bioRxivCancer Biology
Sodium accumulation in breast cancer predicts malignancy and treatment response
A. D. James, T. K. Leslie, J. D. Kaggie, L. Wiggins, L. Patten, J. M. O'Duinn, S. Langer, M.-C. Labarthe, F. Riemer, G. Baxter, M. A. McLean, F. J. Gilbert, A. J. Kennerley, W. J. Brackenbury
Abstract
Breast cancer is the leading cause of cancer-related death in women worldwide. Development of novel noninvasive diagnostic and predictive pathophysiological biomarkers would represent a significant clinical improvement. Here, we explored the utility of non-invasive 23Na MRI to profile tumour physiology using preclinical mouse models of breast cancer. We establish that tissue Na+ concentration ([Na+]) is elevated vs non-tumour regions across multiple different tumour models. Ex vivo SBFI fluorescence imaging corroborated that this elevation in tumour [Na+] is due to increased intracellular [Na+]. Effective treatment with cytotoxic chemotherapy reduced tumour tissue [Na+], but was not detected by 1H diffusion-weighted imaging (DWI). Moreover, combining 23Na MRI and DWI measurements enabled superior classification accuracy of tumour vs non-tumour regions compared to either parameter alone. Quantification of breast tumour tissue [Na+] using 23Na MRI thus represents a novel, accurate, non-invasive diagnostic and predictive imaging biomarker.
- organism: mouse
- assay: imaging
- research focus: differential expression
- research focus: cell type annotation
- approach: experimental assay
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