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pmid:33870183
Urinary Metabolomic and Proteomic Analyses in a Mouse Model of Prostatic Inflammation.
Pingli Wei · Ling Hao · Fengfei Ma · Qing Yu · Amanda Rae Buchberger · Sanghee Lee · Wade Bushman · Lingjun Li
Urine (Amsterdam, Netherlands) · 2019 doi:10.1016/j.urine.2020.05.002
Paper
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Experiment
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Data
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Analysis
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Execution
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Complete file
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Since prostatic inflammation is one of its etiologies, it is plausible that urinary metabolite and protein biomarkers could be identified and used to diagnose inflammation-induced LUTS. We characterized the urine metabolome and proteome in a mouse model of bacterial-induced prostatic inflammation. Mass Spectrometry (MS)-based multi-omics analysis was employed to discover urinary protein and metabolite-based biomarkers. The investigation of isobaric dimethylated leucine (DiLeu) labeling on metabolites allowed metabolomics and proteomics analysis on the same liquid chromatography (LC)-MS platform. In total, 143 amine-containing metabolites and 1058 urinary proteins were identified and quantified (data are available via ProteomeXchange with identifier PXD018023); among them, 14 metabolites and 168 proteins were significantly changed by prostatic inflammation. Five metabolic pathways and four inflammation-related biological processes were potentially disrupted. By comparing our findings with urinary biomarkers identified in a mouse model of genetic-induced prostate inflammation and with those previously found to be associated with LUTS in older men, we identified creatine, haptoglobin, immunoglobulin kappa constant and polymeric Ig receptor as conserved biomarkers for prostatic inflammation associated with LUTS. 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