Hyperpolarized C-13 spectroscopic imaging of the TRAMP mouse at 3T-Initial experience

The transgenic adenocarcinoma of mouse prostate (TRAMP) mouse is a well‐studied murine model of prostate cancer with histopathology and disease progression that mimic the human disease. To investigate differences in cellular bioenergetics between normal prostate epithelial cells and prostate tumor c...

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Published inMagnetic resonance in medicine Vol. 58; no. 6; pp. 1099 - 1106
Main Authors Chen, Albert P., Albers, Mark J., Cunningham, Charles H., Kohler, Susan J., Yen, Yi-Fen, Hurd, Ralph E., Tropp, James, Bok, Robert, Pauly, John M., Nelson, Sarah J., Kurhanewicz, John, Vigneron, Daniel B.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.12.2007
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Summary:The transgenic adenocarcinoma of mouse prostate (TRAMP) mouse is a well‐studied murine model of prostate cancer with histopathology and disease progression that mimic the human disease. To investigate differences in cellular bioenergetics between normal prostate epithelial cells and prostate tumor cells, in vivo MR spectroscopic (MRS) studies with non‐proton nuclei, such as 13C, in the TRAMP model would be extremely useful. The recent development of a method for retaining dynamic nuclear polarization (DNP) in solution permits high signal‐to‐noise ratio (SNR) 13C MRI or MRSI data to be obtained following injection of a hyperpolarized 13C agent. In this transgenic mouse study, this method was applied using a double spin‐echo (DSE) pulse sequence with a small‐tip‐angle excitation RF pulse, hyperbolic‐secant refocusing pulses, and a flyback echo‐planar readout trajectory for fast (10–14 s) MRSI of 13C pyruvate (pyr) and its metabolic products at 0.135 cm3 nominal spatial resolution. Elevated 13C lactate (lac) was observed in both primary and metastatic tumors, demonstrating the feasibility of studying cellular bioenergetics in vivo with DNP hyperpolarized 13C MRSI. Magn Reson Med, 2007. © 2007 Wiley‐Liss, Inc.
Bibliography:istex:17793C49C5393F49759F3C391DB5E03CD5774F9F
ark:/67375/WNG-SB8BKF0C-9
National Institutes of Health - No. R21 EB005363; No. NIH R01 EB007588
UC Discovery/GE Healthcare - No. LSIT 10107
ArticleID:MRM21256
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ISSN:0740-3194
1522-2594
DOI:10.1002/mrm.21256