Targeting of surface alpha-enolase inhibits the invasiveness of pancreatic cancer cells

• Published in: Oncotarget 2015-05, Vol.6 (13), p.11098-11113
• Main Authors: Principe, Moitza, Ceruti, Patrizia, Shih, Neng-Yao, Chattaragada, Michelle S, Rolla, Simona, Conti, Laura, Bestagno, Marco, Zentilin, Lorena, Yang, Sheng-Hui, Migliorini, Paola, Cappello, Paola, Burrone, Oscar, Novelli, Francesco
• Format: Article
• Language: English
• Subjects: Animals; Antibodies, Monoclonal - pharmacology; Biomarkers, Tumor - antagonists & inhibitors; Biomarkers, Tumor - genetics; Biomarkers, Tumor - metabolism; Blotting, Western; Carcinoma, Pancreatic Ductal - metabolism; Carcinoma, Pancreatic Ductal - pathology; Carcinoma, Pancreatic Ductal - prevention & control; DNA-Binding Proteins - antagonists & inhibitors; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; Flow Cytometry; Humans; Liver Neoplasms - metabolism; Liver Neoplasms - prevention & control; Liver Neoplasms - secondary; Male; Mice; Mice, Inbred NOD; Mice, SCID; Neoplasm Invasiveness; Pancreatic Neoplasms - metabolism; Pancreatic Neoplasms - pathology; Pancreatic Neoplasms - prevention & control; Phosphopyruvate Hydratase - antagonists & inhibitors; Phosphopyruvate Hydratase - genetics; Phosphopyruvate Hydratase - metabolism; Research Paper; Tumor Cells, Cultured; Tumor Suppressor Proteins - antagonists & inhibitors; Tumor Suppressor Proteins - genetics; Tumor Suppressor Proteins - metabolism; Xenograft Model Antitumor Assays
• ISSN: 1949-2553; 1949-2553
• DOI: 10.18632/oncotarget.3572

Pancreatic Ductal Adenocarcinoma (PDAC) is a highly aggressive malignancy characterized by rapid progression, invasiveness and resistance to treatment. We have previously demonstrated that most PDAC patients have circulating antibodies against the glycolytic enzyme alpha-enolase (ENO1), which correlates with a better response to therapy and survival. ENO1 is a metabolic enzyme, also expressed on the cell surface where it acts as a plasminogen receptor. ENO1 play a crucial role in cell invasion and metastasis by promoting plasminogen activation into plasmin, a serine-protease involved in extracellular matrix degradation. The aim of this study was to investigate the role of ENO1 in PDAC cell invasion. We observed that ENO1 was expressed on the cell surface of most PDAC cell lines. Mouse anti-human ENO1 monoclonal antibodies inhibited plasminogen-dependent invasion of human PDAC cells, and their metastatic spreading in immunosuppressed mice was inhibited. Notably, a single administration of Adeno-Associated Virus (AAV)-expressing cDNA coding for 72/1 anti-ENO1 mAb reduced the number of lung metastases in immunosuppressed mice injected with PDAC cells. Overall, these data indicate that ENO1 is involved in PDAC cell invasion, and that administration of an anti-ENO1 mAb can be exploited as a novel therapeutic option to increase the survival of metastatic PDAC patients.