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Quantifying Cognitive Decrements Caused by Cranial Radiotherapy
Published on: October 18, 2011
More than a small adult brain: Lessons from chemotherapy-induced cognitive impairment for modelling paediatric brain
Maya R Davies1, Zarina Greenberg2, Dannis G van Vuurden3
1School of Biomedicine, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, SA, Australia; Supportive Oncology Research Group, Precision Cancer Medicine Theme, South Australian Health and Medical Research Institute (SAHMRI), Adelaide, SA, Australia.
Insights
Pediatric cancer treatments can harm the developing brain due to its unique vulnerabilities. More age-specific research and models are crucial for understanding and mitigating neurocognitive side effects in children.
Area of Science:
- Neuroscience
- Developmental Biology
- Pediatric Oncology
Background:
- The developing pediatric brain exhibits high neuroplasticity but immature protective mechanisms, increasing vulnerability to neurotoxic insults.
- Paediatric cancer treatments (surgery, radiation, chemotherapy) can cause significant neurocognitive symptoms in children.
- Current preclinical research predominantly uses adult models, limiting understanding of age-specific treatment effects.
Conclusions:
- Developing age-specific in vitro and in vivo pediatric disease models is essential.
- This research is critical for advancing discovery and ensuring clinically translatable findings for children.
- Addressing the unique neurodevelopmental context is key to mitigating long-term neurocognitive deficits in pediatric cancer survivors.
Abstract:
Childhood is recognised as a period of immense physical and emotional development, and this, in part, is driven by underlying neurophysiological transformations. These neurodevelopmental processes are unique to the paediatric brain and are facilitated by augmented rates of neuroplasticity and expanded neural stem cell populations within neurogenic niches. However, given the immaturity of the developing central nervous system, innate protective mechanisms such as neuroimmune and antioxidant responses are functionally naïve which results in periods of heightened sensitivity to neurotoxic insult. This is highly relevant in the context of paediatric cancer, and in particular, the neurocognitive symptoms associated with treatment, such as surgery, radio- and chemotherapy. The vulnerability of the developing brain may increase susceptibility to damage and persistent symptomology, aligning with reports of more severe neurocognitive dysfunction in children compared to adults. It is therefore surprising, given this intensified neurocognitive burden, that most of the pre-clinical, mechanistic research focuses exclusively on adult populations and extrapolates findings to paediatric cohorts. Given this dearth of age-specific research, throughout this review we will draw comparisons with neurodevelopmental disorders which share comparable pathways to cancer treatment related side-effects. Furthermore, we will examine the unique nuances of the paediatric brain along with the somatic systems which influence neurological function. In doing so, we will highlight the importance of developing in vitro and in vivo paediatric disease models to produce age-specific discovery and clinically translatable research.
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