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  • Development of a metabolomic radiation signature in urine from patients undergoing total body irradiation.

Development of a metabolomic radiation signature in urine from patients undergoing total body irradiation.

Radiation research (2014-03-29)
Evagelia C Laiakis, Tytus D Mak, Sebastien Anizan, Sally A Amundson, Christopher A Barker, Suzanne L Wolden, David J Brenner, Albert J Fornace
ABSTRACT

The emergence of the threat of radiological terrorism and other radiological incidents has led to the need for development of fast, accurate and noninvasive methods for detection of radiation exposure. The purpose of this study was to extend radiation metabolomic biomarker discovery to humans, as previous studies have focused on mice. Urine was collected from patients undergoing total body irradiation at Memorial Sloan-Kettering Cancer Center prior to hematopoietic stem cell transplantation at 4-6 h postirradiation (a single dose of 1.25 Gy) and 24 h (three fractions of 1.25 Gy each). Global metabolomic profiling was obtained through analysis with ultra performance liquid chromatography coupled to time-of-flight mass spectrometry (TOFMS). Prior to further analyses, each sample was normalized to its respective creatinine level. Statistical analysis was conducted by the nonparametric Kolmogorov-Smirnov test and the Fisher's exact test and markers were validated against pure standards. Seven markers showed distinct differences between pre- and post-exposure samples. Of those, trimethyl-l-lysine and the carnitine conjugates acetylcarnitine, decanoylcarnitine and octanoylcarnitine play an important role in the transportation of fatty acids across mitochondria for subsequent fatty acid β-oxidation. The remaining metabolites, hypoxanthine, xanthine and uric acid are the final products of the purine catabolism pathway, and high levels of excretion have been associated with increased oxidative stress and radiation induced DNA damage. Further analysis revealed sex differences in the patterns of excretion of the markers, demonstrating that generation of a sex-specific metabolomic signature will be informative and can provide a quick and reliable assessment of individuals in a radiological scenario. This is the first radiation metabolomics study in human urine laying the foundation for the use of metabolomics in biodosimetry and providing confidence in biomarker identification based on the overlap between animal models and humans.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
4-Nitrobenzoic acid, 98%
Sigma-Aldrich
L-Lysine, crystallized, ≥98.0% (NT)
Sigma-Aldrich
4-Nitrobenzoic acid, purum, ≥98.0% (HPLC)
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Hypoxanthine, powder, BioReagent, suitable for cell culture
Sigma-Aldrich
Hypoxanthine, ≥99.0%
Sigma-Aldrich
L-Lysine, ≥98% (TLC)
Didanosine impurity A,, European Pharmacopoeia (EP) Reference Standard
Supelco
L-Lysine, analytical standard
Lysine hydrochloride, European Pharmacopoeia (EP) Reference Standard
Supelco
L-Lysine hydrochloride solution, 100 mM amino acid in 0.1 M HCl, analytical standard
Sigma-Aldrich
L-Lysine monohydrochloride, BioUltra, ≥99.5% (AT)
Sigma-Aldrich
Xanthine, BioUltra, ≥99%
Sigma-Aldrich
L-Lysine monohydrochloride, reagent grade, ≥98% (HPLC)
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O-Acetyl-L-carnitine hydrochloride, ≥99% (titration), powder
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Debrisoquine sulfate
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Uric acid, BioXtra, ≥99% (HPLC)
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Creatinine, anhydrous, ≥98%
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Xanthine, ≥99.5% (HPLC), purified by recrystallization
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L-Lysine monohydrochloride, from non-animal source, meets EP, JP, USP testing specifications, suitable for cell culture, 98.5-101.0%
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Xanthine, ≥99%
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L-Lysine monohydrochloride, SAJ special grade, ≥99.0%
Sigma-Aldrich
Uric acid, ≥99%, crystalline
Supelco
L-Lysine monohydrochloride, certified reference material, TraceCERT®, Manufactured by: Sigma-Aldrich Production GmbH, Switzerland
Supelco
L-Lysine monohydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material
Supelco
Creatinine, Pharmaceutical Secondary Standard; Certified Reference Material