery, University Hospital Würzburg; Nickl_V@ukw.de.
J Vis Exp ; (203)2024 Jan 19.
Article em En | MEDLINE | ID: mdl-38314829
ABSTRACT
Glioblastoma, IDH-wild type, CNS WHO grade 4 (GBM) is a primary brain tumor associated with poor patient survival despite aggressive treatment. Developing realistic ex vivo models remain challenging. Patient-derived 3-dimensional organoid (PDO) models offer innovative platforms that capture the phenotypic and molecular heterogeneity of GBM, while preserving key characteristics of the original tumors. However, manual dissection for PDO generation is time-consuming, expensive and can result in a number of irregular and unevenly sized PDOs. This study presents an innovative method for PDO production using an automated tissue chopper. Tumor samples from four GBM and one astrocytoma, IDH-mutant, CNS WHO grade 2 patients were processed manually as well as using the tissue chopper. In the manual approach, the tumor material was dissected using scalpels under microscopic control, while the tissue chopper was employed at three different angles. Following culture on an orbital shaker at 37 °C, morphological changes were evaluated using bright field microscopy, while proliferation (Ki67) and apoptosis (CC3) were assessed by immunofluorescence after 6 weeks. The tissue chopper method reduced almost 70% of the manufacturing time and resulted in a significantly higher PDOs mean count compared to the manually processed tissue from the second week onwards (week 2 801 vs. 601, P = 0.018; week 3 1105 vs. 771, P = 0.032; and week 41195 vs. 784, P < 0.01). Quality assessment revealed similar rates of tumor-cell apoptosis and proliferation for both manufacturing methods. Therefore, the automated tissue chopper method offers a more efficient approach in terms of time and PDO yield. This method holds promise for drug- or immunotherapy-screening of GBM patients.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Astrocitoma / Neoplasias Encefálicas / Glioblastoma / Glioma Tipo de estudo: Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: J Vis Exp Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Astrocitoma / Neoplasias Encefálicas / Glioblastoma / Glioma Tipo de estudo: Guideline / Prognostic_studies Limite: Humans Idioma: En Revista: J Vis Exp Ano de publicação: 2024 Tipo de documento: Article