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The insulin-like growth factor 2 (<i>IGF2</i>) mRNA binding protein IMP2 (IGF2BP2) is an oncogenic protein known to be overexpressed in different tumor types. Pancreatic cancer is a very lethal cancer that requires early diagnosis and new treatment options. The aim of our study was to investigate the role of IMP2 in the initiation and progression of pancreatic ductal adenocarcinoma (PDAC). <i>IMP2</i> was significantly overexpressed in a human precursor (PanIN) lesions suggesting IMP2 as a marker for early stages of PDAC. In a PDAC cohort of matched normal and tumor samples <i>IMP2</i> showed overexpression in tumor tissues compared with normal pancreatic tissue. Strict correlation analysis (threshold <i>R</i>² &gt; 0.75) revealed 22 genes highly positively and 9 genes highly negatively correlating with <i>IMP2</i>. Besides genes involved in the inhibition of apoptosis (<i>Bcl-XL</i>), especially factors involved in ubiquitination were strongly correlated with <i>IMP2</i> expression: <i>SMURF1</i> and <i>FBXO45</i>. Moreover, protein kinase C (PKC) signaling pathway was distinctly affected: <i>DXS1179E</i> encoding PKC iota, PKC substrate <i>PLEK2</i>, and inositol triphosphate receptor <i>IP3R3</i> were positively correlated with <i>IMP2</i> expression. Besides tumor initiation, IMP2 also seemed to have an impact on tumor progression. TGF-&#946; treatment of Panc-1 pancreatic cancer cells to induce epithelial-mesenchymal transition (EMT) was accompanied by increased <i>IMP2</i> expression. EMT is important for cancer cells to gain migratory and invasive potential, which is essential for metastasis. Concordantly, circulating tumor cells showed higher <i>IMP2</i> levels as compared with normal tissue from tumor origin and with normal hematological cells. Accordingly, IMP2 protein levels correlated with poor survival. In conclusion, as IMP2 seems to promote tumor progression of PDAC, it might be an interesting diagnostic and prognostic marker as well as a novel target for the treatment of PDAC.