학술논문

In Vivo Measurements of Tumor Metabolism and Growth after Administration of Enzastaurin Using Small Animal FDG Positron Emission Tomography.
Document Type
Article
Source
Journal of Oncology. 2009, p1-8. 8p. 3 Color Photographs, 1 Chart, 2 Graphs.
Subject
*TUMOR growth
*PROTEIN kinases
*LABORATORY mice
*XENOGRAFTS
*HEMATOLOGIC agents
*POSITRON emission tomography
*CALIPERS
*GLYCOGENOLYSIS
*ANTINEOPLASTIC agents
Language
ISSN
1687-8450
Abstract
Background. The use of 2-[18F]fluoro-2-deoxy-D-glucose ([18F]FDG) may help to establish the antitumor activity of enzastaurin, a novel protein kinase C-beta II (PKC-βII) inhibitor, in mouse xenografts. Methods. The hematologic cell line RAJI and the solid tumor cell line U87MG were each implanted in NOD/SCID mice. Standard tumor growth measurements and [18F]FDG PET imaging were performed weekly for up to three weeks after tumor implantation and growth. Results. Concomitant with caliper measurements, [18F]FDG PET imaging was performed to monitor glucosemetabolism. Heterogeneity of glucose uptake in various areas of the tumors was observed after vehicle or enzastaurin treatment. This heterogeneity may limit the use of [18F]FDG PET imaging to measure enzastaurin-associated changes in xenograft tumors. Conclusion. [18F]FDG PET imaging technique does not correlate with standard caliper assessments in xenografts to assess the antitumor activity of enzastaurin. Future studies are needed to determine the use of [18F]FDG PET imaging in preclinical models. [ABSTRACT FROM AUTHOR]