TY - JOUR T1 - Differential Proteomic Analysis of Hepatocellular Carcinomas from <em>Ppp2r5d</em> Knockout Mice and Normal (Knockout) Livers JF - Cancer Genomics - Proteomics JO - Cancer Genomics Proteomics SP - 669 LP - 685 DO - 10.21873/cgp.20222 VL - 17 IS - 6 AU - CAROLINE LAMBRECHT AU - GABRIELA BOMFIM FERREIRA AU - JUDIT DOMÈNECH OMELLA AU - LOUIS LIBBRECHT AU - RITA DE VOS AU - RITA DERUA AU - CHANTAL MATHIEU AU - LUT OVERBERGH AU - ETIENNE WAELKENS AU - VEERLE JANSSENS Y1 - 2020/11/01 UR - http://cgp.iiarjournals.org/content/17/6/669.abstract N2 - Background: Hepatocellular carcinoma (HCC) is the major type of primary liver cancer. Mice lacking the tumor-suppressive protein phosphatase 2A subunit B56δ (Ppp2r5d) spontaneously develop HCC, correlating with increased c-MYC oncogenicity. Materials and Methods: We used two-dimensional difference gel electrophoresis-coupled matrix-assisted laser desorption/ionization time-of-flight mass spectrometry to identify differential proteomes of livers from wild-type, non-cancerous and HCC-affected B56δ knockout mice. Results: A total of 23 proteins were differentially expressed/regulated in liver between wild-type and non-cancerous knockout mice, and 119 between non-cancerous and HCC knockout mice (‘cancer proteins’). Overlap with our reported differential transcriptome data was poor. Overall, 56% of cancer proteins were reported before in HCC proteomics studies; 44% were novel. Gene Ontology analysis revealed cancer proteins mainly associated with liver metabolism (18%) and mitochondria (15%). Ingenuity Pathway Analysis identified ‘cancer’ and ‘gastrointestinal disease’ as top hits. Conclusion: We identified several proteins for further exploration as novel potential HCC biomarkers, and independently underscored the relevance of Ppp2r5d knockout mice as a valuable hepatocarcinogenesis model. ER -