A systematic review of normal tissue neurovascular unit damage following brain irradiation—Factors affecting damage severity and timing of effects

Author:

Nakkazi Annet12,Forster Duncan2,Whitfield Gillian A34,Dyer Douglas P51,Dickie Ben R12ORCID

Affiliation:

1. Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Group, The University of Manchester , Manchester, UK

2. Faculty of Biology, Medicine, and Health, Division of Informatics, Imaging, and Data Sciences, School of Health Sciences, The University of Manchester , Manchester, UK

3. Division of Cancer Sciences, Manchester Cancer Research Centre, Manchester Academic Health Science Centre, The University of Manchester , Manchester, UK

4. The Christie NHS Foundation Trust , Manchester, UK

5. Wellcome Centre for Cell-Matrix Research, Lydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine, and Health, Manchester Academic Health Science Centre, The University of Manchester , Manchester, UK

Abstract

Abstract Background Radiotherapy is key in the treatment of primary and secondary brain tumors. However, normal tissue is inevitably irradiated, causing toxicity and contributing to cognitive dysfunction. The relative importance of vascular damage to cognitive decline is poorly understood. Here, we systematically review the evidence for radiation-induced damage to the entire neurovascular unit (NVU), particularly focusing on establishing the factors that influence damage severity, and timing and duration of vascular effects relative to effects on neural tissue. Methods Using PubMed and Web of Science, we searched preclinical and clinical literature published between January 1, 1970 and December 1, 2022 and evaluated factors influencing NVU damage severity and timing of NVU effects resulting from ionizing radiation. Results Seventy-two rodents, 4 canines, 1 rabbit, and 5 human studies met inclusion criteria. Radiation increased blood-brain barrier (BBB) permeability, reduced endothelial cell number and extracellular matrix proteoglycans, reduced tight junction proteins, upregulated cellular adhesion molecule expression, reduced activity of glucose and BBB efflux transporters and activated glial cells. In the brain parenchyma, increased metalloproteinases 2 and 9 levels, demyelination, cell death, and inhibited differentiation were observed. Effects on the vasculature and neural compartment were observed across acute, delayed, and late timepoints, and damage extent was higher with low linear energy transfer radiation, higher doses, lower dose rates, broader beams, and in the presence of a tumor. Conclusions Irradiation of normal brain tissue leads to widespread and varied impacts on the NVU. Data indicate that vascular damage is in most cases an early effect that does not quickly resolve. More studies are needed to confirm sequence of damages, and mechanisms that lead to cognitive dysfunction.

Funder

Cancer Research UK

Royal Society

Wellcome Trust

Publisher

Oxford University Press (OUP)

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