In Vivo Measurement of Brain Tissue Response After Irradiation: Comparison of T2 Relaxation, Apparent Diffusion Coefficient, and Electrical Conductivity.

Radiation therapy (RT) has been widely used as a powerful treatment tool to address cancerous tissues because of its ability to control cell growth. Its ionizing radiation damages the DNA of cancerous tissues, leading to cell death. Medical imaging, however, still has limitations regarding the reliability of its assessment of tissue response and in predicting the treatment effect because of its inability to provide contrast information on the gradual, minute tissue changes after RT. A recently developed magnetic resonance (MR)-based conductivity imaging method may provide direct, highly sensitive information on this tissue response because its contrast mechanism is based on the concentration and mobility of ions in intracellular and extracellular spaces. In this feasibility study, we applied T2-weighted, diffusion-weighted, and electrical conductivity imaging to mouse brain, thus, using the MR imaging to map the tissue response after radiation exposure. To evaluate the degree of response, we measured the T2 relaxation, apparent diffusion coefficient (ADC), and electrical conductivity of brain tissues before and after irradiation. The conductivity images, which showed significantly higher sensitivity than other MR imaging methods, indicated that the contrast is distinguishable in different ways at different areas of the brain. Future studies will focus on verifying these results and the long-term evaluation of conductivity changes using various irradiation methods for clinical applications.

Preliminary 19F-MRS Study of Tumor Cell Proliferation with 3'-deoxy-3'-fluorothymidine and Its Metabolite (FLT-MP).

The thymidine analogue 3'-deoxy-3'-[18F]fluorothymidine, or [18F]fluorothymidine ([18F]FLT), is used to measure tumor cell proliferation with positron emission tomography (PET) imaging technology in nuclear medicine. FLT is phosphorylated by thymidine kinase 1 (TK1) and then trapped inside cells; it is not incorporated into DNA. Imaging with 18F-radiolabeled FLT is a noninvasive technique to visualize cellular proliferation in tumors. However, it is difficult to distinguish between [18F]FLT and its metabolites by PET imaging, and quantification has not been attempted using current imaging methods. In this study, we successfully acquired in vivo19F spectra of natural or nonradioactive 3'-deoxy-3'-fluorothymidine ([19F]FLT) and its monophosphate metabolite (FLT-MP) in a tumor xenograft mouse model using 9.4T magnetic resonance imaging (MRI). This preliminary result demonstrates that 19F magnetic resonance spectroscopy (MRS) with FLT is suitable for the in vivo assessment of tumor aggressiveness and for early prediction of treatment response.