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de Geus, Susanna W. L.; Boogerd, Leonora S. F.; Swijnenburg, Rutger-Jan; Mieog, J. Sven D.; Tummers, Willemieke S. F. J.; Prevoo, Hendrica A. J. M.; Sier, Cornelis F. M.; Morreau, Hans; Bonsing, Bert A.; van de Velde, Cornelis J. H.; Vahrmeijer, Alexander L.; Kuppen, Peter J. K.
Molecular imaging and biology, 12/2016, Letnik: 18, Številka: 6Journal Article
Purpose The purpose of this study was to identify suitable molecular targets for tumor-specific imaging of pancreatic adenocarcinoma. Procedures The expression of eight potential imaging targets was assessed by the target selection criteria (TASC)—score and immunohistochemical analysis in normal pancreatic tissue ( n = 9), pancreatic ( n = 137), and periampullary ( n = 28) adenocarcinoma. Results Integrin α v β 6 , carcinoembryonic antigen (CEA), epithelial growth factor receptor (EGFR), and urokinase plasminogen activator receptor (uPAR) showed a significantly higher (all p < 0.001) expression in pancreatic adenocarcinoma compared to normal pancreatic tissue and were confirmed by the TASC score as promising imaging targets. Furthermore, these biomarkers were expressed in respectively 88 %, 71 %, 69 %, and 67 % of the pancreatic adenocarcinoma patients. Conclusions The results of this study show that integrin α v β 6 , CEA, EGFR, and uPAR are suitable targets for tumor-specific imaging of pancreatic adenocarcinoma.
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JCR | SNIP | JCR | SNIP | JCR | SNIP | JCR | SNIP |
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Povezave do osebnih bibliografij avtorjev | Povezave do podatkov o raziskovalcih v sistemu SICRIS |
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Vir: Osebne bibliografije
in: SICRIS
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