Cancer Research 09 AM Call for Abstracts
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 35, 785-790, March 1, 1975]
© 1975 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wassenaar, W.
Right arrow Articles by Batty, H. P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wassenaar, W.
Right arrow Articles by Batty, H. P.

Glucose Analogs as Potential Diagnostic Tracers for Brain Tumors1

Willem Wassenaar2, Charles H. Tator3 and Helen P. Batty

Division of Neurosurgery, Department of Surgery, University of Toronto, Toronto, Ontario, Canada

No tumor-specific tracer has yet been found for the detection of brain tumors by external scintiscanning. Glucose is a substrate in high demand by almost all tumors, and therefore an investigation was undertaken into the potential value of glucose and its analogs as tracers for brain tumors. The compounds studied were D-[1-3H]glucose, D-[1-14C]glucose, [3H]3-O-methyl-D-glucose and L-[1-14C]glucose. The tracers were injected i.v. into C57BL/6J mice carrying a transplantable s.c. ependymoblastoma. At specific time intervals after injection, mice were sacrificed and the radioactivity of 6 tissues including tumor and brain were assayed by means of an automated combustion technique and liquid scintillation counting.

Tumor uptake, expressed as percentage mean body concentration, was 60% for 2 of the tracers, and 92 and 143%, respectively, for 2 others. Brain uptake was over 130% mean body concentration, with 3 of the 4 tracers studied. With L-glucose, brain uptake was only 15.4% mean body concentration, and a maximum tumor-to-brain ratio of 9.5 was achieved. The very high tumor uptake achieved with two of these carbohydrates demonstrates that a carbohydrate analog may be found that shows high tumor specificity and uptake, and that may be useful for external scintiscanning.

1 This work was supported by Ontario Cancer Treatment and Research Foundation Grant 247.

2 Research Fellow of the Medical Research Council of Canada.

3 To whom reprint requests should be addressed, at Division of Neurosurgery, Room 7317, Medical Sciences Building, University of Toronto, Toronto, Ontario, M5S 1A8, Canada.

Received 4/ 4/74. Accepted 12/ 6/74.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1975 by the American Association for Cancer Research.