1H NMR analysis of choline metabolites in fine-needle-aspirate biopsies of breast cancer
Object The relative amounts of choline (Cho), phosphocholine (PC), and glycerophosphocholine (GPC) may be sensitive indicators of breast cancer and the degree of malignancy. Here we implement some simple modifications to a previously developed 1 H NMR analysis of fine-needle-aspirate (FNA) biopsies...
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Published in | Magma (New York, N.Y.) Vol. 26; no. 3; pp. 337 - 343 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer-Verlag
01.06.2013
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Subjects | |
Online Access | Get full text |
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Summary: | Object
The relative amounts of choline (Cho), phosphocholine (PC), and glycerophosphocholine (GPC) may be sensitive indicators of breast cancer and the degree of malignancy. Here we implement some simple modifications to a previously developed
1
H NMR analysis of fine-needle-aspirate (FNA) biopsies designed to yield sufficient spectral resolution of Cho, PC, and GPC for usable relative quantitation of these metabolites.
Materials and methods
FNA biopsies of eighteen breast lesions were examined using our modified procedure for direct
1
H NMR at 400 MHz. Resonances of choline metabolites and potential interferences were fit using the computer program NUTS.
Results
Quantitation of PC, GPC, and Cho relative to each other and to (phospho)creatine was obtained for eleven confirmed cases of infiltrating ductal carcinoma. Reliable results could not be obtained for the remaining cases primarily due to interference from lidocaine anesthetic.
Conclusion
Some simple modifications of a previously developed
1
H NMR analysis of FNAs yielded sufficient spectral resolution of Cho, PC, and GPC to permit usable relative quantitation at 400 MHz. In 9 of the 11 quantified cases the sum of GPC and Cho exceeded 42 % of the total choline-metabolite peak area. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0968-5243 1352-8661 |
DOI: | 10.1007/s10334-012-0349-0 |