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Comprehensive Metabolomics and Lipidomics Profiling of Prostate Cancer Tissue Reveals Metabolic Dysregulations Associated with Disease Development

代谢组学 脂类学 前列腺癌 代谢途径 代谢组 生物 脂质代谢 嘌呤代谢 新陈代谢 计算生物学 生物化学 生物信息学 癌症 癌症研究 化学 遗传学
作者
Ana Rita Lima,Márcia Carvalho,Susana S. Aveiro,Tânia Melo,M. Rosário M. Domingues,Catarina Macedo‐Silva,Nuno Coimbra,Cármen Jerónimo,Rui Henrique,Maria de Lourdes Bastos,Paula Guedes de Pinho,Joana Pinto
出处
期刊:Journal of Proteome Research [American Chemical Society]
卷期号:21 (3): 727-739 被引量:16
标识
DOI:10.1021/acs.jproteome.1c00754
摘要

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.
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