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Metabolic profiling of serum in patients with cartilage tumours using 1 H-NMR spectroscopy: A pilot study

Authors :
Romeo Técualt-Gómez
Angel E. Bañuelos-Hernández
Nury Pérez-Hernández
Liliana López-Garrido
Elvia Becerra-Martínez
Jorge Quiroz-Williams
Elizabeth Pérez-Hernández
Armando Ariza-Castolo
Source :
Magnetic Resonance in Chemistry. 58:65-76
Publication Year :
2019
Publisher :
Wiley, 2019.

Abstract

Cartilage-forming lesions include tumours that can vary in severity from benign enchondromas to high-grade malignant chondrosarcomas. Chondrosarcoma is the second most frequent malignant bone tumour, accounting for 20-30% of all malignant bone neoplasms. Surgery is the standard treatment for cartilage tumours (CTs); however, their incidental diagnosis and the difficult differentiation of low-grade lesions like chondrosarcoma grade I from benign entities like enchondroma are challenges for clinical management. In this sense, the search for circulating biomarkers for early detection and prognosis is an ongoing interest. Targeted metabolomics is a powerful tool that can propose potential biomarkers in biological fluids as well as help to discover disturbed metabolic pathways to reveal tumour pathogenesis. In this context, the aim of this study was to investigate the 1 H nuclear magnetic resonance metabolomic serum profile of patients with CTs contrasted with healthy controls. Forty-one metabolites were identified and quantified; the multivariate statistical methods principal component analysis and partial least squares discriminant analysis reveal a clear separation of the CT group, that is, the differential metabolites that were involved in two main metabolic pathways: the taurine and hypotaurine metabolism and synthesis and degradation of ketone bodies. Our results represent preliminary work for emergent serum-based diagnostics or prognostic methods for patients with chondrogenic tumours.

Details

ISSN :
07491581
Volume :
58
Database :
OpenAIRE
Journal :
Magnetic Resonance in Chemistry
Accession number :
edsair.doi...........118d708b204414f645bfa355395c09bc
Full Text :
https://doi.org/10.1002/mrc.4925