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      Molecular Imaging of the Tumor Microenvironment reveals the Relationship between Tumor Oxygenation, Glucose Uptake and Glycolysis in Pancreatic Ductal Adenocarcinoma

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          Abstract

          Molecular imaging approaches for metabolic and physiological imaging of tumors have become important for treatment planning and response monitoring. However, the relationship between the physiological and metabolic aspects of tumors is not fully understood. Here, we developed new hyperpolarized MRI and EPR imaging procedures that allow more direct assessment of tumor glycolysis and oxygenation status quantitatively. We investigated the spatial relationship between hypoxia, glucose uptake, and glycolysis in three human pancreatic ductal adenocarcinoma tumor xenografts with differing physiological and metabolic characteristics. At the bulk tumor level, there was a strong positive correlation between 18F-FDG PET and lactate production, while pO 2 was inversely related to lactate production and 18F-FDG uptake. However, metabolism was not uniform throughout the tumors, and the whole tumor results masked different localizations that became apparent while imaging. 18F-FDG uptake negatively correlated with pO 2 in the center of the tumor and positively correlated with pO 2 on the periphery. In contrast to pO 2 and 18F-FDG uptake, lactate dehydrogenase activity was distributed relatively evenly throughout the tumor. The heterogeneity revealed by each measure suggests a multimodal molecular imaging approach can improve tumor characterization, potentially leading to better prognostics in cancer treatment.

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          Author and article information

          Journal
          2984705R
          2786
          Cancer Res
          Cancer Res.
          Cancer research
          0008-5472
          1538-7445
          11 April 2020
          03 April 2020
          01 June 2020
          01 December 2020
          : 80
          : 11
          : 2087-2093
          Affiliations
          [1 ]Radiation Biology Branch, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States
          [2 ]Clinical Monitoring Research Program Directorate, Frederick National Laboratory for Cancer Research, National Cancer Institute, Frederick, MD, United States
          [3 ]Molecular Imaging Program, Center for Cancer Research, National Cancer Institute, National Institutes of Health, Bethesda, MD, United States
          Author notes
          [†]

          These authors contributed equally to this work.

          [* ]Corresponding author: Murali C. Krishna, Ph.D., Radiation Biology Branch, Center for Cancer Research, National Cancer Institute, Building 10, Room B3B35, NIH, Bethesda, MD 20892-1002, Phone: 240-858-3089, Fax: 240-541-4528, murali@ 123456helix.nih.gov
          Article
          PMC7272278 PMC7272278 7272278 nihpa1581343
          10.1158/0008-5472.CAN-19-0928
          7272278
          32245793
          7bbb9918-e4e7-4ceb-abd9-e7f3a6a03ba3
          History
          Categories
          Article

          EPR imaging,Tumor Microenvironment,Hyperpolarized MRI,Multimodal Imaging,Molecular Imaging

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