Please use this identifier to cite or link to this item: https://doi.org/10.1007/s00216-010-4055-3
Title: Metabolic footprinting of tumorigenic and nontumorigenic uroepithelial cells using two-dimensional gas chromatography time-of-flight mass spectrometry
Authors: Pasikanti, K.K.
Norasmara, J.
Cai, S.
Mahendran, R. 
Esuvaranathan, K.
Ho, P.C. 
Chan, E.C.Y. 
Keywords: Bladder cancer
Metabolic footprinting
Metabolic profiling
Metabolomics
Metabonomics
Two-dimensional gas chromatography time-of-flight mass spectrometry
Issue Date: Oct-2010
Citation: Pasikanti, K.K., Norasmara, J., Cai, S., Mahendran, R., Esuvaranathan, K., Ho, P.C., Chan, E.C.Y. (2010-10). Metabolic footprinting of tumorigenic and nontumorigenic uroepithelial cells using two-dimensional gas chromatography time-of-flight mass spectrometry. Analytical and Bioanalytical Chemistry 398 (3) : 1285-1293. ScholarBank@NUS Repository. https://doi.org/10.1007/s00216-010-4055-3
Abstract: In this study, gas chromatography mass spectrometry (GC-MS) and two-dimensional gas chromatography time-of-flight mass spectrometry (GC×GC-TOFMS) were employed for the metabolic footprinting of a pair of immortalized human uroepithelial cells namely HUC-1 (nontumorigenic) and HUC T-2 (tumorigenic). Both HUC-1 and HUC T-2 cell lines were cultivated in 1 mL of Ham's F-12 media. Subsequent to 48 h of incubation, 200 μL of cell culture supernatant was protein-precipitated using 1.7 mL of methanol and an aliquot of 1.5 mL of the mixture was separated, dried, trimethylsilyl-derivatized, and analyzed using GC-MS and GC×GC-TOFMS. Metabolic profiles were analyzed using multivariate data analysis techniques to evaluate the changes of the metabolomes. Both GC-MS and GC×GC-TOFMS analyses showed distinct differences in metabolic phenotypes of the normal and tumorigenic human bladder cells (partial least squares-discriminant analysis (PLS-DA) of GC×GC-TOFMS data; two latent variables, R 2 X = 0.418, R 2 Y = 0.977 and Q 2 (cumulative) = 0.852). Twenty metabolites were identified as being statistically different between the two cell types. These metabolites revealed that several key metabolic pathways were perturbed in tumorigenic urothelial cells as compared to the normal cells. Application of GC×GC-TOFMS offered several advantages compared to classical one-dimensional GC-MS which include enhanced chromatographic resolution (without increase in analytical run time), increase in sensitivity, improved identification of metabolites, and also separation of reagent artifacts from the metabolite peaks. Our results reinforced the advantages of GC×GC-TOFMS and the role of metabolomics in characterizing bladder cancer biology using in vitro cell culture models. © 2010 Springer-Verlag.
Source Title: Analytical and Bioanalytical Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/108616
ISSN: 16182642
DOI: 10.1007/s00216-010-4055-3
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