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Detecting tumor response to treatment using hyperpolarized 13C magnetic resonance imaging and spectroscopy

✍ Scribed by Day, Sam E; Kettunen, Mikko I; Gallagher, Ferdia A; Hu, De-En; Lerche, Mathilde; Wolber, Jan; Golman, Klaes; Ardenkjaer-Larsen, Jan Henrik; Brindle, Kevin M


Book ID
109933056
Publisher
Nature Publishing Group
Year
2007
Tongue
English
Weight
546 KB
Volume
13
Category
Article
ISSN
1078-8956

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✦ Synopsis


Measurements of early tumor responses to therapy have been shown, in some cases, to predict treatment outcome. We show in lymphoma-bearing mice injected intravenously with hyperpolarized [1-13 C]pyruvate that the lactate dehydrogenasecatalyzed flux of 13 C label between the carboxyl groups of pyruvate and lactate in the tumor can be measured using 13 C magnetic resonance spectroscopy and spectroscopic imaging, and that this flux is inhibited within 24 h of chemotherapy. The reduction in the measured flux after drug treatment and the induction of tumor cell death can be explained by loss of the coenzyme NAD(H) and decreases in concentrations of lactate and enzyme in the tumors. The technique could provide a new way to assess tumor responses to treatment in the clinic.


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## Abstract We show here that hyperpolarized [1‐^13^C]pyruvate can be used to detect treatment response in a glioma tumor model; a tumor type where detection of response with ^18^fluoro‐2‐deoxyglucose, using positron emission tomography, is limited by the high background signals from normal brain t