Magnetic resonance molecular imaging of extradomain B fibronectin enables detection of pancreatic ductal adenocarcinoma metastasis
Autor: | Bryan Scott, David L. Wilson, Yiqiao Liu, Mahdusudhana Gargesha, Peter Qiao, Ryan C. W. Hall, Amita M. Vaidya, Zheng-Rong Lu, Victoria E A Laney, Debashish Roy, Kara L. Gawelek, Hannah Gilmore |
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Rok vydání: | 2022 |
Předmět: |
Pathology
medicine.medical_specialty Magnetic Resonance Spectroscopy Biomedical Engineering Biophysics Metastasis Extracellular matrix Mice Stroma Cell Line Tumor Pancreatic cancer Parenchyma Animals Humans Medicine Radiology Nuclear Medicine and imaging medicine.diagnostic_test business.industry Magnetic resonance imaging medicine.disease Magnetic Resonance Imaging Primary tumor Fibronectins Molecular Imaging Pancreatic Neoplasms Immunohistochemistry business Carcinoma Pancreatic Ductal |
Zdroj: | Magnetic Resonance Imaging. 86:37-45 |
ISSN: | 0730-725X |
DOI: | 10.1016/j.mri.2021.11.008 |
Popis: | Extradomain-B Fibronectin (EDB-FN) is an oncomarker that can be visualized with magnetic resonance molecular imaging (MRMI) to detect pancreatic ductal adenocarcinoma (PDAC) metastasis. In this study, we sought to assess the expression of EDB-FN in clinical samples of PDAC and to evaluate MRMI of PDAC metastasis with an EDB-FN-specific gadolinium-based contrast agent (MT218) in an orthotopic KPC-GFP-Luc mouse model. EDB-FN expression was evaluated in PDAC tissue samples through immunohistochemistry. RNA-Seq data obtained from the GEPIA2 project was evaluated to demonstrate EDB-FN expression in large patient cohorts. FLASH-3D MRI at 3 T of the KPC-GFP-Luc metastasis model was performed following injection of MT218. Tumor enhancement in MR images was correlated to postmortem distribution of KPC-GFP-Luc tumors using fluorescent and bright-field cryo-imaging and anatomical landmarks. EDB-FN immunohistochemical staining scores of human metastatic tumor stroma, (2.17 ± 0.271), metastatic tumor parenchyma (2.08 ± 0.229), primary tumor stroma (1.61 ± 0.26), and primary tumor parenchyma (1.61 ± 0.12) were significantly (p |
Databáze: | OpenAIRE |
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