Glioblastoma Tissue Slice Tandem-Cultures for Quantitative Evaluation of Inhibitory Effects on Invasion and Growth.

Pim-1 STAT3 ex vivo model glioblastoma tissue slice co-cultures tumor invasion tumor xenografts

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
21 Sep 2020
Historique:
received: 31 07 2020
revised: 16 09 2020
accepted: 17 09 2020
entrez: 24 9 2020
pubmed: 25 9 2020
medline: 25 9 2020
Statut: epublish

Résumé

Glioblastomas (GBMs) are the most malignant brain tumors and are essentially incurable even after extensive surgery, radiotherapy, and chemotherapy, mainly because of extensive infiltration of tumor cells into the adjacent normal tissue. Thus, the evaluation of novel drugs in malignant glioma treatment requires sophisticated ex vivo models that approach the authentic interplay between tumor and host environment while avoiding extensive in vivo studies in animals. This paper describes the standardized setup of an organotypic brain tissue slice tandem-culture system, comprising of normal brain tissue from adult mice and tumor tissue from human glioblastoma xenografts, and explore its utility for assessing inhibitory effects of test drugs. The microscopic analysis of vertical sections of the slice tandem-cultures allows for the simultaneous assessment of (i) the invasive potential of single cells or cell aggregates and (ii) the space occupying growth of the bulk tumor mass, both contributing to malignant tumor progression. The comparison of tissue slice co-cultures with spheroids vs. tissue slice tandem-cultures using tumor xenograft slices demonstrates advantages of the xenograft tandem approach. The direct and facile application of test drugs is shown to exert inhibitory effects on bulk tumor growth and/or tumor cell invasion, and allows their precise quantitation. In conclusion, we describe a straightforward ex vivo system mimicking the in vivo situation of the tumor mass and the normal brain in GBM patients. It reduces animal studies and allows for the direct and reproducible application of test drugs and the precise quantitation of their effects on the bulk tumor mass and on the tumor's invasive properties.

Identifiants

pubmed: 32967361
pii: cancers12092707
doi: 10.3390/cancers12092707
pmc: PMC7564455
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : AI24/13-1, KO1898/9-1
Organisme : Deutsche Krebshilfe
ID : 111616

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Auteurs

Vasile Sidorcenco (V)

Rudolf-Boehm-Institute for Pharmacology and Toxicology, Clinical Pharmacology, Medical Faculty, University of Leipzig, 04109 Leipzig, Germany.
Rudolf-Boehm-Institute for Pharmacology and Toxicology, Medical Faculty, University of Leipzig, 04109 Leipzig, Germany.
Department of Neurosurgery, Jena University Hospital, 07747 Jena, Germany.

Luisa Krahnen (L)

Rudolf-Boehm-Institute for Pharmacology and Toxicology, Clinical Pharmacology, Medical Faculty, University of Leipzig, 04109 Leipzig, Germany.
Rudolf-Boehm-Institute for Pharmacology and Toxicology, Medical Faculty, University of Leipzig, 04109 Leipzig, Germany.

Marion Schulz (M)

Rudolf-Boehm-Institute for Pharmacology and Toxicology, Clinical Pharmacology, Medical Faculty, University of Leipzig, 04109 Leipzig, Germany.

Janina Remy (J)

Experimental Neurosurgery, Department of Neurosurgery, Neuroscience Center, Goethe University Hospital and German Cancer Consortium (DKTK), Partner Site Frankfurt, 60438 Frankfurt am Main, Germany.

Donat Kögel (D)

Experimental Neurosurgery, Department of Neurosurgery, Neuroscience Center, Goethe University Hospital and German Cancer Consortium (DKTK), Partner Site Frankfurt, 60438 Frankfurt am Main, Germany.

Achim Temme (A)

Department of Neurosurgery, Section Experimental Neurosurgery and Tumor Immunology, University Hospital Carl Gustav Carus, Technical University Dresden, 01069 Dresden, Germany.
German Cancer Consortium (DKTK), Partner Site Dresden, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
National Center for Tumor Diseases (NCT), 69120 Heidelberg, Germany.

Ute Krügel (U)

Rudolf-Boehm-Institute for Pharmacology and Toxicology, Medical Faculty, University of Leipzig, 04109 Leipzig, Germany.

Heike Franke (H)

Rudolf-Boehm-Institute for Pharmacology and Toxicology, Medical Faculty, University of Leipzig, 04109 Leipzig, Germany.

Achim Aigner (A)

Rudolf-Boehm-Institute for Pharmacology and Toxicology, Clinical Pharmacology, Medical Faculty, University of Leipzig, 04109 Leipzig, Germany.

Classifications MeSH