a) Scaling up of resonant structures to enable imaging larger objects for pO2. We have achieved, in prior years the capability of studying tumor bearing mice for oxygen status. Image formation and reconstruction techniques were developed and implemented to obtain images with useful spatial and temporal resolutions. Such efforts will provide experience to translate this imaging modality to study humans, at least local regions to obtain important physiological information. We have designed, constructed, tested and successfully implemented a four-channel coil array which quadrupled the volume which can accommodate larger objects the size of rat/rabbit. This size makes studies of tumors such as head and neck, breast, and prostate. b) Accelerated imaging of tumor oxygenation using EPRI to allow monitoring dynamics of tumor oxygen. Most imaging techniques using tracers for hypoxia and PET imaging obtain a static picture of the tumor oxygen status. But many pre-clinical studies in experimental animals suggest that oxygen supply in tumors is a dynamic phenomenon with regions of chronic hypoxia and regions with cycling hypoxia. EPRI, intrinsically being a technique which uses a paramagnetic tracer on which oxygen molecule imposes a contrast, allows obtaining maps of oxygen without actually consuming it as in the case of an electrode or reports indirectly as in PET. To allow examining the dynamics of tumor oxygenation, the temporal resolution of EPRI has been significantly improved using a model based reconstruction approach allowing us to take a 3-D snap shot in under 1 min. c) With the improvements in imaging of tumor oxygen dynamics, it was possible to use EPR imaging to synergize the efficacy of the hypoxia activated prodrug TH-302 with prior administration of pyruvate to increase hypoxia. Pyruvate, which is used to image metabolism has also been found to increase transiently tumor hypoxia, as detected by EPRI. Since TH-302 is a hypoxia selective toxin, increasing hypoxia with pyruvate may increase its efficacy. EPRI was used to determine the treatment schedule.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Investigator-Initiated Intramural Research Projects (ZIA)
Project #
1ZIABC010476-13
Application #
9153577
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
13
Fiscal Year
2015
Total Cost
Indirect Cost
Name
Basic Sciences
Department
Type
DUNS #
City
State
Country
Zip Code
Matsumoto, Ken-Ichiro; Kishimoto, Shun; Devasahayam, Nallathamby et al. (2018) EPR-based oximetric imaging: a combination of single point-based spatial encoding and T1 weighting. Magn Reson Med 80:2275-2287
Matsumoto, Ken-Ichiro; Hyodo, Fuminori; Mitchell, James B et al. (2018) Effect of body temperature on the pharmacokinetics of a triarylmethyl-type paramagnetic contrast agent used in EPR oximetry. Magn Reson Med 79:1212-1218
Kishimoto, Shun; Krishna, Murali C; Khramtsov, Valery V et al. (2018) In Vivo Application of Proton-Electron Double-Resonance Imaging. Antioxid Redox Signal 28:1345-1364
Scroggins, Bradley T; Matsuo, Masayuki; White, Ayla O et al. (2018) Hyperpolarized [1-13C]-Pyruvate Magnetic Resonance Spectroscopic Imaging of Prostate Cancer In Vivo Predicts Efficacy of Targeting the Warburg Effect. Clin Cancer Res 24:3137-3148
Matsumoto, Ken-Ichiro; Mitchell, James B; Krishna, Murali C (2018) Comparative studies with EPR and MRI on the in vivo tissue redox status estimation using redox-sensitive nitroxyl probes: influence of the choice of the region of interest. Free Radic Res 52:248-255
Matsumoto, Shingo; Kishimoto, Shun; Saito, Keita et al. (2018) Metabolic and Physiologic Imaging Biomarkers of the Tumor Microenvironment Predict Treatment Outcome with Radiation or a Hypoxia-Activated Prodrug in Mice. Cancer Res 78:3783-3792
Matsuo, Masayuki; Kawai, Tatsuya; Kishimoto, Shun et al. (2018) Co-imaging of the tumor oxygenation and metabolism using electron paramagnetic resonance imaging and 13-C hyperpolarized magnetic resonance imaging before and after irradiation. Oncotarget 9:25089-25100
Kishimoto, Shun; Matsumoto, Ken-Ichiro; Saito, Keita et al. (2018) Pulsed Electron Paramagnetic Resonance Imaging: Applications in the Studies of Tumor Physiology. Antioxid Redox Signal 28:1378-1393
Takakusagi, Yoichi; Kishimoto, Shun; Naz, Sarwat et al. (2018) Radiotherapy Synergizes with the Hypoxia-Activated Prodrug Evofosfamide: In Vitro and In Vivo Studies. Antioxid Redox Signal 28:131-140
Yasui, Hironobu; Kawai, Tatsuya; Matsumoto, Shingo et al. (2017) Quantitative imaging of pO2 in orthotopic murine gliomas: hypoxia correlates with resistance to radiation. Free Radic Res 51:861-871

Showing the most recent 10 out of 21 publications