4.7 Article

Altered Elemental Distribution in Male Rat Brain Tissue as a Predictor of Glioblastoma Multiforme Growth-Studies Using SR-XRF Microscopy

Journal

Publisher

MDPI
DOI: 10.3390/ijms23020703

Keywords

glioblastoma multiforme (GBM); animal models of GBM; multi-elemental analysis of rat brain; synchrotron X-ray fluorescence microscopy; U87mg; T98g

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Glioblastoma multiforme (GBM) is a malignant brain tumor with limited treatment options. Animal models are commonly used to study the pathology of GBM and evaluate the efficacy and safety of therapies. In this study, synchrotron radiation-based X-ray fluorescence microscopy was used to investigate elemental changes in the rat brain with glioblastoma. The results showed that elemental changes were strongly correlated with the regions of tumor growth, providing insights into the pathogenesis and progression of GBM and potential biomarkers for its extension.
Glioblastoma multiforme (GBM) is a particularly malignant primary brain tumor. Despite enormous advances in the surgical treatment of cancer, radio- and chemotherapy, the average survival of patients suffering from this cancer does not usually exceed several months. For obvious ethical reasons, the search and testing of the new drugs and therapies of GBM cannot be carried out on humans, and for this purpose, animal models of the disease are most often used. However, to assess the efficacy and safety of the therapy basing on these models, a deep knowledge of the pathological changes associated with tumor development in the animal brain is necessary. Therefore, as part of our study, the synchrotron radiation-based X-ray fluorescence microscopy was applied for multi-elemental micro-imaging of the rat brain in which glioblastoma develops. Elemental changes occurring in animals after the implantation of two human glioma cell lines as well as the cells taken directly from a patient suffering from GBM were compared. Both the extent and intensity of elemental changes strongly correlated with the regions of glioma growth. The obtained results showed that the observation of elemental anomalies accompanying tumor development within an animal's brain might facilitate our understanding of the pathogenesis and progress of GBM and also determine potential biomarkers of its extension. The tumors appearing in a rat's brain were characterized by an increased accumulation of Fe and Se, whilst the tissue directly surrounding the tumor presented a higher accumulation of Cu. Furthermore, the results of the study allow us to consider Se as a potential elemental marker of GBM progression.

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