| Literature DB >> 34813334 |
Ana Rita Lima1,2, Márcia Carvalho1,2,3,4, Susana S Aveiro5,6, Tânia Melo5,7, M Rosário Domingues5,7, Catarina Macedo-Silva8, Nuno Coimbra9,10, Carmen Jerónimo8,9, Rui Henrique8,9,10, Maria de Lourdes Bastos1,2, Paula Guedes de Pinho1,2, Joana Pinto1,2.
Abstract
Prostate cancer (PCa) is a global health problem that affects millions of men every year. In the past decade, metabolomics and related subareas, such as lipidomics, have demonstrated an enormous potential to identify novel mechanisms underlying PCa development and progression, providing a good basis for the development of new and more effective therapies and diagnostics. In this study, a multiplatform metabolomics and lipidomics approach, combining untargeted mass spectrometry (MS) and nuclear magnetic resonance (NMR)-based techniques, was applied to PCa tissues to investigate dysregulations associated with PCa development, in a cohort of 40 patients submitted to radical prostatectomy for PCa. Results revealed significant alterations in the levels of 26 metabolites and 21 phospholipid species in PCa tissue compared with adjacent nonmalignant tissue, suggesting dysregulation in 13 metabolic pathways associated with PCa development. The most affected metabolic pathways were amino acid metabolism, nicotinate and nicotinamide metabolism, purine metabolism, and glycerophospholipid metabolism. A clear interconnection between metabolites and phospholipid species participating in these pathways was observed through correlation analysis. Overall, these dysregulations may reflect the reprogramming of metabolic responses to produce high levels of cellular building blocks required for rapid PCa cell proliferation.Entities:
Keywords: lipidomics; metabolic pathways; metabolomics; prostate cancer; tissue
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Year: 2021 PMID: 34813334 DOI: 10.1021/acs.jproteome.1c00754
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466