4.6 Review

Are In Vitro Human Blood-Brain-Tumor-Barriers Suitable Replacements for In Vivo Models of Brain Permeability for Novel Therapeutics?

Journal

CANCERS
Volume 13, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/cancers13050955

Keywords

blood brain barrier; permeability; neurovascular unit; brain microvascular endothelial cells; induced pluripotent stem cells; tight junctions; transendothelial electrical resistance; brain cancer; glioblastoma; diffuse intrinsic pontine glioma

Categories

Funding

  1. THE MARK HUGHES FOUNDATION [HMRI 1357]
  2. Matt Callander Beanie for Brain Cancer Hunter Medical Research Institute (HMRI) Fellowship - Mark Hughes Foundation [HMRI 780]
  3. Mark Hughes Foundation Innovation Grant [HMRI 1096]

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This study demonstrates that in vitro models comprising a variety of cell types can partially replicate the physiological ability of in vivo models to assess brain permeability of novel drugs for brain cancer. This information will be helpful in guiding the development and use of in vitro models for novel therapeutics of unknown permeability for brain cancer, ultimately reducing the need for animal use in medical research.
Simple Summary Brain cancers are a devastating disease with no cure. The aim of the study was to determine whether in vitro models can replace in vivo models to assess the brain permeability of novel drugs for brain cancer. Using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses guidelines, our systematic review reveals that microfluidic-based in vitro models comprising stem cell-derived endothelial cells, and primary astrocytes, pericytes and neurons can, in part, replicate the physiological ability of in vivo models to mimic patient permeability data. This information will guide the development and use of in vitro models for novel therapeutics of unknown permeability for brain cancer. Background: High grade gliomas (HGG) are incapacitating and prematurely fatal diseases. To overcome the poor prognosis, novel therapies must overcome the selective and restricted permeability of the blood-brain barrier (BBB). This study critically evaluated whether in vitro human normal BBB and tumor BBB (BBTB) are suitable alternatives to gold standard in vivo models to determine brain permeability. Methods: A systematic review utilizing the PRISMA guidelines used English and full-text articles from the past 5 years in the PubMed, Embase, Medline and Scopus databases. Experimental studies employing human cell lines were included. Results: Of 1335 articles, the search identified 24 articles for evaluation after duplicates were removed. Eight in vitro and five in vivo models were identified with the advantages and disadvantages compared within and between models, and against patient clinical data where available. The greatest in vitro barrier integrity and stability, comparable to in vivo and clinical permeability data, were achieved in the presence of all cell types of the neurovascular unit: endothelial cells, astrocytes/glioma cells, pericytes and neurons. Conclusions: In vitro co-culture BBB models utilizing stem cell-derived or primary cells are a suitable proxy for brain permeability studies in order to reduce animal use in medical research.

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