Life SciencesBiochemistryOncologyCarcinogenesisProtein BiochemistryProteomicsCancer ProteomicsMass Spectrometry-based ProteomicsProtein IdentificationProteomic BiomarkersProteomic ProfilingTumor MarkersCancer Proteome ProfilingIntratumoral Proteomic VariationMass Spectrometry-based Protein IdentificationProtein Analysis In Body FluidsTandem Mass SpectrometryTandem Mass Spectrometry AnalysisTumor Proteome ProfilingTumor Proteomics
BACKGROUND: Urine, as a potential biomarker source among body fluids, can accumulate many early changes in the body due to the lack of mechanisms to maintain a homeostatic state. This study aims to detect early changes in the urinary proteome in a rat liver tumour model. METHODS: The tumour model was established with the Walker-256 carcinosarcoma cell line (W256). Urinary proteins at days 3, 5, 7 and 11 were profiled by liquid chromatography coupled with tandem mass spectrometry (LC-MS/MS). Compared with controls, differential proteins were selected. Associations of differential proteins with cancer were retrieved. RESULTS: At days 3, 5, 7 and 11, five, fifteen, eleven and twelve differential proteins were identified, respectively. Some of the differential proteins were reported to be associated with liver cancer. This differential urinary protein pattern was different from the patterns in W256 subcutaneous, lung metastasis and intracerebral tumour models. CONCLUSIONS: This study demonstrates that (1) early changes in urinary proteins can be found in the rat liver tumour model; (2) urinary proteins can be used to differentiate the same tumour cells grown in different organs.
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