Abstract |
The diagnosis of early and aggressive types of cancer is important for providing effective cancer therapy. Cancer-induced fibrin clots exist only within lesions. Previously, we developed a monoclonal antibody (clone 102-10) that recognizes insoluble fibrin but not fibrinogen or soluble fibrin and confirmed that fibrin clots form continuously in various cancers. Here, we describe the development of a Fab fragment probe of clone 102-10 for tumour imaging. The distribution of 102-10 Fab was investigated in genetically engineered mice bearing pancreatic ductal adenocarcinoma (PDAC), and its effect on blood coagulation was examined. Immunohistochemical and ex vivo imaging revealed that 102-10 Fab was distributed selectively in fibrin clots in PDAC tumours 3 h after injection and that it disappeared from the body after 24 h. 102-10 Fab had no influence on blood coagulation or fibrinolysis. Tumour imaging using anti- fibrin Fab may provide a safe and effective method for the diagnosis of invasive cancers by detecting fibrin clots in tumour stroma.
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Authors | Toshifumi Obonai, Hirobumi Fuchigami, Fumiaki Furuya, Naoyuki Kozuka, Masahiro Yasunaga, Yasuhiro Matsumura |
Journal | Scientific reports
(Sci Rep)
Vol. 6
Pg. 23613
(Mar 24 2016)
ISSN: 2045-2322 [Electronic] England |
PMID | 27009516
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Antibodies, Monoclonal
- Fibrin
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Topics |
- Animals
- Antibodies, Monoclonal
(administration & dosage, pharmacology)
- Carcinoma, Pancreatic Ductal
(diagnosis, genetics, metabolism)
- Early Detection of Cancer
- Fibrin
(immunology)
- Genetic Engineering
- Humans
- Mice
- Mutation
- Neoplasms, Experimental
- Pancreatic Neoplasms
(genetics, metabolism)
- Tumor Microenvironment
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