The Alcatraz‐Strategy: a roadmap to break the connectivity barrier in malignant brain tumours

Author:

Schneider Matthias12ORCID,Potthoff Anna‐Laura12ORCID,Karpel‐Massler Georg3,Schuss Patrick4,Siegelin Markus D.5,Debatin Klaus‐Michael6,Duffau Hugues78,Vatter Hartmut12,Herrlinger Ulrich29ORCID,Westhoff Mike‐Andrew6

Affiliation:

1. Department of Neurosurgery University Hospital Bonn Germany

2. Brain Tumour Translational Research Group University Hospital Bonn Germany

3. Department of Neurosurgery University Medical Center Ulm Germany

4. Department of Neurosurgery BG Klinikum Unfallkrankenhaus Berlin gGmbH Germany

5. Department of Pathology and Cell Biology Columbia University Irving Medical Center New York NY USA

6. Department of Pediatrics and Adolescent Medicine University Medical Center Ulm Germany

7. Department of Neurosurgery, Gui de Chauliac Hospital Montpellier University Medical Center France

8. Team “Plasticity of Central Nervous System, Stem Cells and Glial Tumors,” National Institute for Health and Medical Research (INSERM), U1191 Laboratory, Institute of Functional Genomics University of Montpellier France

9. Division of Clinical Neuro‐Oncology, Department of Neurology University Hospital Bonn Germany

Abstract

In recent years, the discovery of functional and communicative cellular tumour networks has led to a new understanding of malignant primary brain tumours. In this review, the authors shed light on the diverse nature of cell‐to‐cell connections in brain tumours and propose an innovative treatment approach to address the detrimental connectivity of these networks. The proposed therapeutic outlook revolves around three main strategies: (a) supramarginal resection removing a substantial portion of the communicating tumour cell front far beyond the gadolinium‐enhancing tumour mass, (b) morphological isolation at the single cell level disrupting structural cell‐to‐cell contacts facilitated by elongated cellular membrane protrusions known as tumour microtubes (TMs), and (c) functional isolation at the single cell level blocking TM‐mediated intercellular cytosolic exchange and inhibiting neuronal excitatory input into the malignant network. We draw an analogy between the proposed therapeutic outlook and the Alcatraz Federal Penitentiary, where inmates faced an impassable sea barrier and experienced both spatial and functional isolation within individual cells. Based on current translational efforts and ongoing clinical trials, we propose the Alcatraz‐Strategy as a promising framework to tackle the harmful effects of cellular brain tumour networks.

Funder

Deutsche Krebshilfe

Publisher

Wiley

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