Proteomic identification of differentially expressed plasma membrane proteins in renal cell carcinoma by stable isotope labelling of a von Hippel‐Lindau transfectant cell line model |
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Authors: | Vassilis Aggelis Rachel A. Craven Jianhe Peng Patricia Harnden David A. Cairns Eamonn R. Maher Robert Tonge Peter J. Selby Rosamonde E. Banks Professor |
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Affiliation: | 1. Cancer Research UK Clinical Centre, St. James's University Hospital, Leeds, UK;2. Cancer Research UK Renal Molecular Oncology Research Group, University of Birmingham, Birmingham, UK;3. AstraZeneca plc, Alderley Park, Cheshire, UK |
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Abstract: | The von Hippel‐Lindau (VHL) tumour suppressor gene plays a central role in development of clear cell renal cell carcinoma (RCC). Using a cell line pair generated from the VHL‐defective RCC cell line UMRC2 by transfection with vector control or VHL (?/+VHL) and stable isotope labelling with amino acids in cell culture (SILAC) followed by enrichment of plasma membrane proteins by cell surface biotinylation/avidin‐affinity chromatography and analysis by GeLC‐MS/MS, VHL‐associated changes in plasma membrane proteins were analysed. Comparative analysis of ‐/+VHL cells identified 19 differentially expressed proteins which were confirmed by reciprocal SILAC labelling. These included several proteins previously reported to be VHL targets, such as transferrin receptor 1 and the α3 and β1 integrin subunits and novel findings including upregulation of CD166 and CD147 in VHL‐defective cells. Western blotting confirmed these changes and also revealed VHL‐dependent alterations in protein form for CD147 and CD166, which in the case of CD166 was shown to be due to differential glycosylation. Analysis of patient‐matched normal and malignant renal tissues confirmed these differences were also present in vivo in a subset of clear cell RCCs. These results illustrate the potential of this approach for identifying VHL‐dependent proteins that may be important in tumorigenesis. |
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Keywords: | Membrane proteins Renal cancer SILAC VHL |
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