Dynamin-1 is a potential mediator in Cancer-Related Cognitive Impairment.
Ding Quan NgCasey HudsonTracy NguyenSukesh Kumar GuptaYong Qin KohMunjal M AcharyaAlexandre ChanPublished in: bioRxiv : the preprint server for biology (2024)
Dynamin-1 (DNM1) consolidates memory through synaptic transmission and modulation and has been explored as a therapeutic target in Alzheimer's disease. Through a two-prong approach, this study examined its role in cancer-related cognitive impairment (CRCI) pathogenesis using human and animal models. The human study recruited newly diagnosed, chemotherapy-naïve adolescent and young adult cancer and non-cancer controls to complete a cognitive instrument (FACT-Cog) and blood draws for up to three time points. Concurrently, a syngeneic young-adult WT (C57BL/6 female) mouse model of breast cancer was developed to study DNM1 expression in the brain. Samples from eighty-six participants with 30 adolescent and young adult (AYA) cancer and 56 non-cancer participants were analyzed. DNM1 levels were significantly lower among cancer participants compared to non-cancer prior to treatment. While receiving cancer treatment, cognitively impaired patients were found with a significant downregulation of DNM1, but not among those without impairment. In murine breast cancer-bearing mice receiving chemotherapy, we consistently found a significant decline in DNM1 immunoreactivity in the hippocampal CA1 and CA3 subregions. Observed in both human and animal studies, the downregulation of DNM1 is linked with the onset of CRCI. Future research should explore the potential of DNM1 in CRCI pathogenesis and therapeutics development.
Keyphrases
- papillary thyroid
- young adults
- childhood cancer
- newly diagnosed
- squamous cell
- cognitive impairment
- endothelial cells
- squamous cell carcinoma
- end stage renal disease
- lymph node metastasis
- signaling pathway
- type diabetes
- ejection fraction
- mental health
- climate change
- peritoneal dialysis
- chronic kidney disease
- poor prognosis
- risk assessment
- metabolic syndrome
- adipose tissue
- subarachnoid hemorrhage
- long non coding rna
- induced pluripotent stem cells
- mild cognitive impairment
- case control