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1 Department of Biomedical NMR and National Bio NMR Facility,
2 Department of Biotechnology and Molecular Medicine, A. I. Virtanen Institute for Molecular Sciences, University of Kuopio, Kuopio, Finland;
3 Center for Magnetic Resonance Research, Department of Radiology, and Cancer Center, University of Minnesota, Minneapolis, Minnesota;
4 School of Biological Sciences, University of Manchester, Manchester, United Kingdom
Magnetic resonance imaging relaxation times, T1
and Carr-Purcell T2 (CP-T2), were measured in a glioma herpes simplex virus-thymidine kinase gene therapy model. In treated tumors with >50% cell death by histology, T1
and CP-T2 measured with short spacing (
CP) between centers of adiabatic refocusing pulses showed similar enhanced sensitivity to cytotoxic cell damage over CP-T2 measured with long
CP (long-
CP T2: 54.3 ± 0.7 and 55.4 ± 1.2 ms, P = 0.30; short-
CP T2: 61.3 ± 1.0 and 64.2 ± 1.1 ms, P < 0.05 before and day 2 of treatment, respectively). Without treatment, long-
CP T2 provided the most pronounced contrast between tumor and normal cerebral tissue. These data demonstrate that endogenous T2 contrast can be modulated and extended in a manner likely to be clinically important.
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M. I. Kettunen, A. Sierra, M. J. Narvainen, P. K. Valonen, S. Yla-Herttuala, R. A. Kauppinen, and O. H. J. Grohn Low Spin-Lock Field T1 Relaxation in the Rotating Frame as a Sensitive MR Imaging Marker for Gene Therapy Treatment Response in Rat Glioma Radiology, March 1, 2007; 243(3): 796 - 803. [Abstract] [Full Text] [PDF] |
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